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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
Novel Genetic Risk Marker for Paranoid Schizophrenia in the Chromosomal Region 9q21.13 in Tatars: A Genome-Wide Association Analysis
Gareeva, A.E. (2024)
with paranoid schizophrenia and 383 healthy individuals of Tatar ethnicity. As a result of the study
СИНДРОМ МЮНХМЕЙЕРА: ГЕНЕТИЧЕСКИЕ МЕХАНИЗМЫ, ТЕХНОЛОГИИ ДИАГНОСТИКИ И ЛЕЧЕНИЯ
MUNCHMEYER SYNDROME: GENETIC MECHANISMS, DIAGNOSTIC AND TREATMENT TECHNOLOGIES
Батыршин, А. А., Batyrshin, A.A. (2024)
THE ROLE OF THE POLYMORPHISM rs28362491 OF THE NFKB1 GENE IN THE GASTRIC CANCER DEVELOPMENT
Nurgalieva, A.Kh., Mustafin, S.A., Petrova, S.G., Ekomasova, N.V., Sakaeva, D.D., Fedorova, Y.Y., Abdeeva, G.R., Dzhaubermezov, M.A., Abdeev, R.R., Rakhimov, R.R., Khusnutdinova, E.K., Prokofyeva, D.S. (2024)
. The samples for the study were the DNA of 374 patients with GC and 365 healthy donors of various ethnicities
Searching for Ethnospecific Risk Markers of Paranoid Schizophrenia in Bashkirs Based on the Results from Genome-Wide Association Study
Gareeva, A.E. (2024)
ethnicity
Genome-Wide Analysis of the Risk Association for the Development of Paranoid Schizophrenia in Russians: Search for Genetic Markers in the 1q43 Chromosomal Region
Gareeva, A.E. (2024)
ethnicity
ПРЕДИКТОРЫ ОККЛЮЗИОННЫХ НАРУШЕНИЙ ПО ДАННЫМ ТЕЛЕРЕНТГЕНОГРАФИИ
PREDICTORS OF OCCLUSIVE DISORDERS ACCORDING TO TELERENTGENOGRAPHY
ДЕВЯТИРИКОВ, Д.А., ПУТАЛОВА, И.Н., СУСЛО, А.П., СЛАВНОВ, А.А., ШИРОЧЕНКО, С.Н., ГРИНЕНКО, О.В., СИДЕНКО, Н.И., Devyatirikov, D.A., Putalova, I.N., Suslo, A.P., Slavnov, A.A., Shirochenko, S.N., Grinenko, O.V., Sidenko, N.I. (2024)
ДИАГНОСТИЧЕСКОЕ ЗНАЧЕНИЕ МОЛЕКУЛ АДГЕЗИИ ICAM-1 и VCAM-1 В ПАТОГЕНЕЗЕ РАССЕЯННОГО СКЛЕРОЗА
THE DIAGNOSTIC VALUE OF ADHESIVE MOLECULES ICAM-1 AND VCAM-1 IN THE PATHOGENESIS OF MULTIPLE SCLEROSIS
Ващенко, В.И., Туктарова, И.А., Насибуллин, Т.Р., Тимашева, Я.Р., Vashchenko, V.I., Tuktarova, I.A., Nasibullin, T.R., Timasheva, Y.R. (2024)
The Genetic Markers of Knee Osteoarthritis in Women from Russia
Tyurin, Anton, Akhiiarova, Karina, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)
to the clinical and ethnic heterogeneity of the studied populations. To find the genetic markers
Hypomethylation of the RUNX2 Gene Is a New Potential Biomarker of Primary Osteoporosis in Men and Women
Yalaev, Bulat, Tyurin, Anton, Akhiiarova, Karina, Khusainova, Rita (2024)
years of age of Russian ethnicity from the Volga-Ural region of Russia was carried out. The level of DNA

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