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Table II presents the enzyme activity as well as the... bers of an ordered tetrad.  The strains were grown...
Table II presents the enzyme activity as well as the... bers of an ordered tetrad. The strains were grown...

... only fail to derepress the OCT and LAT enzymes in the presence of 3AT, but showed 50% reduced basal enzyme levels. To further characterize the failure of the mts mutant to regulate amino acid synthetic enzymes in vivo, it was crossed with arg-12^s (a bradytrophic mutation at the structural locus for ...
" Enzymes "
" Enzymes "

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p53 regulation and function in normal cells and tumors
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... genome. p53 is a DNA binding protein; attention has focused on its specific binding to a consensus sequence within promoter regions of growth inhibitory genes. However, p53 also binds sequence-independently to damaged sites in DNA and is postulated to have a role in DNA repair or apoptosis. Mutation ...
Ernest Just - CPO Science
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... AN OFTEN OVERLOOKED FINDING in genetic research is that identical twins can sometimes differ in important ways. For instance, we are often told by TEDS’ parents that their identical twins have very different personalities, likes and dislikes. Because identical twins share 100% of their genes, or DNA ...
Missense mutations in the PAX6 gene in aniridia.
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Missense mutations in the PAX6 gene in aniridia.
Missense mutations in the PAX6 gene in aniridia.

... he Pax gene consists of a family of developmental control genes; nine members have been isolated in vertebrates since paired originally was identified as a segmentation gene in Drosophila melanogaster.1-2 The encoded proteins are transcriptional regulators with DNA binding through a conserved domain ...
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Basic information on pathways
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... THE POLYMERASE CHAIN REACTION (PCR) The PCR reaction is a DNA amplification technique that revolutionized almost all aspects of biological research. The procedure was invented by Dr. Kary Mullis while at Cetus Corporation in 1984. Dr. Mullis was awarded a Nobel Prize for his work in 1994. PCR amplif ...
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... property of the mass‐to‐charge ratio (m/z). This is inherently more accurate than electrophoresis‐based or hybridizationarray‐based methods, which are both susceptible to complications from secondary‐structure formation in nucleic acids. • Furthermore, h the h absolute b l nature off detection, d i ...
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... Conditions for Michaelis -Menten Two assumptions must be met for the MichaelisMenten equation • Steady state - the enzyme substrate complex ES is at a constant value. That is the ES is formed as fast as the enzyme releases the product. For this to happen the concentration of substrate has to be muc ...
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... the right conditions, these bacteria can make authentic human insulin. When allowed to multiply in gigantic vats (fermenters) these bacteria can be used to mass produce the human insulin protein. This genetically engineered insulin is purified using protein chromatography and used to treat patients ...
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Deoxyribozyme



Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of catalyzing specific chemical reactions, similar to the action of other biological enzymes, such as proteins or ribozymes (enzymes composed of RNA).However, in contrast to the abundance of protein enzymes in biological systems and the discovery of biological ribozymes in the 1980s,there are no known naturally occurring deoxyribozymes.Deoxyribozymes should not be confused with DNA aptamers which are oligonucleotides that selectively bind a target ligand, but do not catalyze a subsequent chemical reaction.With the exception of ribozymes, nucleic acid molecules within cells primarily serve as storage of genetic information due to its ability to form complementary base pairs, which allows for high-fidelity copying and transfer of genetic information. In contrast, nucleic acid molecules are more limited in their catalytic ability, in comparison to protein enzymes, to just three types of interactions: hydrogen bonding, pi stacking, and metal-ion coordination. This is due to the limited number of functional groups of the nucleic acid monomers: while proteins are built from up to twenty different amino acids with various functional groups, nucleic acids are built from just four chemically similar nucleobases. In addition, DNA lacks the 2'-hydroxyl group found in RNA which limits the catalytic competency of deoxyribozymes even in comparison to ribozymes.In addition to the inherent inferiority of DNA catalytic activity, the apparent lack of naturally occurring deoxyribozymes may also be due to the primarily double-stranded conformation of DNA in biological systems which would limit its physical flexibility and ability to form tertiary structures, and so would drastically limit the ability of double-stranded DNA to act as a catalyst; though there are a few known instances of biological single-stranded DNA such as multicopy single-stranded DNA (msDNA), certain viral genomes, and the replication fork formed during DNA replication. Further structural differences between DNA and RNA may also play a role in the lack of biological deoxyribozymes, such as the additional methyl group of the DNA base thymidine compared to the RNA base uracil or the tendency of DNA to adopt the B-form helix while RNA tends to adopt the A-form helix. However, it has also been shown that DNA can form structures that RNA cannot, which suggests that, though there are differences in structures that each can form, neither is inherently more or less catalytic due to their possible structural motifs.
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