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and proopiomelanocortin receptors. We studied the association of the single-nucleotide variants (SNVs) rs11100494 and rs

healthy donors (62.56±14.05). 10 single nucleotide polymorphisms (SNPs) were genotyped by the real

of these dependencies with ADHD. DNA was collected and six polymorphic loci of genes of the dopaminergic

РОЛЬ ГЕНОВ МИКРОРНК УЧАСТНИКОВ VHL-HIF1α ПУТИ В РАЗВИТИИ СВЕТЛОКЛЕТОЧНОГО РАКА ПОЧКИ

single-locus and multilocus approach to identify genetic predictors of T1D. Results We found that LTA rs

ASSOCIATIONS OF COMMON VARIANTS AT 1P11.2 AND 14Q24.1 (RAD51L1) WITH BREAST CANCER RISK AND HETEROGENEITY BY TUMOR SUBTYPE: FINDINGS FROM THE BREAST CANCER ASSOCIATION CONSORTIUMA genome-wide association study (GWAS) identified single-nucleotide polymorphisms (SNPs) at 1p11

ПОИСК ИЗМЕНЕНИЙ НУКЛЕОТИДНОЙ ПОСЛЕДОВАТЕЛЬНОСТИ ГЕНА РЕМОДЕЛИРОВАНИЯ ХРОМАТИНА PBRM1 У ПАЦИЕНТОВ СО СВЕТЛОКЛЕТОЧНЫМ РАКОМ ПОЧКИ of ccRCC. The aim of our investigation is identification of changes in the nucleotide sequence

in oncogenesis. Germline DNA samples from cervical cancer patients were analyzed in order to identify nucleotide

Роль полиморфного локуса VNTR гена аггрекана в развитии остеоартроза у женщин of the aggrecan gene (ACAN) VNTR polymorphism, which is represented by a variable number of 57 nucleotide repeats

Роль молекулярно-генетических изменений структуры гена CDH1 в развитии рака желудка у пациентов из Республики Башкортостанsearch for changes in nucleotide sequence

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