Sentence examples for several nucleotide polymorphisms from inspiring English sources

Exact(6)

Here, we show that a wild-derived mouse strain MOLF/EiJ expresses high levels of colonic epithelial CHI3L1 at the steady state due to several nucleotide polymorphisms in the proximal promoter regions of the CHI3L1 gene.

Several nucleotide polymorphisms in Rtcl, Rth3, Rum1, and Rul1 were significantly (P < 0.05) associated with seedling root traits in maize suggesting that all four tested genes are involved in the maize root development.

Several nucleotide polymorphisms were observed in the amplified portion of the NCCR of the New Haven WUPyV serum isolates.

Several nucleotide polymorphisms including two nonsynonymous mutations were found in the coding region of γ-TMT3 between Ichihime and KAS, but none of which was responsible for the difference in α-tocopherol concentration.

Sequence comparisons of the three genes between ALHF and aabys revealed several nucleotide polymorphisms in the coding regions of CYP4D4v2 and CYP4G2, while no nucleotide polymorphisms were identified in the coding region of CYP6A38.

Comparison of the deduced protein sequences of CYP4D4v2, CYP4G2, and CYP6A38 between ALHF and aabys revealed identical protein sequences, although several nucleotide polymorphisms were found in the coding regions of these three genes between the two strains (Figs. 2, 3, 4).

Similar(54)

VEGF is encoded by the VEGF gene [ 13], which is polymorphic, with several single nucleotide polymorphisms (SNPs) in regulatory regions [ 14].

The potential value of haplotypes defined by several single nucleotide polymorphisms has attracted recent interest.

Recent genome-wide association (GWA) studies identified several single nucleotide polymorphisms (SNPs) predisposing to colorectal cancer (CRC).

Comparison of patients with coronary heart disease and controls in genome-wide association studies has revealed several single nucleotide polymorphisms (SNPs) associated with coronary heart disease.

Several single nucleotide polymorphisms (SNP) near IL28B gene (encoding IFN-λ3), including SNP rs12979860, were shown to be linked with SVR [1 3].

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