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In telecommunication, a Berger code is an unidirectional error detecting code, named after its inventor, J. M. Berger. Berger codes can detect all unidirectional errors. Unidirectional errors are errors that only flip ones into zeroes or only zeroes into ones, such as in asymmetric channels. The check bits of Berger codes are computed by summing all the zeroes in the information word, and expressing that sum in natural binary. If the information word consists of n bits, then the Berger code needs check bits are
"check bits", giving a Berger code of length k+n. (In other words, the k enough to check up to n =2
k
1 information bits). Berger codes can detect any
number of one-to-zero bit-flip errors, as long as no zero-to-one errors occurred in the same code word. Berger codes can detect any number of zero-to-one bit-flip errors, as long as no one-to-zero bit-flip errors occur in the same code word. Berger codes cannot correct any error. Like all unidirectional error detecting codes, Berger codes can also be used in delayinsensitive circuits.
Unidirectional error detection

As stated above, Berger codes detect any
[edit]
number of unidirectional errors. For a , if the only errors that have occurred
given code word
are that some (or all) bits with value 1 have changed to value 0, then this transformation will be detected by the Berger code implementation. To understand why, consider that there are three such cases:
http://en.wikipedia.org/wiki/Berger_code (1 of 5) [2/20/2008 3:41:43 AM]
1. Some 1s bits in the information part of the code word have changed to 0s. 2. Some 1s bits in the check (or redundant code word have changed to 0s. 3. Some 1s bits in both the information and check portions have changed to 0s. For case 1, the number of 0-valued bits in the information section will, by definition of the error, increase. Therefore, our berger check code will be lower than the actual 0-bit-count for the data, and so the check will fail. For case 2, the number of 0-valued bits in the information section have stayed the same, but the value of the check data has changed. Since we know some 1s turned into 0s, but no 0s have turned into 1s (that's how we defined the error model in this case), the encoded binary value of the check data will go down (e.g, from binary 1011 to 1010, or to 1001, or 0011). Since the information data has stayed the same, it has the same number of zeros it did before, and that will no longer match the mutated check value. For case 3, where bits have changed in both the information and the check sections, notice that the number of zeros in the information section has gone up described for case 1, and the binary value stored in the check portion has gone , as ) portion of the
down
, as described for case 2. Therefore, there is no chance that the two will end
up mutating in such a way as to become a different valid code word. A similar analysis can be performed, and is perfectly valid, in the case where the only errors that occur are that some 0-valued bits change to 1. Therefore, if all the errors that occur on a specific codeword all occur in the same direction, these errors will be detected. For the next code word being transmitted (for instance), the errors can go in the opposite direction, and they will still be detected, as long as they all go in the same direction as
each other. Unidirectional errors are common in certain situations. For instance, in flash memory, bits can more easily be programmed to a 0 than can be reset to a 1.
References
[edit]
J. M. Berger, "A note on an error detection code for asymmetric channels",
Information and Control

4, pp. 68-73, March 1961.
, vol
Subhasish Mitra and Edward J. McCluskey, "Which concurrent error detection scheme to choose?", Center for Reliable Computing, Stanford University, 2000.
"Delay-Insensitive Codes -- An Overview" by Tom Verhoeff
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Why the 4 code Genetic Primer Should Have 6 Nucleotide Codes Inosine controls the "degradation" process Inosine fulfills the first law of thermodynamics which states that energy or matter is neither lost or gained in a chemical reaction but changes states through phases Inosine two critical roles (IMP to ATP synthesis) plus responsible for the entire degradation and recycling process qualifies it to be uracil's nucleotide partner and the sixth and final nucleotide code Inosine, itself, is the major "recycler" of "spent" amino acids (bases, sugars, phosphodiesters) IMP is the initiator of the nine step process which results in the synthesis of ATP (Adeno-Tri-Phosphate) Inosine through its IMP (Inosine Mono-Phosphate) compound is the first purine to be completed we submit Inosine replaces adenosine when a new stem, branch or shape is requiredironically dr. ferry won a nobel prize in 1953 for his discovery of the wobble position in the tRNA amino acid assembly process Inosine takes the place of adenosine when the amino acid chain begins a non-linear "cloverleaf" directional change in the third anti-codon or z (height) position, Inosine bonds with uracil, guanosine and cytosine The substitution of U for T keeps the same number of genetic nucleotide codes (i.e.) equal when DNA combines with RNA to form one of the twenty amino acids found in every protein The net difference in the substitution of U for T is the loss of 2 hydrogen protons and the gain of one oxygen proton The second major difference between d (deoxy-ribonucleic acid) DNA and r(ribonucleic acid) RNA is RNA has one more furanose pentagonal ribose sugar molecule The net difference is H3-H1 = H2 or 2 hydrogen protons (H+) Thymine has a CH3 on position 6 of the C4N2 guanosine base while uracil has only a CH1 Inosine never bonds with thymine Prescription medications are the fourth leading cause of death in the United States 300% more people die from medicines prescribed by their physician than in automobile and motorcycle accidents The current 4 dna nucleotide genetic codes are :1. (Adenosine=A), 2. (Thymine=T), 3. (Guanosine=G) and 4. (Cytosine=C) The current 4 rna nucleotide genetic codes are :1. (Adenosine=A), 2. (Uracil = U), 3. (Guanosine=G) and 4. (Cytosine=C) Uracil substitutes for Thymine in the current 4 code dna/rna amino acid synthesis process The DNA molecule resides in the nucleus of most if not all cell types The RNA molecule resides and performs its functions outside the nucleus but within the cellular walls the future of medicine is based on the foundation of the double helix model discovered in 1953 by waston and crick all current genomic technologies are based on a four (4) code genetic primer (dna = ATGC), (rna=AUGC)
ATGC = dna , AUGC = rna; AGC remain the same symbols in the same positions in the current dna/rna transcription, translation and Transformation processes The key differences between uracil and thymine are two fold: the substitution of u for t keeps the same number of genetic nucleotide codes (i.e.4) equal when dna combines with rna to form one of the twenty amino acids found in every protein the net difference in the substitution of u for t is a. the loss of 2 hydrogen protons and b. the gain of one ribose sugar molecule the second major difference between d (deoxy-ribonucleic acid) dna and r(ribonucleic acid) rna is obviously rna has one more furanose pentagonal ribose sugar molecule or one more "dose" of energy thymine has a CH3 on position 6 of the C4N2 guanosine base while uracil has only a CH1 - the net difference is H3-H1 = H2 or 2 hydrogen protons (H+) In 1966 the "almost" universal code was finally "solved" to the satisfaction of the international life sciences scientific community the "almost " universal genetic code contains 64 unique 3 bit nucleotide codes each of the twenty amino acid is composed of 3 nucleotide codes there are 4 total nucleotide codes; only 3 are used to "code" for one of the twenty amino acids since 2 is not equal to 3 then symmetry, equilbrium or charge neutrality does not exist for every two (2) A-T pairs, there are three (3) (G-C) pairsthe guanosine - cytosine pairing occurrs 50% more frequently than the adenosine-thymine pairing in rna adenosine is always covalently paired with uracil (remember u substitutes for t in dna to rna) and guanosine remains paired with cytosine Per Chargraff dna bond pairing in dna adenosine always is bonded to thymine and guanosine is bonded to cytosine Adenosine, Uracil, Guanosine, Cytosine every polypeptide is connected by the sulfur amino acid cysteine through its disulfide bonds Alternative interpretation of the scientific facts scientist discover five different nucleotides (Adenosine, Thymine, Guanosine, Cytosine and Uracil The number 5 position or structure took the place of the number 2 position or structure There are 5 known nucleotides at this point in scientific time (A,T,G,C,U) the number 2 (thymine) and number 5 (uracil) molecular structures are not the same, they are not equivalent they are not interchangeable parts remember in this substitution of U for T, 2 hydrogen protons (H2+) are lost and one ribose sugar is gained The decision was made to substitute the fifth (5) =( Uracil = U) nucleotide for the second nucleotide (Thymine = T) These 5 nucleotides represent 5 different positions in the 230 space crystalline lattice structure These 5 nucleotides represent 5 different crystalline molecular structures thymine is in reality a sulfur thioester (thiamine) which mutated to its final state by an ultraviolet light b (nm < 200nm)mutation which created an aptamer or two thymine Mathematical Operators Inosine is the best and most likely candidate for the uracil's bonding partner and sixth nucleotidein the wobble rules uracil's partner would have to be able to interact effectively with the two other pairs of nucleotides (A-T,G-C) IMP is the starter to ATP; it provides the same function as a "starter" in a
Car once the engine "starts" the starter or IMP role becomes less critical and is observed less frequently in intermediate metabolic processes ATP is produced by oxidative phosphorylation in the Mitochondria, the power generating plant organelle, in all plants and animals would have to provide mission surival critical functionality ATP is the universal energy molecule for all carbon based life forms the genetic primer's 3 codon pairs specify the x (breadth), y(length) and z (height) of the amino acid, polypeptide protein to be made the main purpose of the genetic primer is to specify the generic type of stem cell for exact shape and size and the exact atomic and molecular compound compositions the site on which the amino acid will be assembled by the ribosome would be the third purine in joining adenosine and guanosine in the last codon position (x,y,z) in the z position of the current watson crick bonding arrangements A-U is the covalent pairing would have to be able to bond to cytosine and uracil but not thymine tRNA the last of the three phases, insures the transfer and validity of the codon and anticodon strands to be assembled in the ribosomes ribosomal rna which is the actual physical interface of the biochemical molecules (nucleotides) to the crystalline molecular substrate or base of the amino acid assembly messenger rna which decodes the dna instruction set, specifies the exact sequence of codons when the double helix hydrogen bonds which bond the nucleotides together (A-T, G,C, I,U) is hydrolyzed would have to provide a non-linear solution to amino acid sequence growth and thus "budding" uracil's missing partner would have to have these characteristics or properties Inosine and the "wobble effect" or wobble rules" were formulated by Dr. Francis Crick, of double helix fame what criteria might be used to determine the identity of uracil partner and sixth nucleotide before the substitution of U for T there were five total genetic codes (A,T,G,C,U) the third pairing would be uracil and ? the sixth and final nucleotide what advantage would a 6 code genetic primer have over a 4 code genetic primer what would be the result of such a change in the current 4 code genetic primer uracil's partner would have to be involved in the major metabolic processes and amino acid synthesis uracil's partner would have to provide essential, survival level functions and services since this is not how human life or any organic life increases the number in the species in order to IMProve the chances of continued existence then it is fallacious to expect nature to use substitution and not addition in the dna to rna transformation in sexual reproduction addition not substitution is the mathematical process at work addition is nature's and therefore "the creators" algorithm for organic life, growth and evolution why would addition be more likely than substitution in the dna rna transformation what if addition were used instead of substitution as the primary dna to rna
transformation when uracil was found, what if science had found a partner for uracil instead of substituting uracil for thymine if a partner were found for uracil that would make 6 and not 4 genetic codes uracil's partner would certainly have to be found in amino acids and proteins which are "downstream" from the nucleotide phase the second pairing would be guanosine and cytosine (G-C) the first pairing would be adenosine and thymine (A-T) Addition is more predictable than substitution the purpose of the genetic code is to conserve and "pass down" successful protein building plans which will increase the odds of survival and reproduction the genetic code is a "blueprint" or master plan for constructing three dimensional proteins the final product of the nucleotide/dna/rna/amino acid synthesis process is the construction of proteins and enzymes addition would provide greater reliability and fidelity in conserving the optimized protein building specifics such as location, composition and function the use of substitution as the most reliable way to conserve the "wisdom of the genes" as accumulated over 5 billion years of evolutionary "trial and error" learning is highly unlikely a rational and logical designer would use addition and not substitution to conserve the dna encoded survial lessons one male sperm plus one female egg combine to create one unique life form the male and female, numbered two after the "offspring" was born there were now three human beings not two if substitution was used for reproduction or genetic encoding then one of the parents would be extincted and there would remain two unique life forms: (i.e. one of the original parents and the offspring) The substitution mathematical operator (i.e. Uracil (U) for Thymine (T) is a secondary mathematical process or genetic algorithm The four fundamental, basic and most elemental math operators are 1. addition, 2. subtraction, 3. multiplication and 4. division the substitution of uracil = U for Thymine = T is the only "code" difference between the dna and rna genetic codes The substitution of uracil = U for Thymine = T is the only "code" difference between the DNA and RNA genetic codes Every single prescription drug ever made has side effects The current 4 RNA nucleotide genetic codes are :1. ((Adenosine=A), 2. (Uracil = U), 3. (Guanosine=G) and 4. (Cytosine=C) The current 4 DNA nucleotide genetic codes are :1. (Adenosine=A), 2. (Thymine=T), 3. (Guanosine=G) and 4. (Cytosine=C) The future of medicine is based on the foundation of the double helix model discovered in 1953 by Watson and crick The "almost " universal genetic code contains 64 unique 3 bit nucleotide codes called codons or 192 total nucleotide bases All current genomic technologies are based on a four (4) code genetic primer (DNA = ATGC), (RNA=AUGC) Violates Inheritance Laws Violates Inheritance Laws Purines Guanosine Monophosphate
GMP
Adenosine Monophosphate
AMP
Adenosine Triphosphate ATP is the energy molecule which powers over 96% of all
metabolic reactions Evolution Missing Purine Genetic Code ADAR ADA Xanthine Hydrolase Xanthosine Oxidase IMPDH2 IMPDH1 HPGRT
IMP
Purine Catabolic Degradation Purine Synthesis Salvage Pyrmidine Metabolism First and Last Metabolic Process Steps in DNA and RNA Metabolism are certainly critical metabolic roles Inosine Family (XMP -xanthine oxidase) is final step purine catabolic metabolism; removes toxic ammonia from central nervous system - especially glutamate - the major excitatory nuerotransmitter in human brain Inosine family (IMP) starts purine nucleotide synthesis which ultimately results in the RNA and DNA Molecules Purines Purine Nucleotide Anabolic Metabolism Conversion of IMP to AMP and GMP in Purine Anabolic Metabolism from the first closed purine ring to ATP Nucleotide Side Chains, Oxidation Initiation and Metabolic Cycle Patterns Purine biosynthesis Inosine Mono Phosphate Urea Cycle Inherited Diseases, Arginine and Inosine Wobble Codon There should be an orange purine in the genetic code especially since Inosine is parent to ATP and GTP The Wobble Codons are Key Metabolic Pathway Switches The Necessity of the IMP Purine Nucleotide Family Purine ring wobble photonic diffraction Vectors Purine Metabolism Map Color Zones and Wobble Codons Arginine Inosine Wobble Diseases and the Citric Acid Cycl Consequences omitting Parent Purine from Genetic Code Conversion of IMP to AMP and GMP, IMP Parent Nucleotide, Belongs Genetic Code First Purine Base and Closed Ring First Purine Catalytic Enzymes Inosine Fractal oxidation methyl group Genetic code nucleotides and missing purine parent Genetic code wrong omitted parent purine nucleotide base IMP begins oxidation with AMP with no Oxygens IMP building blocks purine synthesis IMP First Enzyme Parent Purine IMP first purine enzyme for purine synthesis IMP initiates urea cycle stopping amino acid synthesis IMP is clearly the parent purine and precursor of AMP and GMP
IMP Root Purine Nucleotide Molecular Structure IMPDH Inhibits RNA Synthesis Initiator IMP nucleotide synthesis initiator Inosine and side effects Inosine anticodon position 34 and metabolic pathway-switching node Inosine has standard physical properties just like the other five nucleotide
genetic codes Inosine key to decoding secrets of genetic script Inosine Metabolic Functional Space used Purine Synthesis and Ammonia Removal Inosine N34 stops amino acid and starts urea cycles removal toxic ammonia Inosine orange functional boundaries Inosine parent purine nucleotide Inosine parent purine and triple helix genetic primer Inosine Parent Purine Synthesis Inosine parent purine to adenosine and guanosine
Inosine Purine Synthesis Central Internodal Connections Inosine wobble codes and functional areas degraded in purine metabolism Inosine Wobble, Arginine, and Urea Related Diseases
Nucleotides Compose Nucleic Acid Molecules Nucleotides Purine Metabolism and Wobble Codes Nucleotides, amino acids and Inosine wobble codes Nucleotides, Genetic Code, Amino Acids and Inosine Wobble Nucleotides, Purines, Inosine and the Missing Genetic Code Omitting the Parent Purine Nucleotide Negates Evolutionary Inheritance for A and G Orange Inosine is parent to red adenosine and green guanosine Oxygen and Inosine atomic molecular self-identity Parent purine structure always remains in the derivative molecular compound Purine anabolic and catabolic cycle start, stop and metabolic pathway interchanges Purine closed ring molecular atomic donors and IMP synthesis Purine Hierarchical Relationships Inosine Parent Inosine Starter of Organic Purine Synthesis AMP and GMP are made from IMP AMP and GMP are formed from IMP the parent purine
Inosine Family Inosine and IMP

amino acids coded by Inosine from the N34 position in the peptide chain Urea Cycle Inherited Diseases, Arginine and Inosine Wobble Codon The Wobble Codons are Key Metabolic Pathway Switches The Logic of Nucleotide Molecular Inheritance Purine Nucleotide Hiearchical Root Molecular Structure Purine Ring Formation, IMP and Inheritance Omitting The Parent Purine Nucleotide Negates Evolutionary Inheritance for A and G Diseases from Missing Wobble Codon Amino Acids Arginine Serine Alanine Inosine Wobble Genetic Codes and Amino Acid Codons Current 5 Genetic Code Nucleotides Omitting Parent Purine IMP
ATP & IMP mRNA Switch TCA to Urea Cycles Purine Nucleotide Anabolic to Catabolic Cycle Switch A to I Deaminase Wobble Switch IMP Starts ATP Synthesis
Inosine Parent Purine

The Purine Hexagonal Closed Ring Molecular Structure as the Foundation of The Genetic Code IMP is Parent Nucleotide Purine Molecular Structure of ATP IMP Parent Purine Inosine Family Genes, Enzymes, Proteins, and Wobble Amino Acids DNA Hydrolysis by DNA deoxyInosine ( 3.2.2.15) glycosidase Biosynthetic End Products from Alpha Ketoglutarate and Arginine Xanthine Enzyme Multi-Function Nucleotide Compounds Xanthine Oxidase Oxidation Mechanism and Uric Acid Eliminiation Omitting The Parent Purine Nucleotide Base IMP is The Second Fatal Flaw of the Current Genetic Code Natures Ingenious 3 bit Codon even Codes for bi-lateral Symmetry (i.e. left and right hands) Using the Dominant (5) and Recessive (3) Nucleotide Complementary Pairing made Famous by Watson and Crick Each Purine-Pyrmidine Nucleotide Base Pairing (IMP-UMP, AMP-TMP, GMP-CMP) is the X (width), Y (length) or Z (height) specification for making each of the 20 Standard Protein Amino Acids Position Three is for the Z or Height Dimension and Contains three or tri-phosphate esters with three hydrogen bonds The Third Codon is Quite IMPortant Contrary to Conventional Genetic Code Wisdom The GMP-CMP Nucleotide Base Pair is the Third and Last Covalent Partnering of the Novagon DNA Triple Helix 6 Code Genetic Primer Position Two specifies the Y or length dimension and the Di-Phosphate Nucleotide The Second Genetic Code Nucleotide Base Pair is AMP Covalently Bonded to TMP with two hydrogen bonds Position One of the Codon specifies the X dimension and one mono phosphate The First Genetic Code Nucleotide Base Pair is IMP and UMP with one hydrogen bond IMP is the Evolutionary Parent Purine Nucleotide for ITP, GTP and ATP ATP had not been produced through phosphorylation before IMP began the Purine Nucleotide Synthesis de novo Process ATP is The Universal Energy Molecular Structure which Powers 96% of all Metabolic Cycles Inosine Mono Phosphate (IMP) - Was Natures First Purine Nucleotide Molecular Structure Inosine Enzyme Nucleotide Compounds Inosine Thermodynamic Parameters for Binding Drugs to DNA Inosine Metal Binding and Ligand Stability Constants IMP & XMP Metal Binding Cofactors Purine Nucleotide Family Inheritance Tree Conversion of IMP to AMP and GMP is a Classic Parent Child Inheritance Relationship IMP parent purine base nucleotide of ATP & GTP Interconversion Purine Nucleotides by IMP Catalytic Starter ATP Synthesis The IMP Purine Parent with his XMP Partner
Purine Nulceotide Catabolic Metabolism Metabolism of Ammonia Eliminating Toxic Ammonia is a Survival Level Functions and Representation in the Genetic Code Purine Catabolic Degradation and Recycling Purine Catabolic Metabolism and Uric Acid Toxic Ammonia Elimination Purine Salvage and IMP Parent Purine Nucleotide Omitted in the Current Genetic Code Urea Cycle, Toxic Ammonia Removal and Xanthine Oxidase Enzyme Inosine Mono Phosphate Urea Cycle Inherited Diseases, Arginine and Inosine Wobble Codon There should be an orange purine in the genetic code especially since Inosine is parent to ATP and GTP The Wobble Codons are Key Metabolic Pathway Switches The Necessity of the IMP Purine Nucleotide Family Purine ring wobble photonic diffraction Vectors Purine Metabolism Map Color Zones and Wobble Codons Arginine Inosine Wobble Diseases and the Citric Acid Cycl Consequences omitting Parent Purine from Genetic Code Conversion of IMP to AMP and GMP, IMP Parent Nucleotide, Belongs Genetic Code First Purine Base and Closed Ring First Purine Catalytic Enzymes Inosine Fractal oxidation methyl group Genetic code nucleotides and missing purine parent Genetic code wrong omitted parent purine nucleotide base IMP building blocks purine synthesis IMP First Enzyme Parent Purine IMP first purine enzyme for purine synthesis IMP initiates urea cycle stopping amino acid synthesis IMP is clearly the parent purine and precursor of AMP and GMP IMP Root Purine Nucleotide Molecular Structure IMPDH Inhibits RNA Synthesis Inosine and side effects Inosine anticodon position 34 and metabolic pathway-switching node Inosine has standard physical properties just like the other five nucleotide genetic codes Inosine key to decoding secrets of genetic script Inosine Metabolic Functional Space used Purine Synthesis and Ammonia Removal Inosine N34 stops amino acid and starts urea cycles removal toxic ammonia Inosine orange functional boundaries Inosine parent purine nucleotide Inosine parent purine and triple helix genetic primer Inosine Parent Purine Synthesis Inosine parent purine to adenosine and guanosine Inosine Purine Synthesis Central Internodal Connections Inosine Starter of Organic Purine Synthesis Inosine wobble codes and functional areas degraded in purine metabolism Inosine Wobble, Arginine, and Urea Related Diseases Purine Hierarchical Relationships Inosine Parent
Purine closed ring molecular atomic donors and IMP synthesis Purine anabolic and catabolic cycle start, stop and metabolic pathway interchanges Nucleotides Compose Nucleic Acid Molecules Parent purine structure always remains in the derivative molecular compound Orange Inosine is parent to red adenosine and green guanosine Omitting the Parent Purine Nucleotide Negates Evolutionary Inheritance for A and G Nucleotides, Purines, Inosine and the Missing Genetic Code Nucleotides, Genetic Code, Amino Acids and Inosine Wobble Nucleotides, amino acids and Inosine wobble codes Nucleotides Purine Metabolism and Wobble Codes Oxygen and Inosine atomic molecular self-identity Initiator IMP nucleotide synthesis initiator AMP and GMP are made from IMP IMP begins oxidation with AMP with no Oxygens AMP and GMP are formed from IMP the parent purine Purine Nucleotide Anabolic Metabolism Conversion of IMP to AMP and GMP in Purine Anabolic Metabolism from the first closed purine ring to ATP Nucleotide Side Chains, Oxidation Initiation and Metabolic Cycle Patterns Purine biosynthesis Purine Nulceotide Catabolic Metabolism Metabolism of Ammonia Eliminating Toxic Ammonia is a Survival Level Functions and Representation in the Genetic Code Purine Catabolic Degradation and Recycling Purine Catabolic Metabolism and Uric Acid Toxic Ammonia Elimination Purine Salvage and IMP Parent Purine Nucleotide Omitted in the Current Genetic Code Urea Cycle, Toxic Ammonia Removal and Xanthine Oxidase Enzyme 5-phosphoribosylamine Closed Ring Purine Synthesis de novo IMP The First Purine Nucleotide "closed" ring Molecular Structure First Purine Nucleotide Closed Ring Structure and Purine Nucleotide Synthesis First Closed Purine Nucleotide Ring IMP The First Closed Purine Nucleotide Molecule Paved The Way for DNA and RNA to Evolve IMP The First Purine Nucleotide "closed" ring Molecular Structure First Purine Nucleotide Closed Ring Structure and Purine Nucleotide Synthesis First Closed Purine Nucleotide Ring IMP The First Closed Purine Nucleotide Molecule Paved The Way for DNA and RNA to Evolve Purine Nucleotide Family Inheritance Tree Conversion of IMP to AMP and GMP is a Classic Parent Child Inheritance Relationship IMP parent purine base nucleotide of ATP & GTP Interconversion Purine Nucleotides by IMP Catalytic Starter ATP Synthesis The IMP Purine Parent with his XMP Partner
Inosine Mono Phosphate

Urea Cycle Inherited Diseases, Arginine and Inosine Wobble Codon There should be an orange purine in the genetic code especially since Inosine is
parent to ATP and GTP The Wobble Codons are Key Metabolic Pathway Switches The Necessity of the IMP Purine Nucleotide Family Purine Metabolism Map Color Zones and Wobble Codons Purine ring wobble photonic diffraction Vectors Purine Hierarchical Relationships Inosine Parent Purine closed ring molecular atomic donors and IMP synthesis Purine anabolic and catabolic cycle start, stop and metabolic pathway interchanges Parent purine structure always remains in the derivative molecular compound Oxygen and Inosine atomic molecular self-identity Orange Inosine is parent to red adenosine and green guanosine Omitting the Parent Purine Nucleotide Negates Evolutionary Inheritance for A and G AMP and GMP are made from IMP Arginine Inosine Wobble Diseases and the Citric Acid Cycl Consequences omitting Parent Purine from Genetic Code Conversion of IMP to AMP and GMP, IMP Parent Nucleotide, Belongs Genetic Code First Purine Base and Closed Ring First Purine Catalytic Enzymes Inosine Fractal oxidation methyl group Genetic code nucleotides and missing purine parent Genetic code wrong omitted parent purine nucleotide base IMP begins oxidation with AMP with no Oxygens IMP building blocks purine synthesis IMP First Enzyme Parent Purine IMP first purine enzyme for purine synthesis IMP initiates urea cycle stopping amino acid synthesis IMP is clearly the parent purine and precursor of AMP and GMP IMP Root Purine Nucleotide Molecular Structure IMPDH Inhibits RNA Synthesis Initiator IMP nucleotide synthesis initiator Inosine and side effects Inosine anticodon position 34 and metabolic pathway-switching node Inosine has standard physical properties just like the other five nucleotide genetic codes Inosine key to decoding secrets of genetic script Inosine Metabolic Functional Space used Purine Synthesis and Ammonia Removal Inosine N34 stops amino acid and starts urea cycles removal toxic ammonia Inosine orange functional boundaries Inosine parent purine nucleotide Inosine parent purine and triple helix genetic primer Inosine Parent Purine Synthesis Inosine parent purine to adenosine and guanosine
Inosine Purine Synthesis Central Internodal Connections Inosine Starter of Organic Purine Synthesis Nucleotides, Purines, Inosine and the Missing Genetic Code Inosine wobble codes and functional areas degraded in purine metabolism Inosine Wobble, Arginine, and Urea Related Diseases
Nucleotides Compose Nucleic Acid Molecules Nucleotides Purine Metabolism and Wobble Codes Nucleotides, amino acids and Inosine wobble codes Nucleotides, Genetic Code, Amino Acids and Inosine Wobble AMP and GMP are formed from IMP the parent purine
Inosine Family Genes, Enzymes, Proteins, and Wobble Amino Acids Inosine Enzyme Nucleotide Compounds Inosine Thermodynamic Parameters for Binding Drugs to DNA Inosine Metal Binding and Ligand Stability Constants IMP & XMP Metal Binding Cofactors DNA Hydrolysis by DNA deoxyInosine ( 3.2.2.15) glycosidase
Biosynthetic End Products from Alpha Ketoglutarate and Arginine Xanthine Enzyme Multi-Function Nucleotide Compounds Xanthine Oxidase Oxidation Mechanism and Uric Acid Eliminiation Omitting The Parent Purine Nucleotide Base IMP is The Second Fatal Flaw of the Current Genetic Code IMP is the Evolutionary Parent Purine Nucleotide for ITP, GTP and ATP ATP did not Exist before IMP began the Purine Nucleotide Synthesis Process ATP is The Universal Energy Molecular Structure which Powers 96% of all Metabolic Cycles Inosine Mono Phosphate (IMP) - Was Natures First Purine Nucleotide Molecular Structure Each Purine-Pyrmidine Nucleotide Base Pairing (IMP-UMP, AMP-TMP, GMP-CMP) is the X (width), Y (length) or Z (height) specification for making each of the 20 Standard Protein Amino Acids Position Three is for the Z or Height Dimension and Contains three or tri-phosphate esters with three hydrogen bonds The Third Codon is Quite IMPortant Contrary to Conventional Genetic Code Wisdom The GMP-CMP Nucleotide Base Pair is the Third and Last Covalent Partnering of the Novagon DNA Triple Helix 6 Code Genetic Primer Position Two specifies the Y or length dimension and the Di-Phosphate Nucleotide The Second Genetic Code Nucleotide Base Pair is AMP Covalently Bonded to TMP with two hydrogen bonds Position One of the Codon specifies the X dimension and one mono phosphate The First Genetic Code Nucleotide Base Pair is IMP and UMP with one hydrogen bond Natures Ingenious 3 bit Codon even Codes for bi-lateral Symmetry (i.e. left and right hands) Using the Dominant (5) and Recessive (3) Nucleotide Complementary Pairing made Famous by Watson and Crick Pyrmidines Pyrmidine Nucleotides Pyrmidine Nucleotide Anabolic Metabolism Pyrmidine Nucleotide Catabolic Metabolism Interconversions and Degradation of Pyrmidine Nucleotides and XMP Ribonucleases Pyrmidine Metabolism, Thioredoxin Reduction and Nucleic Acid Polymerases Genetic Code Violates Inheritance Laws - Omits Parent Purine Nucleotide Inosine Monophosphate (IMP) - Purine Synthesis De Novo " from scratch" Purine and Pyrmidine "de novo" Metabolism Synthesized The First Evolutionary Nucleic Acids (RNA & DNA) "Closed Ring" allowed Photosynthetic Photons (electrons & protons) to be
captured by closed crystalline molecular structure IMP - First " Closed Purine Ring" Nucleotide made by Nature Purine Synthesis "de novo" -Most complex molecular structure synthesis in nature - 14 dufferent enzymatic intermediate structures involved Omits Parent Purine Nucleotide - Inosine Monophosphate (IMP) IMP Begins Purine Synthesis De Novo Purine Nucleotide Synthesis De Novo Makes Molecular Structures for DNA and RNA Molecules AMP and GMP are Formed From IMP Nucleotides Thioester Phosphates Pentose Sugars Nitrogen Bases Structures of Nucleotides and Nucleosides ATP is the energy currency of metabolic reactions in cellular operations by cellular organelles i.e. mitochdondria, ribosomes Structures of Nucleotides and Nucleosides Scientist discovered five different nucleotides (Adenosine, Thymine, Guanosine, Cytosine and Uracil) Remember in this substitution of U for T, 2 hydrogen protons (H2+) are lost and one oxygen is gained The number 2 (thymine) and number 5 (uracil) molecular structures are not the same, they are not equivalent they are not interchangeable parts The number 5 position or structure took the place of the number 2 position or structure The decision was made to substitute the fifth (5) =( Uracil = U) nucleotide for the second nucleotide (Thymine = T) These 5 nucleotides represent 5 different positions in the 230 space crystalline lattice structure These 5 nucleotides represent 5 different crystalline molecular structures Nucleotides
Adenosine Guanosine Inosine

Xanthosine Purine Nucleosides are composed of four major molecular structures Inosine Purine Parent Purine Bases Pyrmidine Bases Nucleosides are made up of nitrogen bases Purine Nucleosides Pyrmidine Nucleosides Nucleotides are made up of nucleosides Purine Nucleotide Bases
IMP
AMP GMP
IMP Family
The entire concept of inheritance and evolution rests on "new generations" (i.e. GMP and AMP) of molecules starting with " a template" or organic molecular structure; since Inosine was the first purine to possess the critical "closed
ring" molecular structure and GMP and AMP are derived from IMP why wouldn't the first purine molecule be the first purine genetic code IMP (E.C. = 1.1.1.1.250 is the lowest purine enzyme classification number which means it came before all other purine enzymes; Besides being the first enzyme, the first purine closed ring Inosine also has the perfect molecular structure to start an oxidation-reduction biochemical reaction between two chemical species i.e. Adenosine has no oxygen but only a NH2 (ammonium side radical) ATP would never have evolved into it's present state and critical molecular function if the parent IMP did not develop the closed purine ring Omitting Inosine from the genetic code means either Adenosine or Guanosine is taking its legitimate place in the linear sequence of amino acids/codons; When A replaces I then the covalent pair lose their ability to be oxidized at a lower temperature or energy state; this makes the cell take valuable energy from other critical redox enzyme proteonic reactions If Guanosine is substituted into a specific atomic amino acid cell site then the molecule gets the O2 molecule for oxidation but also adds an NH2 or ammonium ion which causes an imbalance in the ammonia/urea cycle elemination process which is crucial for cellular heath; besides oxidation, ammonia is the dangerous threat to the brain master control center One has to assume in over 3.6 billion years that each nucleotide base code has only one amino acid associated with it; the genetic code is not degenerate; it is man's inability to use the more specific genetic information encoded in the atomic genetic primer which is atom specific; ie. there are 230 possible node or connecting points in the various three dimensional crystalline lattice structures which make up the "frame " of the gene; since 1 helical spiral has 10 turns between purine base pairs then 230/10 = 23 chromosomes DNA is half protein (histones) and half dna ; it should be possible to "map" the exact location of the twenty three chromsomes over the three dimensional space the crystalline structure extends; we have calculated the maxium number of base pairs that each of six nodes can have for the purine/pyrmidine nucleotides If A and G, the children of I (IMP = GMP, AMP two different pathways); if the 2 children are in the genetic code then their common parent, Inosine or IMP must also be in the genetic code primer Inosine is precursor IMP nucleotide to GMP and AMP or GTP and ATP ; two most IMPortant energy sources for internal (GMP = dna /rna transcription and translation processes); ATP external or extrons to invidivual cell; is a network charger = ATP These are the "wobble" nucleotide base pairings Inosine forms (I) - (U,C,A) and the three metabolic wobble "switched" anabolic and catabolic pathways Purine Catabolic, Decomposition and Recycling Cycle (salvaging "left over" purine bases, ribose sugar, and phosphodiester organic atoms for beginning IMP to ATP 9 step anabolic reaction Inosine and the wobble position - anti-codon branching point for beginning of catabolic purine process AMP + asparate = Inosine = IUG ; stop protein synthesis; begin recycling and new set up for different amino acid; Inosine can bond with Cystosine (first choice), Uracil (second choice) and take the place of Adenosine (adenosine deaminase = mRNA editing) - violation wobble tRNA rule and central dogma linear model; numerous instances where both positive and
negative feedback processes regulate macromolecular anabolic and catabolic reactions Inosine only purine base to be able to bond to three different partners; maximum flexibility and IMProves purine pathways from 2 to 3; allows for feedback sytems to develop; one needs three objects or processes to make a comparison and adjustment This is a metabolic map of purine metabolism showing the criticality of Inosine, IMP, Xanthine, Hypoxanthine and all the "orange" metabolic nodes
Inosine Mono Phosphate - first purine "closed ring" hexagonal heterocyclic

benzymatic molecular structure; fundamental nucleotide of genetic code protein primer IMP is the precursor purine parent to ATP and GTP IMP is first totally closed purine base ring Inosine Mono Phosphate Parent Purine IMP, precursor biochemical parent of AMP and GMP has the Perfect Molecular Structure and Optimal Number and Type of Purine Ring Side Atomic Molecular Structures There are two major metabolic cycles IMP or Inosine, hypoxanthine (base), xanthine (base), Inosine (nucleoside), Inosine monophosphate (nucleotide) IMP is made from: 1. three amino acids (glycine, aspartate, and gluamine), 2. a tetrahydrofolate cofactor (10 Formyl Tetrahydrofolate), 3. a Carbon Dioxide (CO2), 4. PRPP (Phosphoribophosphate) - ribose sugar) with the IMPDH (inosinic acid -dehydrogenase enzyme E.C. = 1.1.1.1.250) IMP has only "one" oxygen on its side chain; AMP has no Oxygen Atoms in the Adenosine base Molecular Structure; since it has no oxygen's a self-bonding of A-A has two NH2 side chains but no Oxgen; it has to wait for the pentose/ribose nucleoside sugar to connect to the adenosine base before it can become metabolically active If the Two Purine Nucleotide Molecular Strutures of the "Children" of Inosine Mono Phosphate (1.1.1.1.250) are in the Present Genetic Code Then the Parent Purine Nucleotide Molecular Structure must also be in that Same Genetic Code IMP is the first purine nucleotide to have a "closed ring structure" IMP is formed in a nine step synthesis from the following 6 different atomic molecular donors Glutamine, Glycine, Aspartate, N10 Formyltetrahydrofolate, CO2, PRPP IMP, IDP, ITP IMP begins purine metabolism which terminates with the production of the triphosphates i.e. ATP, GTP, ITP AMP Family AMP-S, AMP, ADP, ATP, ATP and GTP along with ITP are the purine nucleotides of the Genetic Primer GMP Family Purine Anabolic, Growth and Synthesis Cycle Purine Nucleotide Synthesis XMP, GMP, GDP,GTP Urea Cycle Arginine Purine Nucleotides are composed of three major molecular structures with 3 or 4 isotopic alleles These are the 12 nucleosides (6) and nucleotides (6) which make up the genetic
codes which specify and coordinate protein synthesis Purine Anabolic and Catabolic Biomolecular Metabolic Redox Reactions Methyl- Inosine Thio-Inosine Hypoxanthine Xanthine Oxidase Inosine and IMP = Hydrogenase = 1.1.1.1.250 Glutamine Glycine Aspartate 1 N10 Formyl Tetrahydrofolate 1 CO2 Aspartate 2 N10 Formyl Tetrahydrofolate 2 PRPP Purine Nucleotide Closed Ring
IMP
XMP GMP GDP GTP AMP-S AMP ADP ATP DNA Nucleic Acid ATPase Water Ammonia AMP
IMP
XMP Xanthine Oxidase Uric Acid Urate Ammonia Eliminated GMP RNA Nucleic Acid RNA Genetic Code A2 - U1 G2- C2 ATP Nucleotide UTP Nucleotide Adenosine Base Uracil Base DNA Genetic Code A1 - T1 G1- C1
ATP Nucleotide TTP Nucleotide
Adenosine Base Thymine Base

A purine nucleotide with no side groups but hydrogens has 9 different and unique bonding positions; even though a 6 and 5 sided (hexagon + pentagon) are fused together, they share a common carbon bond thus substracting 2 sides, thus 11 -2 = 9 thus in the purine electrochemical circuit their are nine different potential oxidation states each corresponding to sulfur's (+6,+5,+4,+3,+2,+1,0,-1,-2 ); it is interesting to note that the maximum positively c
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Detailed Summary (berger overview.txt)
We will demonstrate, beyond a shadow of a doubt, that inosine-and all it s extended progeny (hydroxanthine, xanthine, inosine, IMP, IDP, ITP etc.) should join adenine-and guanine-in increasing the number of nucleotide purine bases from two to three. There are currently three Pyrmidine bases -thymine,-cytosine, and-uracil). We have very strong reason to believe that nature intended the purines and pyrmidines to be balanced and for the genetic code to have three sets of purine-pyrmidine covalent base pairings ( adenine-thymine, guanine-cytosine, inosine-uracil)... First, inosine is the parent purine.to adenine and guanine. Inosine is the first linearized chain of amino acids.to form a closed ring i.e. purine. Without inosine there would be no organic aromatic heterocyclic compounds. There would be just long chains of amino acids... So the fact inosine is the first purine is a very, very, very, big deal. Without the parent there can be no children. Without inosine there would be no adenine or guanine. If there were no adenine, there would be no ATP (adeno-triphosphate), the energy molecule of all cells in all carbon based life forms. Without ATP to power photosynthesis, glycolysis and all other major metabolic pathway reactions, there would be no life on earth... Let s take a big picture view of the major purine, pyrimidine, nucleoside, nucleotide, dna, rna, amino acid, protein and enzyme metabolic pathways and feedback systems. For simplicity sake, we have color coded the purines and pyrmidines so that can be easily distinguished... The coloring scheme is as follows: adenine is red, inosine is orange, guanine is green, thymine is yellow, cytosine is blue, and uracil is purple... Imagine while viewing figure 1 that the dna and rna processes are railroad yards where linear amino acids are coupled, decoupled, reassembled, and transported by way of non-linear switches. Looking at the figure, Observe the color coded purines and pyrmidines. Observe how these colored.. Logic dictates that if the children purines of adenine and guanine are part of the genetic code, then their parent inosine should also be included in that very same code. Without a starter a car or any machine is not very useful. If you have no inosine molecules to create purine rings then both transcription and translation coding errors will occur... It has been ably demonstrated that point mutations or base pairings with one code substitutions can cause major genetic diseases such as:.. NAME OF GENETIC Diseases from point mutations or substitutions... This leads us to our third argument, that addition and not substitution is nature s genetic growth algorithm... From over thirty two years of research I have never seen a good reason or for that matter any reason given why uracil should substitute for thymine in the dna to rna transcription and
file:///C:/Users/dr%20john%20allen%20berger/Des...9681172124817327570183.berger_overview.txt.htm (1 of 2) [4/27/2008 12:21:19 AM]
Detailed Summary (berger overview.txt)
transformation processes. Why does U take the place of T in the current 4 code genetic primer? They are not the same molecular compound. They are not equivalent. In fact, two hydrogen protons H2+ are lost when uracil takes the place of uracil since thymine has a CH3 while uracil has a CH1 on the six position purine cyclic base... If U does in fact take T s place in nature s 2.8 billion year old genetic primer then we should not expect to find both thymine and uracil in any dna, rna, amino acid or protein residues. If U substitutes for T then T is substracted from the set or pool of pyrmidine bases in constructing the polypeptides in the cytoplasmic ribosomes. The fact is that when genetic (dna and rna ) sequencing is performed one does find both thymine and uracil in the same residues. That means thymine was not substituted for or deleted from the pyrmidine resource pool. Both Uracil and Thymine belong in the final genetic code just as inosine belongs... When all is said and done we strongly believe that the genetic code should have 6 not 4 nucleotide codes. Instead of substituting U for T, we at Novagon DNA have added inosine and paired it with uracil. So in point of fact, nature s true genetic primer has adenine paired with thymine, guanine paired with cytosine, and inosine paired with uracil... Finally, by observing how nature and evolution have created the millions of different species it is apparent that addition and not substitution is the mathematical operator at work. If nature used substitution instead of addition for sexual reproduction then the child would take the place of one of the parents and the species s number would never increase. One can only grow and expand through addition and multiplication, not substitution or subtraction... It is further apparent that the human genome has grown by way of addition and not substitution. Only through symbiosis and cooperation can the whole organism enlarge it s repertoire of functionality. The old adage that 1 plus 1 equals 3 or the whole is greater than the sum of its parts has never been truer for this instance. Biological mathematics is not the same as inorganic mathematics and that difference should be studied in more detail...
file:///C:/Users/dr%20john%20allen%20berger/Des...9681172124817327570183.berger_overview.txt.htm (2 of 2) [4/27/2008 12:21:19 AM]
Detailed Summary (My name is Dr John Allen Berger.txt)
I am prepared to demonstrate quite conclusively that the current Watson-Crick double helix 4 code genetic primer is incorrect, and in fact should be a 6 code genetic primer and not a 4 code primer. It is the different between a password with 4 digits.and a password with 6 digits. The current dna 4 code primer uses the wrong mathematical operator in transforming dna to rna. There is a reason every medicine and every organic molecule made by modern science has side effects often fatal... 2. The Second domain in addition to the double vs. triple helix validation proof, is the discovery,of the first contributor to the planet earth genome, the first life form (i.e. purple bacteria) to donate and contribute it's rna molecular formulation to what has now become the human genome. This bacterium leads to the third great discovery, of which the first rna donor is a subcategory or organic manifestation of the 6th and final organic atomic element... 3. This 6th atomic element is older than earth. as will be shown it is the super chemical connnector and linker of life on earth. It is the "supervisor" of the other atomic elements which compose the atomic element periodic chart... My "Science of Evolution" for want of a better title traces the path of this 6th organic atomic element joining (hydrogen1, carbon12, nitrogen14, oxygen16 and phosphorous31. The current double helix has not recognized the importance of this element because the scope and different coloring identities this element assumes, literally starting, stopping and directing the other atomic elements to their specific destinations (i.e. building proteins and specifically enzymes) according to crystalline molecular structural blueprint instructions for every e=mc3 reaction on earth... These 3 scientific but integrated results, if true, and I am prepared to present a very comprehensive powerpoint presentation (actually multiple story boards) which is color coded and literally a concept map of biomolecular chemistry and the protein, fatty acid and polysaccyhride metabolic processes...
file:///C:/Users/dr%20john%20allen%20berger/Deskto...380736010.My_name_is_Dr_John_Allen_Berger.txt.htm [4/27/2008 12:22:46 AM]
Detailed Summary (Berger beginning2.txt)
Detailed Summary Print this page

FILEPATH M:\berger writings\txt berger\Berger beginning2.txt
? Critical to the entire thread of evidence is the number 6 and the letters "S" and "TH". You will see as we take our journey from the atmosphere of Venus to the Jupiter moon, Ito. They both contain sulphur as does every important organic and inorganic compound known to man. We will show how each of the ? Periodic chart atomic elements play a key role in the healthy and fully functional species, called HomoSapiens. However, man has vastly underestimated the power of sulphur and this carelessness has and will create more viral and cancerous conditions... ? This paper we'll demonstrate beyond a shadow of a doubt that the current DNA and RNA codes are incorrect and offer a new six alpha code organic primer to replace the current for digit the DNA codes. We will show that sulphur with its 22 isotopes from s 49 to s 27 is the master atomic element and controls all inorganic and organic chemical processes. We really demonstrate this by showing the vast array critical organic and inorganic compounds and reactions which sulphur controls in its many many guesses. Our evidence comes from each level of molecular to growth from the atomic elements to the Thalmus of the human midbrain... ? Sulphur and sulfur and different compounds and need to be defined... ? Hydrogen (H), Carbon (C), Nitrogen (N) , Oxygen (O), Phosphorous (P) and Sulfur (S),... ? The current dna and rna codes only uses the first five atomic elements (H,C,N,O,P), the thrust of this paper attempts to demonstrate why Sulfur (SF) & Sulphur (SPH) belong in this select core group of basic atomic building blocks. We distinguish between Sulfur (SF) & Sulphur (SPH) on the of the two different organic processes the SF and SPH composites control. SF regulates the ? Thiol relationships, while SPH controls the more normal Phosphorylation interactions... ? Why should SF and SPH be included in this select subset of atomic elements? We strongly believe the hardiest life form s (green bacteria, cyanobacteria, live in volcanic boiling water sulfur springs (temperature > 212 degrees farenheigt )dna belongs in the evolutionary based human genome, These green bacteria were the only "life forms" on earth for at least 10 million years, until the earth cooled enough for other life forms to survive. We believe the original dna code belongs to this class of thermophilic uni-cellular organic entitites. Not surprisingly, these green bacteria are sulfur composite entities. Logically, the hardiest life form who is still living today deserves to be represented in the human genome, somewhere. Speculating we believe one of the "ice ages" caused one of the sides of the crystal lattice structure "arms" or "legs" broke off and this became the second living entity... ? Nonetheless, the oldest living life form has to be represented some where in the human
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genome and the fact this hardiest of life forms is sulfur composed adds to the empirical and logical evidence we are accumulating for our comprehensive proof... ? Table 1 demonstrates that in Sanger reactions. sulfur can assume all six primary colors when interacting with the five other atomic elements (H,C,N,O,P). In fact we will make the case that ? These five elements are "the children of sulfur" as one of the 10 non-radioactive, stable isotopes ? Sulfur can exist as. Remember, isotopes are not identical twins or clones, but separate entities with ? Distinctly different properties, functions and reactions... ? Sulphur along with carbon predates human history. Because of its association with volcanic eruptions, hot molten smelly lava, and extremely acidic nature, has been associated with evil, as evidenced by the religious idiom, "Fire and brimstone . The brimstone refers to sulfur... ? On earth, in inorganic and organicmetallic reactions sulfur is again the major player. The disulfide ? Bond is the bridge which not only holds the dna intranuclear bonds together but also provides the ? Essential salts necessary for organic life. (Sodium sulfate, Potassium sulfate, Lithium sulfate, ? Magnesium sulfate, etc... ? Table 3 shows all the rocks and mineral sulfur combines with. The sulfates, sulfides, and sulfosalts are the most important natural sources for the trace elements which are necessary for organic life to occur. Would it surprise you that the hemoglobin, the key ingredient in our red blood cells is iron ? Sulfate. That's right, sulfur is literally at the very "heart" of the human being where oxygen, carbon dioxide, and other important gases exchange ions and plasma nutrients... ? In fact, the most fundamental flaw with "the central dogma" is that it is a totally linear model with linear Metaphors (twisted step ladders, chairs, tables, railroad tracks etc.), linear statistics and linear or square products. The four dna codes (A,T,G,C) and 4 rna codes (A,U,G, C), (uricidine substitutes for thymine in the 3 step translation, messenger, and transcriptions phases of the dna conversion to ? tRNA. Actually, the Watson Crick Celera Model contains 5 nucleotide codes (A,T,U,G,C). The mistake Watson and Crick made was to substitute U for G instead of looking for a partner for Uricidine. It would not been hard to find, if they had perceived the true meaning of the secretive ? "wobble effect" where Inosine takes the place of Adenine in a variety of Amino Acid triple helix ? lattice structures. Therefore, we are proposing adding a sixth nucleotide code = I for Inosine... ? We intend to prove beyond a shadow of a doubt that the current Double Helix DNA model articulated by Drs. James Watson and Francis Crick in 1953 and in doing so winning a Nobel prize. Their double Helix Model was never really been challenged seriously by the competing triple helix Model led by ? by Drs. Frazer of Germany and Dr. Linaus Pauling of the United States. in fact, Watson pressured the Cambridge journal science which was the leading Journal of its day to omit any articles about the triple helix. This many. Miscarriage of Justice is about to be remedied ? However, The Novagon DNA triple helix model bears little resemblance to the original model and in fact we can never obtain a copy to check it out. Novagon DNA in a
much more than a DNA primer it is an integration of all life sciences from the organic atomic elements to the giant macro molecules... ? The central figure in the Novagon model in the organic atomic element named sulfur. Sulfur is the sixth and final organic atomic element. The current DNA model uses only by atomic organic elements, hydrogen, carbon, nitrogen, oxygen and phosphorus Our model is based on the atomic mass unit, what you the standard way of measuring atomic matter, particles, and crystal lattices. hydrogen had an atomic mass unit of 1.008, carbon twelve, nitrogen fourteen, oxygen sixteen, phosphorus 31, and sulfur 32 add up to 106 ATMUs. Therefore, adding 0.30.19% more mass to the dna genome base... ? The current the DNA model is composed of 4 nucleotide,molecules named: adenine, thymine, the guanine and cytosine. The fifth and final nucleotide, uracil or uricidine is substituted for thymine when DNA is transformed into RNA which of the final genetic instructions given to the cellular organisms such as the mitochondria, ribosomes, and golgi bodies. these cellular organisms make up the amino acids and protein manufacturing workforce. The Novagon triple helix model has a patented optical chromatic messaging system which uses the heat values of the six prime colors red, Orange, yellow, green, blue and violet or purple. It is the discrete color bands which act as and organic bar coding system... ? The Novagon triple helix DNA model uses the mathematical operation of the addition rather than substitution in the DNA RNA amino acid protein production process. Instead of substituting uricidine for thymine, the triple helix model adds a six and final nucleotide called Inosine. The the double and triple helix models you different mathematical operations to transmit the DNA instruction sets to the organic workers who implement and execute the RNA genetic primer... ? This research will be reported using a new scientific type of document called scientific electronic new a news book. This book will be the foundation of our research on the sixth DNA element which we are proposing to elevate and join hydrogen, carbon, nitrogen, oxygen, and phosphorus. These are the current five atomic elements of which make up the five nuclear tides of adenine, thymine, guanine, cytosine, and uracil. In the current Watson Crick DNA double helix model, uracil is substituted for thymine which essentially substitutes a methane gas for a water molecule. The OH- radical is replaced by The NH2 complex and thus sealing the doom for the number four benzene ring position occupied by the second and last nitrogen on the 6 sided hexagon dna base of C4,N2. We have strong circumstantial evidence that ? before sulfur arrived on earth, the dna hexagonal base was C3N3, a very balanced, symmetrical shape which nature seems to prefer. The fact the human dna base has lost one amine is not good. Nitrogen represents green, plants, life, photosynthesis etc. Carbon is one step removed from ossified calcium and when that occurrs osteperososis/carboxylation occurrs and the carbon atom changes from the organic to ? the inorganic state, namely coal, soot, and other hydrocarbons... ? An explanation is in order of course. Language is a man made invention while mathematics
is not. Why is it that the first human languages from all our archaeological, anthropological, and carbon fourteen fossil dating records began from the right and written script proceeded from right to left. English, on the other hand, is written from left to right. Why is this important? Because the universal, cosmic magnetic flux river flow is counterclockwise that is, from right to left. The earth spins counterclockwise on its axis, the earth revolves counterclockwise around the sun in 366 days. Our weather patterns and jet streams ? move counterclockwise. Even opening most faucets requires counterclockwise motion. Clockwise is ? shutting off, choking, cutting off. That is was sulfur is doing to our dna codes, causing randomly generated mutations, retrograde viruses, and superstrains of bacteria which are immune to our most ? powerful strains of bacterial hybridized colonies... ? With hundreds if not thousands of pictures, schematic and diagrams, we we'll provide the most comprehensive analysis and documentation of all sulphur related organic and inorganic compounds... ? Lets us begin this tale of research as the intellectual exploration of one "different" and unique person, named DrKyia as embarked on. When DrKyia puts his scientific terms in "google", and nothing "pops up", DrKyia knows he is headed in the right direction, that is, where no other scientist has gone... ? To this point, DrKyia has read and used over 1130 Ph.D level scientific books in the past three years, from 1999-20001. He had a lot of catching up to do since he flunked organic chemistry in college and became an industrial/organizational psychologist instead. For twenty years, Dr Kyia, assessed and evaluated thousands of executives, scientists, managers, technical, sales and virtually all functional business and engineering functions ? But, in 1999 DrKyia 's life changed dramatically, and happened on the death bed of him beloved mother, who told DrKyia, that he was special and he had a very important mission which would effect mankind. DrKyia, had always known he was different, and he did indeed fill "special" but what did the cryptic message from his drug impaired mother mean? ? DrKyia continued on with his life, but that final conversation with his mother kept nagging at him. Sure, he knew he came from an extremely intelligent gene pool, evidenced by the educational, professional and life styles all his extended family members enjoyed... ? It is sulfur that is the first compound to be ionized to its H+, S2 state, it is sulfur through one of its gas states (hydrogen sulfide = H2S) which liberates oxygen from the oxides and silicates, oxygen was trapped in some 3.6 billion years ago. It is the purple sulfur bacteria which are earth's hardiest and oldest citizens, living in conditions (heat, salt, acidity, alkalinity) which would kill any other life form on the planet earth... ? We have identified a purple sulfur bacteria, which we believe to be the missing link, that is the first life form which established cooperative, covalent relationships with other uni-cellular competitors who were all trying to survive... ? The purple sulfur bacteria we have in mind, creates as it's output biochemical product,
glucose the universal energy and food source for all living entities. It is our speculation that this bacteria, which we shall call Chromatium, is the first life form to make a truce or treaty. Since Chromatium could produce glucose or food/energy sources for the other life forms, it attained a certain favored status, and would have been protected by the more powerful life forms who came to dependent on Chromatium's output for sustenance and vitality... ? DrKyia has reached the firm conclusion that the current double helix 4 code genetic primer is being decoded and interpreted improperly. This idea actually begain some 32 years ago in organic chemistry when drkyia just could not "grasp" the concepts. There did not seem to be any order or schemas to link the thousands and thousands of chemical reactions which drkyia had to memorize. When he took it a second time in summer school, the result was the same. Drkyia became so frustrated he literally tossed his organic chemistry book out his dorm window onto the busy street below, luckily no one was struck... ? Drkyia in analyzing the atomic organic elements, decided that carbon had to be the interface of the mental and physical processes, since carbon was the first atomic element to bond to itself, thus discerning some type of difference between itself as a solid entity with clear cut boundaries and edges. The C1-C2 bond is actually the foundation of organic chemistry so its made perfectly logical sense to drkyia that carbon was the beginning of the differentiation between an element and itself. We will show how this occurs, but carbon is just the physical implementation, sulfur is the controller, the signaler, the supervisor, the coordinator and uses the carbon high thermal tolerance to build the base of organic substrates on... ? So if a chromosome literally means light being where is the "light" part of the dna/rna/amino acid process. Drkyia believes that chromosomes and in fact the entire process of metabolism is driven by the dynamics of light, color and their heat or thermal content. For the only force which can break magnetic covalent bonds is heat which literally melts the crystalline lattice points, stretching them like taffy until the bond breaks. Drkyia believes the SH bond is the prime or primary organic covalent bond since SH is the first entity to be ionized and is the fuel used by Chromatium and his purple and green sulfur cousins. Drkyia believes in the Jungian process of synchronicity which means nothing happens by chance, so the fact that Chromosome, Chromatin, and Chromatium are so similar in name is an important clue in the solution to the gigantic jigsaw puzzle which makes up planets earth biosphere, which some scientists believe goes by the name of "Gia", which was articulated by one of our most intelligent NASA astronauts... ? .We have identified the oldest living carbon based life form on earth. This purple, anerobic sulphur bacteria "excretes" glucose as it's metabolic output. The bacterially made natural glucose is the key to understanding enzymes, proteins, and metabolic processes... ? What is the link between all these levels of abstraction, levels of structure and crystalline lattices, and in general an additive advancement from the smallest and oldest life forms on earth the cyanobacteria to the most evolved species on earth, homo sapiens, and the ? major metabolic pathways and biochemical reactions found throughout the human body...
? .Our triple helix, tri-polar genetic theory of evolution posits that since there is no evidence of the discontinuity of organic life on earth dating back to these same 2 billion year old sulfur and hydrogen based cyanobacteria must be the parents or first contributors to the planet earth genome... ? Medicine has convinced the lay public that side effects are "normal" and to be expected, but that is not the case; the jargon and scientific language and symbols these modern day ? Witch doctors hide behide do not allow the lay public the ? In every procesess on earth there is a beginning step, a first of a kind, a catalyst to facilitate a change of state. DrKyia, Chief Biomolecular Chemistry said in a recent interview by this scientific reporter. The things he told me were astounding. I did and could not believe what he was telling me. It was too revolutionary, too radical, for even the mere fact of the possibility? ? DrKyia told me that he has reliable scientific facts and evidence that the current double helix dna genetic coder, using (adenine=a, thymine = t, guanine= g; cytosine and uracil= U). These five nucleotide amino acid amino acid synthesis codons are missing one member of the nucleotide family. There should be 6 members in the family not 5 or even 4 as there is in the current standard WatsonCrick base pairing (A1-T1,G1-C1) = DNA; and in tRNA, uracil = U substitutes for T= Thymine. So the essential difference between DNA genetic nucleotide codes and RNA genetic codons is that uracil substitutes for thymine. You mean, U substitutes for T when dna instructs the cytoplasmic ribosome and mitochondrea bacterial organic work force to produce a certain of a certain chemical substance, namely, catalytic enzymatic polymorphic polypeptide proteins (P>270,000 daltons). Hey that a pretty big macromolecule I said to DrKyia. He replied, that is nothing to the fire fly genome I sequenced using my newly validated triple helix genetic primer... ? Yes, and the thinking is if science can dechper the genetic code then cellular repair and disease prevention will be possible. Will you get back to the double vs. triple helix cmpetition between the British team of Watson, Crick and other English "legitimate scientists". Are you implying Watson and Crick were not world class scientists? They must have been, they won the Nobel Prize didn't they? Yes they did drkyia said, but they won it because of scientific editorial suppression than true scientific validation. What in the world are you talking about I asked drkyia? ? Well the American team of Linaus Pauling of Cal Tech and his son had just two years previously won a noble prize for determing the alpha structure of the dna and rna molecules. You mean they figured out how proteins are naturally shaped when they are not under undue heat, pressure, or attack. Exactly, drkyia said. He said someday I might make a good scientist, I took that as a compliment, the first one he had ever given me in 3 years of working together... ? I asked the professor of organic chemistry to reconsider since I was very confused about the 64 three bit code primer call the genetic primer. How did you get the number 64 drkyia. Well since there are 4 nucleotides (technically A,U,G,C are tRNA ) codon codes... ? Critical to the entire thread of evidence is the number 6 and the letters "S" and "TH". You
will see as we take our journey from the atmosphere of Venus to the Jupiter moon, Ito. They both contain sulphur as does every important organic and inorganic compound known to man. We will show how each of the ? Periodic chart atomic elements play a key role in the healthy and fully functional species, called HomoSapiens. However, man has vastly underestimated the power of sulphur and this carelessness has and will create more viral and cancerous conditions... ? The current dna and rna codes only uses the first five atomic elements (H,C,N,O,P), the thrust of this paper attempts to demonstrate why Sulfur (SF) & Sulphur (SPH) belong in this select core group of basic atomic building blocks. We distinguish between Sulfur (SF) & Sulphur (SPH) on the of the two different organic processes the SF and SPH composites control. SF regulates the ? Thiol relationships, while SPH controls the more normal Phosphorylation interactions... ? Sulphur along with carbon predates human history. Because of its association with volcanic eruptions, hot molten smelly lava, and extremely acidic nature, has been associated with evil, as evidenced by the religious idiom, "Fire and brimstone . The brimstone refers to sulfur... ? An explanation is in order of course. Language is a man made invention while mathematics is not. Why is it that the first human languages from all our archaeological, anthropological, and carbon fourteen fossil dating records began from the right and written script proceeded from right to left. English, on the other hand, is written from left to right. Why is this important? Because the universal, cosmic magnetic flux river flow is counterclockwise that is, from right to left. The earth spins counterclockwise on its axis, the earth revolves counterclockwise around the sun in 366 days. Our weather patterns and jet streams ? move counterclockwise. Even opening most faucets requires counterclockwise motion. Clockwise is ? shutting off, choking, cutting off. That is was sulfur is doing to our dna codes, causing randomly generated mutations, retrograde viruses, and superstrains of bacteria which are immune to our most ? powerful strains of bacterial hybridized colonies... ? With hundreds if not thousands of pictures, schematic and diagrams, we we'll provide the most comprehensive analysis and documentation of all sulphur related organic and inorganic compounds... ? Drkyia in analyzing the atomic organic elements, decided that carbon had to be the interface of the mental and physical processes, since carbon was the first atomic element to bond to itself, thus discerning some type of difference between itself as a solid entity with clear cut boundaries and edges. The C1-C2 bond is actually the foundation of organic chemistry so its made perfectly logical sense to drkyia that carbon was the beginning of the differentiation between an element and itself. We will show how this occurs, but carbon is just the physical implementation, sulfur is the controller, the signaler, the supervisor, the coordinator and uses the carbon high thermal tolerance to build the base of organic substrates on... ? So if a chromosome literally means light being where is the "light" part of the dna/rna/amino
acid process. Drkyia believes that chromosomes and in fact the entire process of metabolism is driven by the dynamics of light, color and their heat or thermal content. For the only force which can break magnetic covalent bonds is heat which literally melts the crystalline lattice points, stretching them like taffy until the bond breaks. Drkyia believes the SH bond is the prime or primary organic covalent bond since SH is the first entity to be ionized and is the fuel used by Chromatium and his purple and green sulfur cousins. Drkyia believes in the Jungian process of synchronicity which means nothing happens by chance, so the fact that Chromosome, Chromatin, and Chromatium are so similar in name is an important clue in the solution to the gigantic jigsaw puzzle which makes up planets earth biosphere, which some scientists believe goes by the name of "Gia", which was articulated by one of our most intelligent NASA astronauts...
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I.742 lattice structures. Therefore, we are proposing adding a sixth nucleotide code = I for Inosine... A key two our discoveries has been our fortunate uncovering of the secret code and primer for the English language itself. Every language has certain primary or prime symbols or codes which are the foundation an infrastructure of the the neural network meaning association's. We are calling these memes or meaning codes. meaning codes are abstractions of abstractions. They are derivatives of the original meaning intent an overtime of the word or alpha code has been compressed and shortened to a level where a word has both denotative and connotative constructs. That is, there are two meanings or a word within a letter. We will demonstrate how this works the word skill, S, K, I, L,L is really the following: specialized, knowledge, insight, learned, language. Isnot this what a skill is, specialized knowledge, In working with DNA, scientists are working in magnitudes of 10 to the twenty seventh power or .0000000000000000000000000001. the average the DNA molecule might be 30 nm long. That is, 300 angstroms or hydrogen bonds. it is very difficult if not impossible to use English to describe such a small and quantity and and mixing the ingredients i.e. hydrogen, carbon etc. in the right proportions... I am looking to patent my new 6 code genetic primer which will be "nature's own" planet earth's genome of which mankind is certainly the most advanced... I am looking to find some suitable medications to compare my 6 code genetic primer to the current 4 code in synthesizing some simple molecular compounds such as "common aspirin" which is the most used pharmaceutical grade bioactive molecular compound I would like the opportunity to present my facts, logic and algorythmic proofs to an expert such as yourself. There are not many people in the world that can understand my work even though I documented every idea, concept, association link in both a time series story boad fashion as well as identifying the You probably have guessed this element by now but I hope you are intrigued enough to contact me... I need an expert such as yourself to "play devil's advocate" in locating flaws in my triple helix model... Thank you for your time and I hope to hear from you or one of your associates who might be more interested in this project, although I cannot see how any scientist Thank you for your time and I hope to hear from you or one of your associates who might be more interested in this project, although I cannot see how any scientist We will show how sulfur is the evolutionary thread and string which starts, stops, and controls each and every process step at every level of protein synthesis (i.e. methionine = AUG and Cysteine at the amino acid level, Acetyl Coenzyme A at the glycoprotein fatty acid level, SAM or S-Adenyl-methionine at the
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hormone or spermidine level, and Tformly met at the tRNA final genetic code instruction set level... The primary focus of this paper is to provide facts and logic in asserting that the dna genetic code i.e. the Watson-Crick double helix model of genetic code (codons) i.e. (adenine, thymine, guanine, cytosine = dna 4 codes) and adenine, uricidine, guanine, and cytosine = rna 4 codes). Please notice the esstential two differences in RNA and DNA The primary focus of this paper is to provide facts and logic in asserting that the dna genetic code, i.e. the Watson-Crick double helix model of genetic code (codons) i.e. (adenine, thymine, guanine, cytosine = dna 4 codes) and adenine, uricidine, guanine, and cytosine = rna 4 codes). Please notice the esstential two differences in RNA and DNA Specified is the simple mathematical operation of addition. You will note that each of the vector strings with 6 codons (A1,T1,G1,C1,I1,U1) and (U2,I2,C2,G2,T2,A2) add up to 7. That is the adenine 1 added to the adenine 2 codon code adds up to 7 i.e. 1+6=7... In every procesess on earth there is a beginning step, a first of a kind, a catalyst to facilitate a change of state. DrKyia. Chief Biomolecular Chemistry said in a recent interview by this scientific reporter. The things he told me were astounding. I did and could not believe what he was telling me. It was too revolutionary, too radical, for even the mere fact of the possibility? DrKyia told me that he has reliable scientific facts and evidence that the current double helix dna genetic coder, using (adenine=a, thymine.= t, guanine= g; cytosine and uracil U). These five nucleotide amino acid amino acid synthesis codons are missing one member of the nucleotide family. There should be 6 members in the family not 5 or even 4 as there is in the current standard Watson-Crick base pairing (A1-T1,G1-C1) = DNA; and in tRNA, uracil = U substitutes for T= Thymine. So the essential difference between DNA genetic nucleotide codes and RNA genetic codons is that uracil substitutes for thymine. You mean, U substitutes for T when dna instructs the cytoplasmic ribosome and mitochondrea bacterial organic work force to produce a certain of a certain chemical substance, namely, catalytic enzymatic polymorphic polypeptide proteins (P>270,000 daltons). Hey that a pretty big macromolecule I said to DrKyia. He replied, that is nothing to the fire fly genome I sequenced using my newly validated triple helix genetic primer... DrKyia.told me that he has reliable scientific facts and evidence that the current double helix dna genetic coder, using (adenine=a, thymine.= t, guanine= g; cytosine and uracil U). These five nucleotide amino acid amino acid synthesis codons are missing one member of the nucleotide family. There should be 6 members in the family not 5 or even 4 as there is in the current standard Watson-Crick base pairing (A1-T1,G1-C1) = DNA; and in tRNA, uracil = U substitutes for T= Thymine. So the essential difference between DNA genetic nucleotide codes and RNA genetic codons is that uracil substitutes for thymine. You mean, U substitutes for T when dna instructs the cytoplasmic ribosome and mitochondrea bacterial organic work force to produce a certain of a certain chemical substance, namely, catalytic enzymatic polymorphic polypeptide proteins (P>270,000 daltons). Hey that a pretty big macromolecule I said to DrKyia. He replied, that is nothing to the fire fly genome I sequenced using my newly validated triple helix genetic primer...
What are you talking about DrKyia? Do you remember when I told you that story about Linaus Pauling and the triple helix? Briefly, please refresh mymemory, well, Dr. Linaus Pauling, America's greatest scientist, was working on his own version of the dna primer. He was competing in a friendly rivalry, so he thought, against Drs.Watson and Crick. Not the same guys who won the nobel prize for their elucidation of the double helix structure of the dna molecule. Yes, those are the chaps who won acclaim for the work done by many other scientist, far smarter than Crick and especially the buffoon Watson, who flunked out of two graduate level biology program before landing at Cambridge England, and in the lab of Dr. Francis Crick, the real brains behind the scientific problem solving and the crystallography work which determined the number of base pairing in each helix (3.6). This task required good spatial, 3D, geometrical and cognitive visualization skills. That is Crick was able to visualize in his mind what a shape, in this case a double helix which looks like a twisted step ladder to drkyia. Crick was like an analog CAD in that he could manipulate (X,Y,Z = width, length, depth) 3 dimensional structure very well. Drkyia said he found Origiami paper folding polyhedron modeling much easier and reliable. Any way, where were we... Drkyia went on to say there are 14 3 dimensional possible structures proteins could have. How did he come up with that number, I asked? He said, in 1848 a certain Theodore Bravais, drew all the possible three dimensional shapes the face, body and point symmetry shapes could assume. He came up with 14 distinct crystalline shapes. No more, no less. How does that relate to molecular biology I asked. Well biological molecules which are aggregations of cells with various shapes and sizes all fall within these 14 structures. And why is structure important? Because function follows structure drkyia said. The shape is the solution. I felt I had intruded enough from his endless theorizing so I dedcided to go back and do some more research on this double and triple helix thing... Drkyia went on to say there are 14 3 dimensional possible structures proteins could have. How did he come up with that number, I asked? He said, in 1848 a certain Theodore Bravais, drew all the possible three dimensional shapes the face, body and point symmetry shapes could assume. He came up with 14 distinct crystalline shapes. No more, no less. How does that relate to molecular biology I asked. Well biological molecules which are aggregations of cells with various shapes and sizes all fall within these 14 structures. And why is structure important? Because function follows structure drkyia said. The shape is the solution. I felt I had intruded enough from his endless theorizing so I dedcided to go back and do some more research on this double and triple helix thing... So who won I asked. Who do you think dummy, is the genetic code called the double or triple helix model... lattice structures. Therefore, we are proposing adding a sixth nucleotide code = I for As we will see later, I provides iron, iodide and even oxygen to protein synthesis... Will you please state your name for the record. My name is Dr John Allen Berger and I am a
scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years We aim to show you that inosine Monophosphate or I M.P. was indeed the first purine nucleotide closed ring of structure created by nature through our natural selection and Inheritance Mechanisms Which Value economy and the efficiency as criteria for survival and hardness and opposed to Extinction because a less costly energy solution which is always a E Molecular Crystalline Structure and and there is always competition between competing at Structures to occupy the role or position which is critical to the survival of the host organism and ecologies of other Chromosomes which adds Symbion Likely developed very efficient communication messaging systems which allow very quick response time to threats or unknown hazards. The prime directive imbedded in each and Cell and each DNA molecule is that survival aholt is greater in any single individual because if the whole host does not survive the nine of the smaller Organizational units such as the Organs Tissues and even cells will not survive. There And the reason I am the first common Symbiotic Uni Cellular organism which contributed to his or RNA to the planet earth's genome of which the human genome is by far the most complex and Advanced through the expansion and growth of Neocortex which is the most dance networked PhotoChemical Crystalline Lattice structure ever developed on earth. Man's consciousness is the defining difference which separates Homo sapiens from all other species and N and it is this ability to Abstracts and generalize from specific unique situations to similar situations but with significant variances which make the two situations totally different... I believe and will to demonstrate both logically and empirically of the merits of my arguments and assertions. Necessarily, much of what you will see defies "mainstream double helix
science", We have concluded that every process has a beginning, even the universe (i.e. "bigbang" theory), so that the atomic elements especially the central character roles of hydrogen1, carbon12, nitrogen14, oxgyen16, phosphorous31. This is where the current dna double helix theory stops in assigning these 5 atomic elements to the status of "the organic big five". The triple helix adds sulfur to the list of 5 making it the sixth and last organic atomic element. Therefore, just as in "Genesis" in the Old Testament, "God made heaven and earth in six days (not five days) and rested on the seventh." 4200 apples, oranges, and bannas and everyone of those 3 natural fruits making each of the 4200 people who ate the fruit sick. I will tell you those odds, they are 100 billion to 1. That is 100,000,000,000 to 1. There is one chance in 100 billion that all 4200 people eating those 3 fruits will get sick of have a "side effect". But you might counter and say, oranges are not medicines, they are not as powerful nor are they intended to be. And you would be right. But this is the precise reason we must validate for the first time the double helix theory of medicinal genomics. The fact every product from every factory all over the entire world cannot produce one organic product which is not defective as defined by the "term" "side effect"; a side effect is a defect in the Novagon Triple Helix model of genetic evolution... I have constructed a 6 code tRNA amino acid primer, adding two nucleotide codes to the present tRNA genetic code. These two additional nucleotide codes should have never been omitted... Every final product ever made using the current genetic code causes toxic side effects (i.e. prescription drug is defective, causes unexpected, uncontrollable side effects from mild dizziness to 106,000 fatalities in 1999). Side effects are "not a normal part of the drug discovery process); if you take a nature made protein like biotin or any of the other vitamin macromolecules in the right dosage you don't get side effects... Why am I going into Photosynthesis and Light and electronic Cycles and Circuits, in is because these are the ultimate power sources of life itself. A end it is only when Evolution created a closed ring since inosine Monophosphate or I M.P. was the first purine nucleotide to have a closed ring structure, it is the acknowledged parent and precursor to the other two purines that are now in the genetic code i.e Adenosine Monophosphate and guanosine monophosphate, if it would seem a to be a grave mistake of not including inosine Monophosphate as the third and last purine nucleotide in Natures Genetic Code... since inosine Monophosphate or I M.P. was the first purine nucleotide to have a closed ring structure, it is the acknowledged parent and precursor to the other two purines that are now in the genetic code i.e Adenosine Monophosphate and guanosine monophosphate, if it would seem a to be a grave mistake of not including inosine Monophosphate as the third and last purine nucleotide in Natures Genetic Code... Let's Return to the closed Purine ring issue and try to anticipate what might occur if purine it synthesis de novo is short its starting molecular structure namely I M.P. or inosine Monophosphate. And apt analogy might be comparing inosine Monophosphate to the Starter
of an automobile which consists of some 3500 different parts. while is true that the Starter is only one part it certainly is a critical part, if the starter does not perform its function than the other 3499 Parts are in essence nicely assembled pieces of junk, and the purpose of the automobile to transport will no longer be possible sense the engine and drive train have no power. After the automobile is started, the starter becomes less important since the engine is running and the transportation function can occur. In the human and it cellular metabolism once the organism has been born the " engine " has already been started and is never turned off until the death of the cell for the host organism Occurs. So, is it is difficult to measure the impact of being out the Starter for making closed Purine rings " from scratch " but since 70 percent of purine nucleotides are made de novo and only 30% are made from salvage or recycling of already used purine bases, sugars, and phosphates, if is clearly evident that this 70% is going to have a major impact in the synthesis of DNA and RNA, amino acids and proteins, and most likely glucogenic and Glycolysis to critical energy pathways and cycles. It is also likely to impact Fatty Acid Synthesis Sense to of the major Citric Acid molecule's, fumurate and succinate, as well as the urea cycle which eliminates toxic ammonia from our Glutamate excitatory Neurotransmitters and/or serotonin intermediates... Underlies the current central THEORY Dogma the triple helix model of evolutionary development includes the synthesis and degradation of the proteins to other partners i.e. Lipids and carbohydrates are encoded in the DNA nucleic acid structure which is essentially Purine and Pyrimidine Metabolism. The genetic code codes for every metabolic pathway and every metabolic cycle, the proteins might be the physical labors but those Labor Hrs also need ENERGY and Nutrition and Lipid Substrates to build a physical Tissues as well as the hormonal class of molecule which communicate at a " lower-level " of evolutionary development but one in which the organism cannot function or survive without. This Organic Infrastructure is a coordinated through the RNA and DNA Purine and Pyrimidine Nucleotides but especially their atomic level side chains i.e. NH2, C H three... Underlies the current central THEORY Dogma the triple helix model of evolutionary development includes the synthesis and degradation of the proteins to other partners i.e. Lipids and carbohydrates are encoded in the DNA nucleic acid structure which is essentially Purine and Pyrimidine Metabolism. The genetic code codes for every metabolic pathway and every metabolic cycle, the proteins might be the physical labors but those Labor Hrs also need ENERGY and Nutrition and Lipid Substrates to build a physical Tissues as well as the hormonal class of molecule which communicate at a " lower-level " of evolutionary development but one in which the organism cannot function or survive without. This Organic Infrastructure is a coordinated through the RNA and DNA Purine and Pyrimidine Nucleotides but especially their atomic level side chains i.e. NH2, C H three... The strategy of controlling I M.P. CH2 to control the production of the guanosine which it the cancer cancerous cell uses to grow more rapidly and produce more clones of itself. By suppressing the I M.P. not as much she M.P. will be made and the cancer cannot grow as fast, at least that is the thinking. However, unbeknown to the medical and Biochemical Scientists is it the regulatory impact this will have on the synthesis of ATP Sense IM PEA 1 is the gene
which controls the synthesis of adenosine Succinate, the first adenine it intermediate formed after I M.P. and its closed Purine ring structure became the foundation and it substrate for purine metabolism. The current Purine Metabolic THEORY is there is no connection between im P1 and I am p to which is the same as saying there is no connection between the left arm and the right arm. Technically from a purely physical Spatial point of view this assumption might be correct but sense the two arms are coordinated and Mediated by the cerebellum which does connect the left and right arms in the overall schema of Arm Usage, if it might be prudent to follow the lead of Nature and her volutionary growth and interconnectedness Pattern The strategy of controlling I M.P. CH2 to control the production of the guanosine which it the cancer cancerous cell uses to grow more rapidly and produce more clones of itself. By suppressing the I M.P. not as much she M.P. will be made and the cancer cannot grow as fast, at least that is the thinking. However, unbeknown to the medical and Biochemical Scientists is it the regulatory impact this will have on the synthesis of ATP Sense IM PEA 1 is the gene which controls the synthesis of adenosine Succinate, the first adenine it intermediate formed after I M.P. and its closed Purine ring structure became the foundation and it substrate for purine metabolism. The current Purine Metabolic THEORY is there is no connection between im P1 and I am p to which is the same as saying there is no connection between the left arm and the right arm. Technically from a purely physical Spatial point of view this assumption might be correct but sense the two arms are coordinated and Mediated by the cerebellum which does connect the left and right arms in the overall schema of Arm Usage, if it might be prudent to follow the lead of Nature and her volutionary growth and interconnectedness Pattern The strategy of controlling I M.P. CH2 to control the production of the guanosine which it the cancer cancerous cell uses to grow more rapidly and produce more clones of itself. By suppressing the I M.P. not as much she M.P. will be made and the cancer cannot grow as fast, at least that is the thinking. However, unbeknown to the medical and Biochemical Scientists is it the regulatory impact this will have on the synthesis of ATP Sense IM PEA 1 is the gene which controls the synthesis of adenosine Succinate, the first adenine it intermediate formed after I M.P. and its closed Purine ring structure became the foundation and it substrate for purine metabolism. The current Purine Metabolic THEORY is there is no connection between im P1 and I am p to which is the same as saying there is no connection between the left arm and the right arm. Technically from a purely physical Spatial point of view this assumption might be correct but sense the two arms are coordinated and Mediated by the cerebellum which does connect the left and right arms in the overall schema of Arm Usage, if it might be prudent to follow the lead of Nature and her volutionary growth and interconnectedness Pattern The strategy of controlling I M.P. CH2 to control the production of the guanosine which it the cancer cancerous cell uses to grow more rapidly and produce more clones of itself. By suppressing the I M.P. not as much she M.P. will be made and the cancer cannot grow as fast, at least that is the thinking. However, unbeknown to the medical and Biochemical Scientists is it the regulatory impact this will have on the synthesis of ATP Sense IM PEA 1 is the gene which controls the synthesis of adenosine Succinate, the first adenine it intermediate formed after I M.P. and its closed Purine ring structure became the foundation and it substrate for purine metabolism. The current Purine Metabolic THEORY is there is no connection between im P1 and I am p to which is the same as saying there is no connection
between the left arm and the right arm. Technically from a purely physical Spatial point of view this assumption might be correct but sense the two arms are coordinated and Mediated by the cerebellum which does connect the left and right arms in the overall schema of Arm Usage, if it might be prudent to follow the lead of Nature and her volutionary growth and interconnectedness Pattern Will the Hearing please come to order. Your Honor I like to address the court in the matter of Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular We aim to show you that inosine Monophosphate or I M. P. was indeed the first purine And the reason I am the first common Symbiotic Uni Cellular organism which contributed to his tell us then what was it like we were first created / an Bit I was not the first bacterial or life of First all all, you would not believe the conditions we lived under . I happened to be lucky in I will never forget that day you when I was almost eaten by two of the meanest and largest I will never forget that day you when I was almost eaten by two of the meanest and largest about to eat the meat me when I said stop one moment please. You two guys must be of very must be hungry since you want me to eat me? Is this not correct last I asked? They both replied they were very hungry and I said let me give you a sample of what I produce which I think you'll they were very hungry and I said let me give you a sample of what I produce which I think you'll they were very hungry and I said let me give you a sample of what I produce which I think you'll like. Well I happen to have a small amount of glycogen Stored and I gave those to predators like. Well I happen to have a small amount of glycogen Stored and I gave those to predators but I stated I had no more sense I could only make small amounts over long periods of time... predatory Organisms I would share by Glucose with them on a daily bases basis in addition, I predatory Organisms I would share by Glucose with them on a daily bases basis in addition, I That is quite a story Dr Chromatium, and how can you proof its true. Colwell if I can call to the ridiculous statement I have ever erred said the judge's. Sulfur is but a minor element who quite Well I gues I better begin writing the text to this scientific opus. Deep within ourselves is a Well I gues I better begin writing the text to this scientific opus. Deep within ourselves is a power that only a belieer can witness. I have immersed myself in this scientifaic knowledge power and have come up with some very unsual theories and concepts. I believe everyone will The immense implications our over whelming if I am correct and I believe I am at least 90% The immense implications our over whelming if I am correct and I believe I am at least 90% The immense implications our over whelming if I am correct and I believe I am at least 90% It has taken me since 1969 to prove to myself that I was not wrong about my perception at that I believe and will to demonstrate both logically and empirically of the merits of my arguments We have concluded that every process has a beginning, even the universe (i.e. "big-bang" 4200 people who ate the fruit sick. I will tell you those odds, they are 100 billion to 1. That is compounds (i.e. fructose, mannose, glucose) which share this same C6H12O6 chemical theory, I am looking for the progenitor of organic life on earth. There had to be a first which instruction sets of the various orgaic work force (i.e. mitochondrea, pepsins, globins, vitamins,
I have constructed a 6 code tRNA amino acid primer, adding two nucleotide codes to the Every final product ever made using the current genetic code causes toxic side effects (i.e... Why am I going into Photosynthesis and Light and electronic Cycles and Circuits, in is because since inosine Monophosphate or I M.P. was the first purine nucleotide to have a closed ring the genetic code i.e Adenosine Monophosphate and guanosine monophosphate, if it would synthesis de novo is short its starting molecular structure namely I M.P. or inosine development includes the synthesis and degradation of the proteins to other partners i.e. Lipids their atomic level side chains i.e. NH2, C H three... The strategy of controlling I M.P. CH2 to control the production of the guanosine which it the suppressing the I M.P. not as much she M.P. will be made and the cancer cannot grow as fast, controls the synthesis of adenosine Succinate, the first adenine it intermediate formed after I and I am p to which is the same as saying there is no connection between the left arm and the First, inosine is the parent purine to adenine and guanine. Inosine is the first linearized chain of amino acids.to form a closed ring i.e. purine. Without inosine there would be no organic aromatic heterocyclic compounds. There would be just long chains of amino acids... The substitution mathematical operator (i.e. Uracil (U) for Thymine (T) is a Purine Nucleotide Anabolic to Catabolic Cycle Switch A to I Deaminase Nature??s Ingenious 3 bit Codon even Codes for bi-lateral Symmetry (i.e. left and Nature??s Ingenious 3 bit Codon even Codes for bi-lateral Symmetry (i.e. left and cellular organelles i.e. mitochdondria, ribosomes The entire concept of inheritance and evolution rests on "new generations" (i.e... I believe and will to demonstrate both logically and empirically of the merits of my arguments and assertions. Necessarily, much of what you will see defies "mainstream double helix science", We have concluded that every process has a beginning, even the universe (i.e. "bigbang" theory), so that the atomic elements especially the central character roles of hydrogen1, carbon12, nitrogen14, oxgyen16, phosphorous31. This is where the current dna double helix theory stops in assigning these 5 atomic elements to the status of "the organic big five". The triple helix adds sulfur to the list of 5 making it the sixth and last organic atomic element. Therefore, just as in "Genesis" in the Old Testament, "God made heaven and earth in six days (not five days) and rested on the seventh." 4200 apples, oranges, and bannas and everyone of those 3 natural fruits making each of the 4200 people who ate the fruit sick. I will tell you those odds, they are 100 billion to 1. That is 100,000,000,000 to 1. There is one chance in 100 billion that all 4200 people eating those 3 fruits will get sick of have a "side effect". But you might counter and say, oranges are not medicines, they are not as powerful nor are they intended to be. And you would be right. But this is the precise reason we must validate for the first time the double helix theory of medicinal genomics. The fact every product from every factory all over the entire world cannot produce one organic product which is not defective as defined by the "term" "side effect"; a side effect is a defect in the Novagon Triple Helix model of genetic evolution... To recap, the current DNA model has four DNA codes.and four RNA codes, in actuality there
are five DNA/RNA nucleotide codes. Adenine always bonds due thymine in the DNA phase, while guanine always bonds and cytosine. The difference between the DNA and RNA in that Uricidine substitutes for thymine in the final compiled instruction set which.is the final formulation or "recipe" used to construct To recap, the current DNA model has four DNA codes and four RNA codes, in actuality there are five DNA/RNA nucleotide codes. Adenine always bonds due thymine in the DNA phase, while guanine always bonds and cytosine. The difference between the DNA and RNA in that Uricidine substitutes for thymine in the final compiled instruction set which.is the final formulation or "recipe" used to construct To recap, the current DNA model has four DNA codes and four RNA codes, in actuality there are five DNA/RNA nucleotide codes. Adenine always bonds due thymine in the DNA phase, while guanine always bonds and cytosine. The difference between the DNA and RNA in that Uricidine substitutes for thymine in the final compiled instruction set which.is the final formulation or "recipe" used to construct To recap, the current DNA model has four DNA codes and four RNA codes, in actuality there are five DNA/RNA nucleotide codes. Adenine always bonds due thymine in the DNA phase, while guanine always bonds and cytosine. The difference between the DNA and RNA in that Uricidine substitutes for thymine in the final compiled instruction set which.is the final formulation or "recipe" used to construct The Novagon triple helix DNA model uses the mathematical operation of the addition rather than substitution in the DNA RNA amino acid protein production process. Instead of substituting uricidine for thymine, the triple helix model adds a six and final nucleotide called Inosine. The the double and triple helix models you different mathematical operations to transmit the DNA instruction sets to the organic workers who implement and execute the RNA genetic primer... and Francis Crick in 1953. the metaphors which the English scientists at described the computer enhanced digitized image are very telling in how the DNA data structure is organized and processed. Looking at the current DNA databases a available on the Internet, one sees the current DNA codons which are three of the four possible nuclear tide codes for synthesizing one of the 20 natural amino acids. A twisted double Helix is not a true three dimensional structure, but instead a non-repeating 2 dimensional matrix. (i.e. the three codons are x1,y1,x2. a true three dimensional structure would have and Francis Crick in 1953. the metaphors which the English scientists at described the computer enhanced digitized image are very telling in how the DNA data structure is organized and processed. Looking at the current DNA databases a available on the Internet, one sees the current DNA codons which are three of the four possible nuclear tide codes for synthesizing one of the 20 natural amino acids. A twisted double Helix is not a true three dimensional structure, but instead a non-repeating 2 dimensional matrix. (i.e. the three codons are x1,y1,x2. a true three dimensional structure would have and Francis Crick in 1953. the metaphors which the English scientists at described the computer enhanced digitized image are very telling in how the DNA data structure is organized and processed. Looking at the current DNA databases a available on the Internet, one sees the current DNA codons which are three of the four possible nuclear tide codes for synthesizing one of the 20 natural amino acids. A twisted double Helix is not a true three dimensional structure, but instead a non-repeating 2 dimensional matrix. (i.e. the three codons are x1,y1,x2. a true three dimensional structure would have In fact, drkyia rates
file:///C:/Users/dr%20john%20allen%20berger/Des...455812393412.berger_original_writings2.txt.htm (10 of 18) [4/27/2008 12:25:24 AM]
symmetry as one of the fundamental design principles in his triple helix tri-polar theory of evolution, a big part of which is the rna/dna/rna/amino acid/protein/enzyme processes. Drkyia noted there was only one start or initiator in the amino acid synthesis process but three stop codes, and those three codes were not instruction sets to build any type of polypeptide protein. There were 64 total genetic codes, and only 20 final products (20 protein amino acids - common) . 61/20 = 3.05 codes for every one product. What did .05 of an amino acid mean anyway. Which part of the dna does the .05 come from the phosphate-backbone, the ribonucleic pentose sugar or the purine or pyramidine base. Drkyia said that nature in 5 billion years would develop a more efficient coding scheme than this, and thus has produced his own version of the genetic code which happens to expand the amino acid class from only proteins to the fatty acids and complex sugars ( polysaccyrides). He ended up with 27 amino acids which formed a closed loop network of the various metabolic cycles which enabled the organic uni-cellular work force of bacteria, yeast, algae and other microbes to obtain the nutrients (glucose) they needed to perform their specialized function of producing a very specific molecule which was a small but important "cog" in the organism as a whole, in this case, the species, homo-sapiens, Please note that sulfur is not currently considered one of the "big five" of organic atoms. Novagon DNA has added Sulfur to the present "big five"s isotopes (H1,H2, C12,C13,N14,N15,O16,O18,O17,P31,S32,S34,S33,S36)... In addition, since rna is "older" than dna and is the last "just in time" amino acid manurfacturing codes it is the most important. DNA is a test validation stage where the original order = rna1 splits into 2 sequences for validation purposes. One string of nucleotide codes (ie. ATGCIU) spirals counterclockwise (magnetically positive quantum spin director) and the second complementary sequence string (UICGTA) proceeds in a clockwise negatively charged direction. Thus the rna genetic code in validated in the dna phase when the 6 codes which actually are 6/2 = 3 codes which instruct the ribosomes, mitochondrea and other celluar organic work force which structure to build in maintaing a bilateral symmetry such as the mirror images of our hands, feet and eyes. These organs and body parts are exactly the same only reversed in sequence. The two strands of dna when the meet at the node or plant location where the amino acid polypeptide molecule is to be produced , have a very simple validation step to insure fidelity of the amino acid production order . If the sequences are number A=1, T=2, G=3, C=4, I=5 and U=6, then one strand will be sequenced by 1,2,3,4,5,6; the second sequence will be 6,5,4,3,2,1; the mirror image or complement of the initial 1,2,3,4,5,6 strand. When these two strands meet at the specified node the validity test to validate that the right codon are being In addition, since rna is "older" than dna and is the last "just in time" amino acid manurfacturing codes it is the most important. DNA is a test validation stage where the original order = rna1 splits into 2 sequences for validation purposes. One string of nucleotide codes (ie. ATGCIU) spirals counterclockwise (magnetically positive quantum spin director) and the second complementary sequence string (UICGTA) proceeds in a clockwise negatively charged direction. Thus the rna genetic code in validated in the dna phase when the 6 codes which actually are 6/2 = 3 codes which instruct the ribosomes, mitochondrea and other celluar organic work force which structure to build in maintaing a bilateral symmetry such as the mirror images of our hands, feet and eyes. These
organs and body parts are exactly the same only reversed in sequence. The two strands of dna when the meet at the node or plant location where the amino acid polypeptide molecule is to be produced , have a very simple validation step to insure fidelity of the amino acid production order . If the sequences are number A=1, T=2, G=3, C=4, I=5 and U=6, then one strand will be sequenced by 1,2,3,4,5,6; the second sequence will be 6,5,4,3,2,1; the mirror image or complement of the initial 1,2,3,4,5,6 strand. When these two strands meet at the specified node the validity test to validate that the right codon are being In addition, since rna is "older" than dna and is the last "just in time" amino acid manurfacturing codes it is the most important. DNA is a test validation stage where the original order = rna1 splits into 2 sequences for validation purposes. One string of nucleotide codes (ie. ATGCIU) spirals counterclockwise (magnetically positive quantum spin director) and the second complementary sequence string (UICGTA) proceeds in a clockwise negatively charged direction. Thus the rna genetic code in validated in the dna phase when the 6 codes which actually are 6/2 = 3 codes which instruct the ribosomes, mitochondrea and other celluar organic work force which structure to build in maintaing a bilateral symmetry such as the mirror images of our hands, feet and eyes. These organs and body parts are exactly the same only reversed in sequence. The two strands of dna when the meet at the node or plant location where the amino acid polypeptide molecule is to be produced , have a very simple validation step to insure fidelity of the amino acid production order . If the sequences are number A=1, T=2, G=3, C=4, I=5 and U=6, then one strand will be sequenced by 1,2,3,4,5,6; the second sequence will be 6,5,4,3,2,1; the mirror image or complement of the initial 1,2,3,4,5,6 strand. When these two strands meet at the specified node the validity test to validate that the right codon are being In addition, since rna is "older" than dna and is the last "just in time" amino acid manurfacturing codes it is the most important. DNA is a test validation stage where the original order = rna1 splits into 2 sequences for validation purposes. One string of nucleotide codes (ie. ATGCIU) spirals counterclockwise (magnetically positive quantum spin director) and the second complementary sequence string (UICGTA) proceeds in a clockwise negatively charged direction. Thus the rna genetic code in validated in the dna phase when the 6 codes which actually are 6/2 = 3 codes which instruct the ribosomes, mitochondrea and other celluar organic work force which structure to build in maintaing a bilateral symmetry such as the mirror images of our hands, feet and eyes. These organs and body parts are exactly the same only reversed in sequence. The two strands of dna when the meet at the node or plant location where the amino acid polypeptide molecule is to be produced , have a very simple validation step to insure fidelity of the amino acid production order . If the sequences are number A=1, T=2, G=3, C=4, I=5 and U=6, then one strand will be sequenced by 1,2,3,4,5,6; the second sequence will be 6,5,4,3,2,1; the mirror image or complement of the initial 1,2,3,4,5,6 strand. When these two strands meet at the specified node the validity test to validate that the right codon are being DrKyia told me that he has reliable scientific facts and evidence that the current double helix dna genetic coder, using (adenine=a, thymine = t, guanine= g; cytosine and uracil= U). These five nucleotide amino acid amino acid synthesis codons are missing one member of the nucleotide family. There should be 6 members in the family not 5 or even 4 as there is in the current standard Watson-Crick base pairing (A1-T1,G1C1) = DNA; and in tRNA, uracil = U substitutes for T= Thymine. So the essential difference
between DNA genetic nucleotide codes and RNA genetic codons is that uracil substitutes for thymine. You mean, U substitutes for T when dna instructs the cytoplasmic ribosome and mitochondrea bacterial organic work force to produce a certain of a certain chemical substance, namely, catalytic enzymatic polymorphic polypeptide proteins (P>270,000 daltons). Hey that a pretty big macromolecule I said to DrKyia. He replied, that is nothing to the fire fly genome I sequenced using my newly validated triple helix genetic primer... However, The Novagon DNA triple helix model bears little resemblance to the original model and in fact we can never obtain a copy to check it out. Novagon DNA in a much more than a DNA primer it is an integration of all life sciences from the organic atomic The current the DNA model is composed of 4 nucleotide molecules named: adenine, substituted for thymine when DNA is transformed into RNA which of the final genetic To recap, the current DNA model has four DNA codes and four RNA codes, in actuality To recap, the current DNA model has four DNA codes and four RNA codes, in actuality DNA phase, while guanine always bonds and cytosine. The difference between the DNA DNA phase, while guanine always bonds and cytosine. The difference between the DNA The Novagon triple helix DNA model uses the mathematical operation of the addition rather than substitution in the DNA RNA amino acid protein production process. Instead operations to transmit the DNA instruction sets to the organic workers who implement sixth DNA element which we are proposing to elevate and join hydrogen, carbon, current Watson Crick DNA double helix model, uracil is substituted for thymine which occupied by the second and last nitrogen on the 6 sided hexagon dna base of C4,N2. We before sulfur arrived on earth, the dna hexagonal base was C3N3, a very balanced, symmetrical shape which nature seems to prefer. The fact the human dna base has lost shutting off, choking, cutting off. That is was sulfur is doing to our dna codes, causing In working with DNA, scientists are working in magnitudes of 10 to the twenty seventh power or .0000000000000000000000000001. the average the DNA molecule might be 30 computer enhanced digitized image are very telling in how the DNA data structure is organized and processed. Looking at the current DNA databases a available on the Internet, one sees the current DNA codons which are three of the four possible nuclear the dna does the .05 come from the phosphate-backbone, the ribonucleic pentose sugar or Novagon DNA has added Sulfur to the present "big five"s isotopes body which has its own genetic dna and rna code. It differs from the nucleic dna and rna body which has its own genetic dna and rna code. It differs from the nucleic dna and rna of the cell to the cytoplasm and finally to the nucleus itself where the DNA or genetic The primary focus of this paper is to provide facts and logic in asserting that the dna (adenine, thymine, guanine, cytosine = dna 4 codes) and adenine, uricidine, guanine, and cytosine = rna 4 codes). Please notice the esstential two differences in RNA and DNA First, U= Uracicidine substitutes for T= Thymine in the transcription phase of DNA to RNA and secondly the deoxy (dna) is more stable than the (rna) because it lacks the In addition, since rna is "older" than dna and is the last "just in time" amino acid manurfacturing codes it is the most important. DNA is a test validation stage where the clockwise negatively charged direction. Thus the rna genetic code in validated in the dna and body parts are exactly the same only reversed in sequence. The two strands of dna helix dna genetic coder, using (adenine=a, thymine = t, guanine= g; cytosine and uracil= 4 as there is
in the current standard Watson-Crick base pairing (A1-T1,G1-C1) = DNA; DNA genetic nucleotide codes and RNA genetic codons is that uracil substitutes for thymine. You mean, U substitutes for T when dna instructs the cytoplasmic ribosome and Pauling, America's greatest scientist, was working on his own version of the dna primer... of the dna molecule. Yes, those are the chaps who won acclaim for the work done by research centers competing with each other to solve the shape and structure of the dna previously won a noble prize for determing the alpha structure of the dna and rna saw the photographs of Bonnie Franklin's alpha and beta dna helices which she had dna standard code and standard molecular structures, a rather odd thing happened. The sulfur photochemicals, dna and the six code genetic primer The nucleotide molecular structure is a very special structure because it is the foundation of the DNA and RNA nucleic acids which archives each and every cells Total Genome, which is a catalog of all the genes or sequences of Purine and Pyrimidine Nucleotides which are the actual Molecular Structures referred to in the genetic code. It is through Purine and Pyrimidine Metabolism that DNA and RNA are formed and produced. The purine molecular structure is of larger than the pyrimidine and unlike the pyrimidine closed ring the purine ring is never destroyed while Cell is still functioning properly. Rivera The nucleotide molecular structure is a very special structure because it is the foundation of the DNA and RNA nucleic acids which archives each and every cells Total Genome, which is a catalog of all the genes or sequences of Purine and Pyrimidine Nucleotides which are the actual Molecular Structures referred to in the genetic code. It is through Purine and Pyrimidine Metabolism that DNA and RNA are formed and produced. The purine molecular structure is of larger than the pyrimidine and unlike the pyrimidine closed ring the purine ring is never destroyed while Cell is still functioning properly. Rivera We aim to show you that inosine Monophosphate or I M.P. was indeed the first purine nucleotide closed ring of structure created by nature through our natural selection and Inheritance Mechanisms Which Value economy and the efficiency as criteria for survival and hardness and opposed to Extinction because a less costly energy solution which is always a E Molecular Crystalline Structure and and there is always competition between competing at Structures to occupy the role or position which is critical to the survival of the host organism and ecologies of other Chromosomes which adds Symbion Likely developed very efficient communication messaging systems which allow very quick response time to threats or unknown hazards. The prime directive imbedded in each and Cell and each DNA molecule is that survival aholt is greater in any single individual because if the whole host does not survive the nine of the smaller Organizational units such as the Organs Tissues and even cells will not survive. There We are hereby asserting that the current WatsonCrick Genetic Primer with the four dna codes of (adenine, thymine, guanine, cytosine), and the out put 4 rna nucleotide codes of (adenosine, uracil, guanine, and cytosine, You will note that the most apparent different between the genetic primers in the double helix model is the substitution of uracil for thymine in the appropriate Chargraff base pairings (A-T, G-C in DNA, (A-U,G-C) in RNA... We are hereby asserting that the current Watson-Crick Genetic Primer with the four dna codes of (adenine, thymine, guanine, cytosine), and the out put 4 rna nucleotide codes of
(adenosine, uracil, guanine, and cytosine, You will note that the most apparent different between the genetic primers in the double helix model is the substitution of uracil for thymine in the appropriate Chargraff base pairings (A-T, G-C in DNA, (A-U,G-C) in RNA... an i/o management psychologist, and in the last five years devoted all my energies to the dna code double helix theory of dna and its subsequent production of the 20 natural amino The "correct and valid dna codes have 6 codes not 4". I am in the process of "patenting" the new 6 digit dna primer codes which will be validated when they an apple you don't have a side effect. The dna codes are wrong and these for if I am right, the current 4 digit dna codes which are used to synthesize I am an independent DNA researcher who will shortly prove that he entire validity of the DNA genome as published by Celera (you) and Francis Collins My new DNA Primer Model = Natures Organic Code doesn't consider any of the DNA triangulated codes to "be junk" since over 5 billion years the The current 4 coded dna model forms a square when all the magnetic bonds that is the shape the medicines are taking. The correct dna shapes and structures should be reading the latest dna journals and seeing these dna scientist trying to describe reading the latest dna journals and seeing these dna scientist trying to describe way the dna code has been transcribed into computer based digital data structures which have taken over the "true analysis" from the english dna scientist who of our dna research. We need to stop these people before we digress from the dna to rna to 20 amino acids process... In the chaos and frustration drkyia felt in his 2 organic classes, the most memorable and obvious problem was the data structure of the Watson-crick double helix genetic primer. Drkyia did not know a lot about the chemical reactions of these nucleic acids and amino acids, but he did know tha the coding scheme should be more efficient and symmetrical... We will show how sulfur is the evolutionary thread and string which starts, stops, and controls each and every process step at every level of protein synthesis (i.e. methionine = AUG and Cysteine at the amino acid level, Acetyl Coenzyme A at the glycoprotein fatty acid level, SAM or S-Adenyl-methionine at the hormone or spermidine level, and Tformly met at the tRNA final genetic code instruction set level... The closed benzene Hexagonal heterocyclic ring structure enabled a captured Electron of hydrogen to be trapped in a three dimensional crystalline mirrored tunnel and it is the constant bouncing of the electron which continues to power atomic Quantum Chemical Reactions. Without a closed ring the captured Electron and not make a Full 360 degree Cycle and if is this feedback cycle which allowed learning and experience to develop. The positive and negative feedback loops are in the regulatory mechanisms for all metabolic pathways the never ending synthesis and degradation processes to continue as long as the closed ring the structure is an unbroken and the electron is captured giving electro force to the covalent and Ionic bonds which stabilize the four major class of Human nutrition, namely, Proteins, Carbohydrates, Lipids and it nucleic acids. is it is our firm belief that the genetic code not only in Codes the Blueprints or instruction sets for Amino Asset Proteins but also for Carbohydrates Sugars and Fatty Acid Lipids. It is a of very safe bet that nature and her 4 billion year old
Evolutionary genetic code has no wasted or non functional atomic crystalline structure Lattice Nodes which is what the genetic code truly codes for... the current genetic code was finalized in 1966 some 38 years ago, isn't it about time to update the acquired knowledge which better reflects the scientific facts in 2003? By adding the parent purine nucleotide it inosine to the genetic code, eight amino acids,and 24 Codons will be affected and need to be changed. the amino acids, Alanine, Arginine, Isoleucine, Leucine, proline, Serine, threonine and Valine... There should be an orange purine in the genetic code especially since inosine is Consequences omitting Parent Purine from Genetic Code Conversion of IMP to AMP and GMP, IMP Parent Nucleotide, Belongs Genetic Code Genetic code nucleotides and missing purine parent Genetic code wrong omitted parent purine nucleotide base genetic codes.. Purine Salvage and IMP Parent Purine Nucleotide Omitted in the Current Genetic There should be an orange purine in the genetic code especially since inosine is Consequences omitting Parent Purine from Genetic Code Conversion of IMP to AMP and GMP, IMP Parent Nucleotide, Belongs Genetic Code Genetic code nucleotides and missing purine parent Genetic code wrong omitted parent purine nucleotide base genetic codes.. My "Science of Evolution" for want of a better title traces the path of this 6th organic atomic to people and other animals that ingest this genetic coded synthetic organic molecule? organic molecular structures each doing harm to the evolutionary produced metabolic primer, the blueprint and instruction set for synthesizing the organic components of most basic organic molecular structure is a six sided hexagon, the six positions specifying the X,Y,Z coordinates for symmetrical halves of a "whole" living entity. In organic and number of water molecules made while at the same time producing other organic third major scientific discovery, the identification of the first organic life form to donate "common ancestor" to chromosome 1 in the human genome; the first organic protein or who produce supposedly "therapeutic organic molecules" which can generate revenues of We will demonstrate why every drug, every organic "therapeutic molecule" (i.e... A Symptom Free Therapeutic Organic Molecule Why Does Inosine "Warrant" Inclusion in this most "elite" of Organic Molecules ATP powers over 96% of organic "redox" (oxidationreduction) biochemical reactions The Purines and Pyrmidines were the first organic molecules to have a "closed" not Pauling proposed an orthomolecular approach where one provides organic and not Addition is nature's algorithm for organic life, growth and evolution The male, female and "offspring" "add up" to three organic life forms not two Since this is not how human life or any organic life increases the number in the species, IMP Starter ATP Organic Power Plant Synthesis Process LUCA produces the molecular structure which contains 50% of the organic carbon; this No scientist has ever made a therapeutic or synthetic organic molecule that did and does which make up the genetic primer as well as the metabolic strings between organic atoms the organic association string or linkage continues through the amino acids especially carbohydrates and lipids the two "other" major macromolecular class or
organic synthesized organic medicinal protein is the dosage amounts or catalytic trigger cysteine bonds which are the organic connectors for amino acids to become polypeptides; created a very serious problem in terms of making organic molecules with the right organic aromatic heterocyclic compounds. There would be just long chains of amino frequencies as thermal heat values which "melt" the magnetically bonded organic accumulating the organic mass compounds used in the anabolic ATP process. This evident in all organic living beings. Humans have two hands, two feet, two eyes, two to people and other animals that ingest this genetic coded synthetic organic molecule? organic molecular structures each doing harm to the evolutionary produced metabolic very conservative estimate of the number of therapeutic organic molecules which have If a picture is worth "a thousand words" then visioneering should increase gestalt organic correct structure and formulation for all organic and inorganic compounds. 5 billion year old organic genome, of which, man or homo sapiens is but a small part... sulfphurs SAM purine metabolism and ATP synthesis Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years Will you please state your name for the record. My name is Dr John Allen Berger and I am a scientist who has discovered an some possible fatal flaws with the current genetic code. I believe of the current genetic code is missing one purine nucleotide, but this missing Purine Nucleotide is not just any purine nucleotide it is the parent purine nucleotide it. What what do I mean by the parent? I mean the the first instance of a particular Class of organic molecular structures which the nature has created over the last 4 billion years The nucleotide molecular structure is a very special structure because it is the foundation of the DNA and RNA nucleic acids which archives each and every cells Total Genome, which is a catalog of all the genes or sequences of Purine and Pyrimidine Nucleotides which are the actual Molecular Structures referred to in the genetic code. It is through Purine and Pyrimidine Metabolism that DNA and RNA are formed and produced. The purine molecular structure is of larger than the pyrimidine and
unlike the pyrimidine closed ring the purine ring is never destroyed while Cell is still functioning properly. Rivera The nucleotide molecular structure is a very special structure because it is the foundation of the DNA and RNA nucleic acids which archives each and every cells Total Genome, which is a catalog of all the genes or sequences of Purine and Pyrimidine Nucleotides which are the actual Molecular Structures referred to in the genetic code. It is through Purine and Pyrimidine Metabolism that DNA and RNA are formed and produced. The purine molecular structure is of larger than the pyrimidine and unlike the pyrimidine closed ring the purine ring is never destroyed while Cell is still functioning properly. Rivera The nucleotide molecular structure is a very special structure because it is the foundation of the DNA and RNA nucleic acids which archives each and every cells Total Genome, which is a catalog of all the genes or sequences of Purine and Pyrimidine Nucleotides which are the actual Molecular Structures referred to in the genetic code. It is through Purine and Pyrimidine Metabolism that DNA and RNA are formed and produced. The purine molecular structure is of larger than the pyrimidine and unlike the pyrimidine closed ring the purine ring is never destroyed while Cell is still functioning properly. Rivera The nucleotide molecular structure is a very special structure because it is the foundation of the DNA and RNA nucleic acids which archives each and every cells Total Genome, which is a catalog of all the genes or sequences of Purine and Pyrimidine Nucleotides which are the actual Molecular Structures referred to in the genetic code. It is through Purine and Pyrimidine Metabolism that DNA and RNA are formed and produced. The purine molecular structure is of larger than the pyrimidine and unlike the pyrimidine closed ring the purine ring is never destroyed while Cell is still functioning properly. Rivera We aim to show you that inosine Monophosphate or I M.P. was indeed the first purine nucleotide closed ring of structure created by nature through our natural selection and Inheritance Mechanisms Which Value economy and the efficiency as criteria for survival and hardness and opposed to Extinction because a less costly energy solution which is always a E Molecular Crystalline Structure and and there is always competition between competing at Structures to occupy the role or position which is critical to the survival of the host organism and ecologies of other Chromosomes which adds Symbion Likely developed very efficient communication messaging systems which allow very quick response time to threats or unknown hazards. The prime directive imbedded in each and Cell and each DNA molecule is that survival aholt is greater in any single individual because if the whole host does not survive the nine of the smaller Organizational units such as the Organs Tissues and even cells will not survive. There Leaving the "parent" out of the genetic primer negates the concept of inheritance, does it not? There is a very specific biochemical reason the "omitted parent" nucleotide base was selected or chosen by nature to be the foundation of the purine and pyrmidine molecules which as stated above are the molecules (DNA = A1-T1, G1-C1; RNA = A2-U1, G2-C2) of the genetic primer. Please note the numbering of the genetic codes; as you can see the U1 for T1 substitution is the only difference in the two genetic codes DNA and RNA. This is the critical mistake in the transcription to translation phase of amino acid/peptide/polypeptide/enzyme synthesis...
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Berger code - Wikipedia, the free encyclopedia

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1 information bits). Berger codes can detect any

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Berger code - Wikipedia, the free encyclopedia

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J. M. Berger, "A note on an error detection code for asymmetric channels",

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Inosine Family Inosine and IMP

Inosine Parent Purine

Inosine Mono Phosphate

Adenosine Guanosine Inosine

Inosine Mono Phosphate - first purine "closed ring" hexagonal heterocyclic

ATP Nucleotide TTP Nucleotide

Adenosine Base Thymine Base

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Detailed Summary (berger overview.txt)

Detailed Summary (berger overview.txt)

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