По вашему запросу найдено документов: 86

Страница 1 из 9

Ассоциация полиморфных вариантов генов (HTR2A, MTNR1A, MTNR1B, CLOCK, DRD2) и бессонницы при синдроме зависимости от алкоголя
Association of polymorphic variants of genes (HTR2A, MTNR1A, MTNR1B, CLOCK, DRD2) and insomnia in alcohol dependence syndrome
Efremov, I.S., Asadullin, A.R., Dobrodeeva, V.S., Shnayder, N.A., Akhmetova, E.A., Tukhvatullina, D.R., Krupitsky, E.M., Nasyrova, R.F., Ефремов, И.С., Асадуллин, А.Р., Добродеева, В.С., Шнайдер, Н.А., Ахметова, Э.А., Тухватуллина, Д.Р., Крупицкий, Е.М., Насырова, Р.Ф. (2021)
Association of polymorphic variants of genes (HTR2A, MTNR1A, MTNR1B, CLOCK, DRD2) and insomnia
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Baxter, J.S., Johnson, N., Tomczyk, K, Gillespie, A., Maguire, S., Brough, R., Fachal, L, Michailidou, K., Bolla, M.K., Wang, Q., Dennis, J., Ahearn, T.U., Bermisheva, M. (2021)
(signal 1), 5 (signal 2), and 42 (signal 3) credible causal variants at these loci. We used publicly
Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Park, H.A., Neumeyer, S., Michailidou, K., Bolla, M.K., Wang, Q., Dennis, J., Ahearn, T.U., Andrulis, I.L., Anton-Culver, H., Antonenkova, N.N., Arndt, V., Aronson, K.J, Bermisheva, M., other authors (2021)
single-nucleotide polymorphisms (SNPs) reported in genome-wide association studies of lifetime smoking
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers
Johnson, N., Maguire, S., Morra, A., Kapoor, P.M., Tomczyk, K., Jones, M.E., Schoemaker, M.J., Gilham, C., Bolla, M.K., Wang, Q., Bermisheva, M. (2021)
in the aetiology of breast cancer. The aim of this analysis was to identify genetic variants that are associated
Потенциал использования микроРНК в судебно-медицинской экспертизе
The potential use of miRNAs in forensic science
Gareev, I.F., Beylerli, O.A., Izmailov, A.A., Гареев, И.Ф., Бейлерли, О.А., Измайлов, А.А. (2021)
The level of secondary messengers and the redox state of NAD+/NADH are associated with sperm quality in infertility
Galimov, S.N., Gromenko, J.Y., Bulygin, K.V., Galimov, K.S., Galimova, E.F., Sinelnikov, M.Y. (2021)
In order to explore the interrelation of Calcium, cAMP, and redox state of pyridine nucleotides
Familial environment modifies association of DNA methyltransferases gene variants and cognitive functioning
Enikeeva, R, Kazantseva, A, Takhirova, Z, Lobaskova, M, Davydova, Y, Mustafin, R, Malykh, S, Khusnutdinova, E (2021)
Familial environment modifies association of DNA methyltransferases gene variants and cognitive
Breast cancer risk genes - Association analysis in more than 113,000 women
Dorling, L., Carvalho, S., Allen, J., González-Neira, A., Luccarini, C., Wahlström, C., Pooley, K.A., Parsons, M.T., Fortuno, C., Wang, Q., Bolla, M.K., Dennis, J., Bermisheva, M., Khusnutdinova, E., Prokofyeva, D., other additional authors (2021)
. In separate analyses for protein-truncating variants and rare missense variants in these genes, we estimated
Ассоциации молекулярно-генетических предикторов сахарного диабета 2-го типа с гипергликемией у новорожденных с экстремально низкой массой тела
Associations of molecular genetic predictors of type 2 diabetes mellitus with hyperglycemia in extremely low birth weight infants
Mironov, P.I., Mingazov, N.N., Valiev, R.R., Lekmanov A.U., МИРОНОВ, П. И., МИНГАЗОВ, Н. Н., ВАЛИЕВ, Р. Р., ЛЕКМАНОВ, А. У. (2021)
Investigating the role of osteoprotegerin gene polymorphic variants in osteoporosis
Yalaev, B.I., Tyurin, A.V., Mirgalieva, R.I., Khusnutdinova, E.K., Khusainova, R.I. (2021)
- Polymorphic variants rs3134069, rs3102734, rs7844539 and rs3102734 are potential markers of the risk

Страница 1 из 9

Google Scholar
OpenDoar

Фасеты

Авторы
Ключевые слова
Год