Examples of using A polymorphism in English and their translations into Portuguese
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Colloquial
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Official
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Medicine
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Financial
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Ecclesiastic
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Ecclesiastic
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Computer
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Official/political
The variables studied included serum pon1 activity, a polymorphism in the promoter region of the gene c(-107)
A polymorphism consists of a 30 bp VNTR located above the 1.2kb coding sequences of MAO-A MAO-Au VNTR
Furthermore, the- 93 g>a polymorphism in the mlh1 gene have been associated with increased risk of developing colorectal cancer by the fact of being located in the promoter region of the gene.
by Yi et al., the presence of a polymorphism in the PAX2 gene a gene which is involved in renal maturation was not associated with the occurrence of HSP, but did increase genetic susceptibility to nephritis.
The clinical presentation shows a polymorphism and the severity scope of the signals
to determine the frequency of a polymorphism is also difficult.
when associated with a polymorphism of the mineralocorticoid receptor gene,
healthy Americans, and narcoleptics with cataplexy have identified the existence of a polymorphism in the T-cell receptor alpha TRAgene.
Recently, six novel polymorphisms have been described for the IL-13 locus including a polymorphism in exon 4 +2044G/A leading to an amino acid substitution at position 130 Arg130Gln,
youth depressive episodes was moderated by a polymorphism in the promoter region of the serotonin transporter gene(5-httlpr),
A polymorphism in the cox2 promoter gene(g-765c rs20417)
studies that have evaluated the impact of a polymorphism of the MAOA gene demonstrated that genetic influence on behavior is only seen in the presence of abuse at infancy.
which could mean that the 1359 G/A polymorphism would not be related to vulnerability for this disorder,
the A allele of the -308 G/A polymorphism Chi2 7.09,
it is linked to the presence of a polymorphism in the promoter of the serotonin transporter gene,
Thus, the goal of the present paper was to identify the T-> A polymorphism, which results in the substitution of aminoacid Leucine leu for Isoleucine ile in position 306 of the protein from gene TAX1BP1 in patients with head
The aim of this study was to evaluate the genotypic and allele frequencies of the apoe gene and blmh 1450 g>a polymorphism and blmh expression through,
KIR3DL1/KIR3DS1 interact with HLA-Bw4 that differs from Bw6, because of a polymorphism in positions 77 and 80.
However, it has been reported by different authors as a polymorphism, a causative recessive
However, V27I mutation was previously reported to be a polymorphism without pathological effects and unrelated to hearing loss.