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The Role of Polymorphic Variants of Gene Components of the PTEN/PI3K/AKT Signaling Pathway in the Development of Prostate Cancer
Gilyazova, I.R., Ivanova, E.A., Bermisheva, M.A., Loginova, M.V., Asadullina, D.D., Ishemgulov, R.R., Mustafin, A.T., Pavlov, V.N., Khusnutdinova, E.K. (2022)
Abstract: The aim of this study was to search for associations of genotypes and alleles
Association of a Single-Nucleotide Variant rs11100494 of the NPY5R Gene with Antipsychotic-Induced Metabolic Disorders
Dobrodeeva, V.S., Shnayder, N.A., Novitsky, M.A., Asadullin, A.R., Vaiman, E.E., Petrova, M.M., Limankin, O.V., Neznanov, N.G., Garganeeva, N.P., Nasyrova, R.F. (2022)
-time PCR to study the carriage of major and minor alleles of the SNV rs11100494 (1164C>A) of the NPY5R gene
ВЛИЯНИЕ ПОЛИМОРФИЗМА ГЕНА G1082AIL-10 НА ТЕЧЕНИЕ ОСТРЫХ КИШЕЧНЫХ ИНФЕКЦИЙ
INFLUENCE OF G1082A IL-10 GENE POLYMORPHISM ON THE COURSE OF ACUTE INTESTINAL INFECTIONS
Епифанцева, Н.В., Витковский, Ю.А., Epifantseva, N.V., Vitkovsky, Yu.A. (2022)
Excel 2010, Statistica 6.0. Results. In all the subjects, the predominance of the dominant allele G
Correlations of Gene Variants LEP rs2167270, LEPR rs1137100, GHRL rs696217, rs27647, and NPY rs16147 with Obesity and Adolescent Eating Behavior: Case-Control Study
Kochetova, O. V., Shangareeva, Z.A., Viktorova, T.V., Korytina, G.F., Viktorov, V.V., Кочетова, О.В., Шангареева, З.А., Викторова, Т.В., Корытина, Г.Ф., Викторов, В.В. (2022)
pathological allele
АССОЦИАЦИЯ ВАРИАНТОВ ГЕНОВ LEP RS2167270, LEPR RS1137100, GHRL RS696217, RS27647 И NPY RS16147 С ОЖИРЕНИЕМ И ПИЩЕВЫМ ПОВЕДЕНИЕМ ПОДРОСТКОВ: ИССЛЕДОВАНИЕ "СЛУЧАЙ-КОНТРОЛЬ"
Кочетова, О.В., Шангареева, З.А., Викторова, Т.В., Корытина, Г.Ф., Викторов, В.В., Kochetova, O.V., Shangareeva, Z.A., Viktorova, T. V., Korytina, G.F., Viktorov, V.V. (2022)
PATHOLOGICAL ALLELE
ОСОБЕННОСТИ ПОЛИМОРФИЗМА ГЕНОВ РЕНИН-АНГИОТЕНЗИНОВОЙ СИСТЕМЫ У НЕДОНОШЕННЫХ НОВОРОЖДЕННЫХ
FEATURES OF GENE POLYMORPHISM OF THE RENIN-ANGIOTENSIN SYSTEM IN PREMATURE NEWBORNS
Миронов, П.И., Амирова, В.Р., Грешилов, А.А., Потехина, Т.А., Рахимова, Р.Ф., Mironov, P.I., Amirova, V.R., Greshilov, A.A., Potekhina, T.A., Rahimova, P.F. (2022)
The role of retroelements in the development of hereditary tumor syndromes
Mustafin, R.N., Khusnutdinova, E.K., Мустафин, Р.Н., Хуснутдинова, Э.К. (2022)
Predicting the risk of congenital cleft lip and palate during pregnancy planning in patients residing in a polluted region using genetic markers
Chuykin, O.S., Viktorova, T.V., Gil'manov, M.V., Kochetova, O.V., Kuchuk, K.N., Чуйкин, О.С., Викторова, Т.В., Гильманов, М.В., Кочетова, О.В., Кучук, К.Н. (2022)
Multilocus evaluation of genetic predictors of multiple sclerosis
Timasheva, Y, Nasibullin, TR, Tuktarova, IA, Erdman, VV, Galiullin, TR, Zaplakhova, OV, Bakhtiiarova, KZ (2022)
histocompatibility region. Multilocus analysis has revealed 322 and 27 allelic patterns associated with multiple
Exosomal miRNA-146a is downregulated in clear cell renal cell carcinoma patients with severe immune-related adverse events
Ivanova, E., Asadullina, D., Rakhimov, R., Izmailov, A., Izmailov, Al., Gilyazova, G., Galimov, Sh., Pavlov, V., Khusnutdinova, E., Gilyazova, I. (2022)
in the miRNA-146a gene demonstrated that CC genotype and C allele carriers had higher risk of developing

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