Sentence examples for influence of variant from inspiring English sources

As such, studies which have found up to a 40% variation in warfarin dose could be explained by the influence of variant CYP2C9 and VKORC1 SNPs in the respective study populations [ 53, 54].

The influence of variants morphology and the material property to constitutive behavior is considered.

Our results are consistent with an influence of variants in the CHRNA5 CHRNA3 CHRNB4 gene cluster on cognitive measures.

At these positions, we further required that the derived alleles have frequencies between 5 and 15% in the human populations to minimize the influence of variants potentially under positive selection or balancing selection.

We investigated the influence of variants in the genes encoding neuron-restrictive silencer factor (NRSF) and brain-derived neurotrophic factor (BDNF), proteins previously associated with cognition and epilepsy, on cognitive function in people with newly diagnosed epilepsy.

Very few studies have investigated the influence of variants in these nine genes on HCV infection [ 10, 18].

We aim to investigate the influence of variants and associated methylation in the GSTM gene cluster with changes in lung function growth during adolescence.

Further studies of the influence of variants of the UCP1 gene on AIRg in other populations, and investigations of the interplay between UCP1 and UCP2 on glucose-stimulated insulin secretion, are warranted.

The influence of variants at the 9p21 locus on melanoma risk has been reported through investigation of CDKN2A variants through candidate gene approach as well as by genome wide association studies (GWAS).

Previously we presented the influence of variants in TPH2 on depression measurement scores during the pregnancy [ 47] and that of variants in the serotonin transporter 5-HTTLPR on different depression levels after childbirth with regard to lifetime and current psychological stressors [ 50].

The determination of individual haplotypes is valuable in many areas of research, including (i) association studies and disease risk, where the analysis of haplotypes is more powerful than the analysis of single markers alone [ 4] and where there may be a haplotype-dependent influence of variants on risk [ 5, 6], (ii) evolution and population genetics [ 7- 9] and (iii) pharmacogenomics [ 10].