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Mutational mechanisms

Changes in transporter proteins by high-frequency genetic mutation mechanisms, while maintaining transport activity, helps to evade the host s immune response, and in cases where the substrate specificity is changed, helps the microorganism to adapt to new iron sources. [Pg.117]

Ohta T, Gray TA, Rogan PK et al. Imprinting-mutation mechanisms in Prader-Willi syndrome. Am ) Hum Genet 1999 64[2] 397-413. [Pg.36]

Pech, M., Hochtl, J., Schnel], H., Zachau, H.G. (1981). Differences between germ-line and rearranged immunoglobulin VK coding sequences suggest a localized mutation mechanism. Nature 291, 668-670. [Pg.85]

Roy CN, Andrews NC. Recent advances in disorders of iron metabolism mutations, mechanisms and modifiers. Hum Molec Genet 2001 10 2181-6. [Pg.1532]

Fig. 3A Role of exogenous and endogenous factors in shaping tumor mutation patterns. Mini-hotspots in the p53 coding sequence. Distribution of four mutation types in the coding sequence, GC to AT transitions at CpG (representing 23% of all mutations), GC to TA transversions (15%), GC to CG (8%), and AT to GC (12%). CpG transitions primarily appear as the consequence of an endogenous mutation mechanism and form well-defined mutation hotspots. Because of these major hotspots, the mini-hotspots corresponding to other mutation types are difficult to detect. Only sites that contain more than 1 % of a specific mutation type are shown. Hotspot codons for each mutation type are indicated. Some of the non-CpG hotspots are well-characterized sites of alteration induced by exogenous carcinogens (see Fig. 5). Fig. 3A Role of exogenous and endogenous factors in shaping tumor mutation patterns. Mini-hotspots in the p53 coding sequence. Distribution of four mutation types in the coding sequence, GC to AT transitions at CpG (representing 23% of all mutations), GC to TA transversions (15%), GC to CG (8%), and AT to GC (12%). CpG transitions primarily appear as the consequence of an endogenous mutation mechanism and form well-defined mutation hotspots. Because of these major hotspots, the mini-hotspots corresponding to other mutation types are difficult to detect. Only sites that contain more than 1 % of a specific mutation type are shown. Hotspot codons for each mutation type are indicated. Some of the non-CpG hotspots are well-characterized sites of alteration induced by exogenous carcinogens (see Fig. 5).
Expansion of trinucleotide repeat sequences is the mutational mechanism in at least 16 neurological disorders,... [Pg.461]

Lewis W, Levine ES, Griniuviene B, Tankersley KO, Colacino JM, Sommadossi JP, Watanabe KA, Perrino FW (1996b) Fialiuidine and its metabolites inhibit DNA polymerase y at sites of multiple adjacent analog incorporation, decrease mtDNA abundance, and cause mitochraidrial structural defects in cultiued hepatoblasts. Proc Natl Acad Sd USA 93 3592-3597 Lewis W, Copeland WC, Day BJ (2001) Mitochondrial DNA depletion, oxidative stress and mutation mechanisms of dysfunction from nucleoside reverse transcriptase inhihitors. Lab Invest 81 777-790... [Pg.358]

Ma Shangquan, et al. 2000. Application Research on Rheoloy and Mutation Mechanism in Coal and Gas Outbursts, Jiangsu Coal, 3 13-15. [Pg.961]

R. A. Cairns, and T. W. Mak, Oncogenic isocitrate dehydrogenase mutations mechanisms, models, and clinical opportunities. Cancer Discov., 3 (2013) 730-41. [Pg.25]

Once the new generation of chromosomes has been formed, a mutation mechanism comes into operation in the chromosomes, a number of genes are modified in a completely arbitrary manner. Typically, however, this modification concerns only one gene to a thousand, so... [Pg.303]

However, if cells pretreated as above were inoculated into a medium without antibiotics, colonies of the rodlike cells reappeared, reversing into the original, non-induced state. Therefore, P. freudenreichii strain El behaved as a natural mutant. No mutagenesis was used to induce this strain, and the high yield of spherical forms excluded completely the involvement of mutational mechanisms. [Pg.53]


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See also in sourсe #XX -- [ Pg.187 , Pg.188 , Pg.189 ]




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