Sentence examples for variant in subject from inspiring English sources

Taking into account only conclusive shapes, the combined results of the gag and env highlighter plots suggest transmission of a single viral variant in subject PO, and transmission of multiple viral variants in subjects A, D, OJ, and QP.

We define an indicator variable Iij which takes values of zero, one or two according to the number of mutant alleles of variant i in subject j.

Third, we review our identification and functional characterization of multiple, hyperactive SERT coding variants in subjects with autism.

SI variants were found in over 45% of BM variants in Subjects 7, 10, and 16, while 100% of the BM and PL sequences were predicted to be SI in Subject 33.

The reason for this discrepancy is unclear but one possible explanation is that the latter study measured selection pressure by measuring the frequency of variants in optimal epitopes in subjects with the presenting allele compared with subjects lacking the presenting allele arguing that a high frequency of variants in subjects without the presenting allele was evidence of a low fitness cost.

We also detected additional rare and possibly damaging GNB1L sequence variants in subjects with ASD.

We evaluated the occurrence of CTRC variants in subjects with RAP, CP, and controls from the North American Pancreatitis Study II cohort.

It is also worth emphasizing that we set out to identify KLHL3 and CUL3 variants in subjects with a clinical diagnosis of FHHt on the basis of measurements routinely recorded in the clinic.

Although K8 R341H variant may predispose to development of end-stage liver failure, the limited numbers of patients available as well as the low frequency of keratin variants within the cohort make it impossible for this study to conclusively clarify the significance of keratin variants in subjects with alcohol-related liver cirrhosis.

Coupled with observations of other investigators for its involvement in schizophrenia, our detection of a translocation disrupting GNB1L and potentially damaging, extremely rare GNB1L variants in subjects with autism provides evidence that this gene may have a role in the pathogenesis of autism and expands the number of phenotypes associated with GNB1L.

However, the dominant W680G variant in this subject almost completely disappeared three years later, suggesting that whatever pressure selected for this variant was transitory in nature.