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Searching for Ethnospecific Risk Markers of Paranoid Schizophrenia in Bashkirs Based on the Results from Genome-Wide Association Study
Gareeva, A.E. (2024)
Abstract: It is now known that schizophrenia is a multifactorial disease in which both genetic
Association of Polymorphic Loci of Long Noncoding RNA Genes (H19, MEG3, MALAT1, LINC00305, LINC00261, LINC02227, and CDKN2B-AS1) with Chronic Obstructive Pulmonary Disease
Korytina, G.F., Akhmadishina, L.Z., Markelov, V.A., Nasibullin, T.R., Aznabaeva, Y.G., Kochetova, O.V., Khusnutdinova, N.N., Larkina, A.P., Zagidullin, N. Sh., Victorova, T.V. (2024)
is to identify the association between polymorphic variants of H19 (rs3741219), MEG3 (rs7158663), MALAT1 (rs
Исследование роли полиморфных вариантов генов MTHFR и MTRR в развитии желчнокаменной болезни
The role of MTHFR and MTRR gene polymorphisms in the development of cholelithiasis
Fedorova, Yu.Yu., Nurgalieva, A.Kh., Petrova, S.G., Murzina, R.R., Dzhaubermezov, M.A., Ekomasova, N.V., Khusnutdinova, E.K., Prokofieva, D.S., Федорова, Ю. Ю., Нургалиева, А. Х., Петрова, С. Г., Мурзина, Р. Р., Джаубермезов, М. А., Екомасова, Н. В., Хуснутдинова, Э. К., Прокофьева, Д. С. (2024)
The role of MTHFR and MTRR gene polymorphisms in the development of cholelithiasis
Germline Variants in Proto-Oncogenes and Tumor Suppressor Genes in Women with Cervical Cancer
Lenkova, Ksenia, Khusainova, Rita, Minyazeva, Raushaniya, Zaripova, Aliya, Gilyazova, Irina, Mokrysheva, Natalia, Minniakhmetov, Ildar (2024)
, characterized by genetic heterogeneity and a complex molecular landscape, both of which contribute to its
MicroRNA binding site variants–new potential markers of primary osteoporosis in men and women
Yalaev, Bulat, Deev, Roman, Tyurin, Anton, Salakhov, Ramil, Smirnov, Kirill, Eremkina, Anna, Mokrysheva, Natalia, Minniakhmetov, Ildar, Khusainova, Rita (2024)
with microRNAs. Methods: The authors searched for associations of polymorphic variants of microRNA binding
Relationship of Retroelements with Antiviral Proteins and Epigenetic Factors in Alzheimer's Disease
Mustafin, Rustam Nailevich (2024)
Genetic factors such as allelic variants of the PSEN1, PSEN2, APP, and APOE genes play an important
ВЛИЯНИЕ ПОЛИМОРФИЗМОВ ГЕНОВ MTHFR, MTRR, MTR ОБМЕНА ФОЛИЕВОЙ КИСЛОТЫ И ВИТАМИНА В12 НА НЕВЫНАШИВАНИЕ БЕРЕМЕННОСТИ
THE EFFECT OF POLYMORPHISMS OF THE GENES MTHFR, MTRR, MTR OF FOLIC ACID AND VITAMIN B12 METABOLISM ON MISCARRIAGE
Макаров, Е.О., Makarov, E.O. (2024)
THE EFFECT OF POLYMORPHISMS OF THE GENES MTHFR, MTRR, MTR OF FOLIC ACID AND VITAMIN B12 METABOLISM
РОЛЬ МОЛЕКУЛЯРНОЙ ГЕНЕТИКИ В МЕДИЦИНЕ
THE ROLE OF MOLECULAR GENETICS IN MEDICINE
Шадиева, К.И., Сайфуллина, А.В., Хамидуллина, А.Р., Shadieva, K.I., Saifullina, A.V., Khamidullina, A.R. (2024)
THE ROLE OF MOLECULAR GENETICS IN MEDICINE
Population Characteristics of the Spectrum and Frequencies of CFTR Gene Mutations in Patients with Cystic Fibrosis from the Republic of Bashkortostan (Russia)
Ayupova, Guzel, Litvinov, Sergey, Akhmetova, Vita, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)
regulator gene (CFTR) mutations in the population, which is determined by genetic diversity and ethnicity
СИНДРОМ МЮНХМЕЙЕРА: ГЕНЕТИЧЕСКИЕ МЕХАНИЗМЫ, ТЕХНОЛОГИИ ДИАГНОСТИКИ И ЛЕЧЕНИЯ
MUNCHMEYER SYNDROME: GENETIC MECHANISMS, DIAGNOSTIC AND TREATMENT TECHNOLOGIES
Батыршин, А. А., Batyrshin, A.A. (2024)
MUNCHMEYER SYNDROME: GENETIC MECHANISMS, DIAGNOSTIC AND TREATMENT TECHNOLOGIES

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