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ПОПУЛЯЦИОННО-ГЕНЕТИЧЕСКОЕ ИССЛЕДОВАНИЕ РАСПРЕДЕЛЕНИЯ И НАСЛЕДОВАНИЯ АЛЛЕЛЕЙ ГЕНА НЕЙРОПИЛИН-1 (NRP1) В БАШКОРТОСТАНЕ
POPULATION GENETIC STUDY OF THE DISTRIBUTION AND INHERITANCE OF NEUROPILIN-1 (NRP1) GENE ALLELES IN BASHKORTOSTAN
Бушман, Я.Р., Данилко, К.В., Bushman, Y.R., Danilko, K.V. (2024)
POPULATION GENETIC STUDY OF THE DISTRIBUTION AND INHERITANCE OF NEUROPILIN-1 (NRP1) GENE ALLELES
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
A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)
in certain populations by specific genetic background and population structure. At least, the data from
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene
Barashkov, N.A., Konovalov, F.A., Borisova, T.V., Teryutin, F.M., Solovyev, A.V., Pshennikova, V.G., Sapojnikova, N.V., Vychuzhina, L.S., Romanov, G.P., Gotovtsev, N.N., Morozov, I.V., Bondar, A.A., Platonov, F.A., Burtseva, T.E., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A. (2021)
the genetic cause of congenital cataract spread in this population, we performed whole-exome sequencing
Genetic Polymorphisms of Cytochromes P450 in Finno-Permic Populations of Russia
Dzhaubermezov, M., Ekomasova, N., Mustafin, R., Gabidullina, L., Galimova, Y., Nurgalieva, A., Valova, Y., Prokofyeva, D., Khusnutdinova, E. (2022)
individuals of 5 Finno-Permic populations from the territories of the European part of the Russian Federation
РОЛЬ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНА ОСТЕОПРОТЕГЕРИНА, РЕЦЕПТОРА ВИТАМИНА D И САЙТОВ СВЯЗЫВАНИЯ МИКРОРНК В РАЗВИТИИ ОСТЕОПОРОЗА
THE ROLE OF POLYMORPHIC VARIANTS OF THE OSTEOPROTEGERIN GENE, VITAMIN D RECEPTOR, AND MICRORNA BINDING SITES IN THE DEVELOPMENT OF OSTEOPOROSIS
Ялаев, Б.И., Тюрин, А.В., Нурлыгаянов, Р.З., Хусаинова, Р.И., Yalaev, B.I., Tyurin, A.V., Nurlygayanov, R.Z., Khusainova, R.I. (2020)
of their contribution to the structure of OP pathogenesis is relevant [1-2]. The development of OP depends on genetic
ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ СИНДРОМА ДЕФИЦИТА ВНИМАНИЯ/ГИПЕРАКТИВНОСТИ. СОВРЕМЕННОЕ СОСТОЯНИЕ ПРОБЛЕМЫ
GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS OF THE PROBLEM
Р. Р. Шарафиев, R. R. Sharafiev, А. Р. Асадуллин, A. R. Asadullin, В. Л. Юлдашев, V. L. Yuldashev, А. В. Анцыборов, A. V. Antsyborov, Л. В. Лямина, L. V. Lyamina, Э. А. Ахметова, E. A. Akhmetova (Медицинский вестник Башкортостана, №4, 2018)
GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS
RECONSTRUCTION OF SNP HAPLOTYPES WITH MUTATION C.-23+1G>A IN HUMAN GENE GJB2 (CHROMOSOME 13) IN SOME POPULATIONS OF EURASIA
Solovyev, A.V., Barashkov, N.A., Bady-Khoo, M.S., Zytsar, M.V., Posukh, O.L., Romanov, G.P., Rafailov, A.M., Sazonov, N.N., Alexeev, A.N., Dzhemileva, L.U., Khusnutdinova, E.K., Fedorova, S.A. (2017)
homozygous for mutation c.-23+1G>A from six Eurasian populations were reconstructed. The structure
MULTILOCUS ASSOCIATIONS OF INFLAMMATORY GENES WITH THE RISK OF TYPE 1 DIABETES
TIMASHEVA, Y.R., NASIBULLIN, T.R., MUSTAFINA, O.E., BALKHIYAROVA, Z.R., PROKOPENKO, I., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
Background Genome-wide association studies have captured a large proportion of genetic variation
ПРОБЛЕМЫ И ДОСТИЖЕНИЯ В ИЗУЧЕНИИ КЛИНИКО-ГЕНЕТИЧЕСКИХ АСПЕКТОВ МУКОВИСЦИДОЗА
PROBLEMS AND ACHIEVEMENTS IN THE STUDY OF CLINICAL AND GENETIC ASPECTS OF CYSTIC FIBROSIS
АЮПОВА, Г.Р., МИННИАХМЕТОВ, И.Р., ХУСАИНОВА, Р.И., AYUPOVA, G.R., MINNIAKHMETOV, I.R., KHUSAINOVA, R.I. (2022)
PROBLEMS AND ACHIEVEMENTS IN THE STUDY OF CLINICAL AND GENETIC ASPECTS OF CYSTIC FIBROSIS

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