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2254298, rs2228485, rs13316193) gene polymorphisms together with haplotypic and G × E effects

, on the basis of the analysis of variability of nine SNP markers, five different haplotypes in deaf patients

loci and the TNFA rs1800629*G - LTA rs909253*G haplotype are associated with the development of JIA

РОЛЬ ПОЛИМОРФНЫХ ЛОКУСОВ ГЕНА РЕЦЕПТОРА ОКСИТОЦИНА (OXTR) В РАЗВИТИИ АГРЕССИВНОГО ПОВЕДЕНИЯ У ЗДОРОВЫХ ИНДИВИДОВHAPLOTYPE

ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ ПОПУЛЯЦИИ, ПРОЖИВАЮЩЕЙ НА ТЕРРИТОРИИ РЕСПУБЛИКИ БАШКОРТОСТАН
Логинова, М.А., Парамонов, И.В., В.Н. Павлов, Сафуанова, Г.Ш., Loginova, M.A., Paramonov, I.V., Pavlov, V.N., Safuanova, G.Sh. (Вестник трансплантологии и искусственных органов, 2016)
.84%), 04 (11.61%). 711 HLA-A-B-C-DRB1 four-locus haplotypes were determined using the software Arlequin v.3

and 114 unaffected unrelated individuals without this variant were used for a haplotype analysis based

), NFKB1 rs28362491 (in girls) and the haplotype TNFA rs1800629*A-LTA rs909253*G (in girls). Conclusion

). Logistic regression was used to detect the association of SNPs and haplotypes of linked loci in different

-hip ratio (WHR, p=0.007), body mass index (BMI, p=0.039). The participants having the C-C haplotype of CRP

study is aimed to estimate both the genetic- and haplotype-based effects of the OXTR and AVPR1B genes

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