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По вашему запросу найдено документов: 96

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GENETIC ASPECTS OF KERATOCONUS DEVELOPMENT

Bikbova, M.M., Usubova, E.L., Oganisyana, K.Kh., Lobov, S.L., Khasanovad, R.R., Dzhemilevab, L.U., Khusnutdinova, E.K. (2017)

to individual populations and to certain ethnic groups in general.

THE ROLE OF OXYTOCIN RECEPTOR (OXTR) GENE POLYMORPHISMS IN THE DEVELOPMENT OF AGGRESSIVE BEHAVIOR IN HEALTHY INDIVIDUALS

DAVYDOVA, YU. D., KAZANTSEVA, A. V., ENIKEEVA, R. F., MUSTAFIN, R.N., ENIKEEVA, R. F., LOBASKOVA, M. M., MALYKH, S. B., GILYAZOVA, I.R., KHUSNUTDINOVA, E.K. (2020)

on individual differences in aggression level in 623 mentally healthy individuals with sex and ethnicity

ASSOCIATIONS OF POLYMORPHIC DNA MARKERS AND THEIR COMBINATIONS WITH MULTIPLE SCLEROSIS

Zaplakhova, O. V., Nasibullin, T. R., Tuktarova, I. A., Timasheva, Y. R., Erdman, V. V., Bakhtiyarova, K. Z., Mustafina, O. E. (2018)

. Both samples were formed from the ethnic group of Russians. The results of the investigation

Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases

Savelieva, O.N., Karunas, A.S., Biktasheva, A.R., Vlasova, A.O., Khidiyatova, I.M., Etkina, E.I., Khusnutdinova, E.K. (2024)

of Bashkortostan. DNA samples of 358 individuals with allergic airway diseases of different ethnicity (Russians—165

Evaluation of Polygenic Risk Score for Prediction of Childhood Onset and Severity of Asthma

Savelieva, Olga, Karunas, Alexandra, Prokopenko, Inga, Balkhiyarova, Zhanna, Gilyazova, Irina, Khidiyatova, Irina, Khusnutdinova, Elza (2025)

, were used. The study group was comprised of Russian, Tatar, Bashkir, and mixed ethnicity individuals

The frequent variant A57F in the GNE gene in patients from Russia has Finno-Ugric Mari origin

Subbotin, Dmitrii, Ionova, Sofya, Marakhonov, Andrey, Saifullina, Elena, Borovikov, Artem, Akhmadeeva, Leila, Chausova, Polina, Ryzhkova, Oksana, Zinchenko, Rena, Kutsev, Sergey, Murtazina, Aysylu (2024)

_170delinsTT (p.(Ala57Phe)) variant in the GNE gene (NM_001128227.3) among different ethnic populations (Mari

Анализ ассоциаций с рассеянным склерозом генетических маркеров предрасположенности, выявленных в результате полногеномных исследований

The analysis of association between multiple sclerosis and genetic markers identified in genome-wide association studies

ТИМАШЕВА, Я.Р., НАСИБУЛЛИН, Т.Р., ТУКТАРОВА, И.А., ЭРДМАН, В.В., ГАЛИУЛЛИН, Т.Р., ЗАПЛАХОВА, О.В., БАХТИЯРОВА, К.З., МУСТАФИНА, О.Е., TIMASHEVA, Y.R., NASIBULLIN, T.R., TUKTAROVA, I.A., ERDMAN, V.V., GALIULLIN, T.R., ZAPLAKHOVA, O.V., BAKHTIIAROVA, K.Z., MUSTAFINA, O.E. (2020)

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

Myopic Macular Atrophy in the Two-Continent Population-Based Study

Jonas, Jost B., Bikbov, Mukharram M., Kazakbaeva, Gyulli M., Wang, Ya Xing, Xu, Jie, Jonas, Rahul A., Panda-Jonas, Songhomitra (2024)

) and myopic patchy atrophies (MMD stage 3) in three ethnically different cohorts recruited in a population

SPECTRUM AND FREQUENCY OF THE GJB2 GENE PATHOGENIC VARIANTS IN A LARGE COHORT OF PATIENTS WITH HEARING IMPAIRMENT LIVING IN A SUBARCTIC REGION OF RUSSIA (THE SAKHA REPUBLIC)

and allelic frequencies of the GJB2 gene vary significantly among different ethnic groups worldwide. Until now

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