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Полигенный анализ полногеномных маркеров рассеянного склероза
Genome-wide polygenic analysis of multiple sclerosis markers
Timasheva, Y.R., Nasibullin, T.R., Tuktarova, I.A., Erdman, V.V., Galiullin, T.R., Zaplakhova, O.V., Bakhtiiarova, K.Z., Тимашева, Я.Р., Насибуллин, Т.Р., Туктарова, И.А., Эрдман, В.В., Галиуллин, Т.Р., Заплахова, О.В., Бахтиярова, К. (2021)
in the ethnic groups of Bashkirs, Russians, and Tatars living in the Republic of Bashkortostan (Russian
Prevalence of age-related macular degeneration and retinal pseudodrusen in an elderly population. The ural very old study
Bikbov, Mukharram M., Kazakbaeva, Gyulli M., Iakupova, Ellina M., Fakhretdinova, Albina A., Gilmanshin, Timur R., Panda-Jonas, Songhomitra, Jonas, Jost B. (2025)
.8, 2.5) persons respectively. Conclusions: In this ethnically mixed, very old population, AMD
ПРОБЛЕМА ОЖИРЕНИЯ У МОЛОДЫХ ЖЕНЩИН
OBESITY IN YOUNG WOMEN
Галиханова, Л.И., Ямлихина, Э. Г., Муталова, Э.Г., Galikhanova, L.I., Yamlikhina, E.G., Mutalova, E.G. (2020)
Клинический и молекулярно-генетический анализ случая семейного рассеянного склероза
CLINICAL AND MOLECULAR GENETIC ANALYSIS OF A CASE OF FAMILIAL MULTIPLE SCLEROSIS IN THE REPUBLIC OF BASHKORTOSTAN
ЗАПЛАХОВА, О.В., ТИМАШЕВА, Я.Р., БАХТИЯРОВА, К.З., ТУКТАРОВА, И.А., МУСТАФИНА, О.Е., TIMASHEVA Y.R., ZAPLAKHOVA O.V., BAKHTIYAROVA K.Z., TUKTAROVA I.A., MUSTAFINA O.E. (2019)
ЯЗЫК ГОРОДА КАК СОЦИОЛИНГВИСТИЧЕСКАЯ ПРОБЛЕМА: ПЕРСПЕКТИВЫ ИЗУЧЕНИЯ
CITY LANGUAGE AS A SOCIOLINGUISTIC PROBLEM: STUDY PROSPECTS
ИСМАГИЛОВА, Н.В., МАЙОРОВА, О.А., Ismagilova, N.V., Mayorova, O.A. (2019)
The Study of Association of Polymorphic Markers of the SOD1, SOD2, and SOD3 Genes with Longevity
Erdman, V.V., Nasibullin, T.R., Tuktarova, I.A., Timasheva, Y.R., Danilko, K.V., Viktorova, T.V., Mustafina, O.E. (2020)
(rs1799895). We detected ethnicity-specific patterns of the distribution of genotype frequencies
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
of Tatar ethnicity with a high frequency. In the general cohort of unrelated patients from
CLINICAL AND EPIDEMIOLOGICAL CHARACTERISTICS OF HEREDITARY MOTOR-SENSORY NEUROPATHY 1X CAUSED BY THE MUTATION C. 259C> G (P. P87A) IN THE GJB1 GENE OF PATIENTS FROM THE REPUBLIC OF BASHKORTOSTAN
Saifullina, E.V., Magzhanov, R.V., Khidiyatova, I.M., Khusnutdinova, E.K. (2017)
of Bashkortostan.To study in details the territorial ethnic distribution and clinical manifestations of the с.259C
AVPR1A MAIN EFFECT AND OXTR-BY-ENVIRONMENT INTERPLAY IN INDIVIDUAL DIFFERENCES IN DEPRESSION LEVEL
KAZANTSEVA, A.V., DAVYDOVA, YU.D., ENIKEEVA, R.F., LOBASKOVA, M.M., MUSTAFIN, R.N., MALYKH, S.B., TAKHIROVA, Z.R., KHUSNUTDINOVA, E.K. (2020)
models (PLINK v.1.9) adjusted for multiple comparisons. Results: We observed ethnicity-specific main
ASSOCIATION OF GENES INVOLVED IN NICOTINE AND TOBACCO SMOKE TOXICANT METABOLISM (CHRNA3/5, CYP2A6, AND NQO1) AND DNA REPAIR (XRCC1, XRCC3, XPC, AND XPA) WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
Korytina, G.F., Akhmadishina, L.Z., Kochetova, O.V., Burduk, Yu.V., Aznabaeva, Yu.G., Zagidullin, Sh.Z., Victorova, T.V. (2014)
for association with the development and progression of chronic obstructive pulmonary disease (COPD) in ethnic

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