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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 allergic airway tract diseases in children. © Pleiades Publishing, Inc. 2024. ISSN 1022-7954, Russian
OPINIONS OF HEARING PARENTS ABOUT THE CAUSES OF HEARING IMPAIRMENT OF THEIR CHILDREN WITH BIALLELIC GJB2 MUTATIONS
Solovyev, A.V., Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Bady-Khoo, M.S., Lobov, S.L., Popova, N.Y., Romanov, G.P., Sazonov, N.N., Bondar, A.A., Morozov, I.V., Tomsky, M.I., Fedorova, S.A., Khusnutdinova, E.K. (2017)
Abstract Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent
Analysis of association between histamine receptor gene HRH1, HRH2, HRH3, HRH4 polymorphisms and asthma in children
Savelieva, O.N., Karunas, , A.S., Fedorova, Yu.Yu., Gatiyatullin, R.F., Etkina, E.I., Khusnutdinova, E.K., Савельева, О. Н., Карунас, А. С., Федорова, Ю. Ю., Гатиятуллин, Р. Ф., Эткина, Э. И., Хуснутдинова, Э. К. (2021)
and asthma in children
РОЛЬ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНОВ АРГИНАЗ (ARG1, ARG2), УЧАСТВУЮЩИХ В МЕТАБОЛИЗМЕ БЕТА-2-АГОНИСТОВ, В РАЗВИТИИ И ТЕЧЕНИИ БРОНХИАЛЬНОЙ АСТМЫ
THE ROLE OF POLYMORPHIC VARIANTS OF ARGINASE GENES (ARG1, ARG2) INVOLVED IN BETA-2-AGONIST METABOLISM IN THE DEVELOPMENT AND COURSE OF ASTHMA
САВЕЛЬЕВА, О.Н., КАРУНАС, А.С., ФЕДОРОВА, Ю.Ю., МУРЗИНА, Р.Р., САВЕЛЬЕВА, А.Н., ГАТИЯТУЛЛИН, Р.Ф., ЭТКИНА, Э.И., ХУСНУТДИНОВА, Э.К., SAVELIEVA O.N., KARUNAS A.S., FEDOROVA YU.YU., MURZINA R.R., SAVELIEVA A.N., GATIYATULLIN R.F., ETKINA E.I., KHUSNUTDINOVA E.K. (2020)
EPIGENETIC MARKERS OF ASTHMA: A STUDY OF METHYLATION PATTERNS OF GENES INVOLVED IN DRUG METABOLISM
Savelieva, O.N., Karunas, A.S., Vlasova, A.O., Ahmetshin, A.A., Khidiyatova, I.M., Khusnutdinova, E.K. (2024)
Asthma is a common chronic multifactorial respiratory disease. Genes involved in the metabolism
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)
The c.-23+1G>A splice site mutation is one of the most frequent mutations of gene GJB2 (Cx26, 13q11
COVID-19, Retroelements, and Aging
Mustafin, R.N., Khusnutdinova, E.K. (2021)
infections, and changes in the L1 retrotransposon expression patterns in the lung tissues of COVID-19
ANALYSIS OF CLINICAL MANIFESTATIONS OF NEUROFIBROMATOSIS TYPE 1 IN PATIENTS WITH NONSENSE PATHOGENIC VARIANTS IN THE NF1 GENE FROM THE REPUBLIC OF BASHKORTOSTAN
Mustafin, R.N., Bermisheva, M.A., Karunas, A.S., Akhmetshin, A.A., Monakhova, A.S., Khusnutdinova, E.K. (2025)
frequently. Of the 23 nonsense pathogenic variants we identified, 16 pathogenic variants were previously
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
FEDOROVA, Y.Y., KARUNAS, A.S., GIMALOVA, G.F., KHUSNUTDINOVA, E.K., SAVELIEVA, O.N, MURZINA, R.R., GATIYATULLIN, R.F., ETKINA, E.I. (2019)
with the rs37973 AG and rs37973 GG genotypes of the GLCCI1 gene compared with children with rs37973 AA
Нейрофиброматоз 1‑го типа: результаты собственного исследования (Республика Башкортостан)
Neurofibromatosis type 1: Results of our own study (Republic of Bashkortostan)
Mustafin, R.N., Bermisheva, M.A., Valiev, R.R., Khusnutdinova, E.K., Мустафин, Р. Н., Бермишева, М. А., Валиев, Р. Р., Хуснутдинова, Э. К. (2021)

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