Sentences with phrase «c polymorphisms»

Similar results were observed for the rs3750952 G > C polymorphism.

Not exact matches

Zhu F, Dollé ME, Berton TR, Kuiper RV, Capps C, Espejo A, McArthur MJ, Bedford MT, van Steeg H, de Vries A, Johnson DG (2010) Mouse models for the p53 R72P polymorphism mimic human phenotypes.

«The IL - 28B first came to the attention of virologists when it was shown that polymorphisms, small genetic changes, in this gene were associated with different hepatitis C virus treatment outcomes.

This section invites manuscripts describing (a) Linkage, association, substitution or positional mapping and epigenetic studies in any species; (b) Validation studies of candidate genes using genetically - engineered mutant model organisms; (c) Studies focused on epistatis and gene - environment interactions; (d) Analysis of the functional implications of genomic sequence variation and aim to attach physiological or pharmacogenomic relevance to alterations in genes or proteins; (e) Studies of DNA copy number variants, non-coding RNA, genome deletions, insertions, duplications and other single nucleotide polymorphisms and their relevance to physiology or pharmacology in humans or model organisms, in vitro or in vivo; and (f) Theoretical approaches to analysis of sequence variation.

Interestingly, the three most common SNP variants detected in the LNCaP and 22Rv1 - associated XMRV genomes, the aforementioned A → G polymorphism at position 790, an A → G polymorphism at position 4264 and a C → G polymorphism at position 8112, can also be found in the VP35, VP42, and VP62 XMRV genomes, with the exception that the C → G polymorphism is not observed in VP35 due to lack of sequence coverage.

The DRD2 polymorphisms were scored by two independent observers, where the T - probe signal corresponded to the TaqIA - 1 allele and the C - probe signal corresponded to the TaqIA - 2 allele.

We describe a common, functional C > T single nucleotide polymorphism, rs25532, located less than 150 nucleotides centromeric of the serotonin transporter - linked polymorphic region indel known as 5 - HTTLPR.

Polymorphisms in the CRP gene moderate an association between depressive symptoms and circulating levels of C - reactive protein