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ЭФФЕКТИВНОСТЬ ЛЕЧЕНИЯ ТУБЕРКУЛЕЗА С ШИРОКОЙ ЛЕКАРСТВЕННОЙ УСТОЙЧИВОСТЬЮ У ПАЦИЕНТОВ С РАЗНЫМ ГЕНОТИПОМ ПО ГЕНАМ ФЕРМЕНТОВ БИОТРАНСФОРМАЦИИ CYP2В6 И NAT2

EFFICACY OF TREATMENT OF EXTENSIVE DRUG RESISTANT TUBERCULOSIS IN PATIENTS WITH DIFFERENT GENOTYPES IN THE BIOTRANSFORMATION ENZYME GENES OF CYP2B6 AND NAT2

ЮНУСБАЕВА, М.М., БОРОДИНА, Л.Я.., БИЛАЛОВ, Ф.С., ШАРИПОВ, Р.А., НАСИБУЛЛИН, Т.Р., ЮНУСБАЕВ, Б.Б., YUNUSBAEVA, M.M., BORODINA, L. YA., BILALOV, F.S., SHARIPOV, R.A., NASIBULLIN, T.R., YUNUSBAEV, B.B. (2020)

SINGLE NUCLEOTIDE POLYMORPHISM

THE ASSOCIATION OF THE PTPN22 RS2476601 GENE POLYMORPHISM WITH JUVENILE IDIOPATHIC ARTHRITIS IN CHILDREN FROM RUSSIA

Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2017)

factors [1]. The protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene single-nucleotide

СПОСОБ ПРОГНОЗИРОВАНИЯ ИДИОПАТИЧЕСКОГО МУЖСКОГО БЕСПЛОДИЯ НА ОСНОВЕ АНАЛИЗА НУКЛЕОТИДНЫХ ВАРИАНТОВ В ГЕНЕ МИТОХОНДРИАЛЬНОГО ЦИТОХРОМА В

METHOD OF PREDICTION OF IDIOPATHIC MALE INFERTILITY BASED ON ANALYSIS OF NUCLEOTIDE VARIANTS IN MITOCHONDRIAL CYTOCHROME B GENE

METHOD OF PREDICTION OF IDIOPATHIC MALE INFERTILITY BASED ON ANALYSIS OF NUCLEOTIDE VARIANTS

ПОИСК ИЗМЕНЕНИЙ НУКЛЕОТИДНОЙ ПОСЛЕДОВАТЕЛЬНОСТИ ГЕНА РЕМОДЕЛИРОВАНИЯ ХРОМАТИНА PBRM1 У ПАЦИЕНТОВ СО СВЕТЛОКЛЕТОЧНЫМ РАКОМ ПОЧКИ

IDENTIFICATION OF ALTERATIONS IN THE NUCLEOTIDE SEQUENCE OF THE CHROMATIN REMODELING GENE PBRM1 IN CLEAR CELL RENAL CELL CARCINOMA PATIENTS

Klimentova E.A., Gilyazova I.R., Izmailov A.A., Sultanov I.M., Bermisheva M.A., V.N. Pavlov, Khusnutdinova E.K., КЛИМЕНТОВА, Е.А., ГИЛЯЗОВА, И.Р., ИЗМАЙЛОВ, А.А., СУЛТАНОВ, И.М., БЕРМИШЕВА, М.А., В.Н. Павлов, ХУСНУТДИНОВА, Э.К. (2018)

of ccRCC. The aim of our investigation is identification of changes in the nucleotide sequence

РОЛЬ ГЕНОВ МИКРОРНК УЧАСТНИКОВ VHL-HIF1α ПУТИ В РАЗВИТИИ СВЕТЛОКЛЕТОЧНОГО РАКА ПОЧКИ

THE ROLE OF MIRNA GENES PARTICIPATING IN VHL-HIF1α IN CLEAR CELL RENAL CELL CARCINOMA

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

Baxter, J.S., Johnson, N., Tomczyk, K, Gillespie, A., Maguire, S., Brough, R., Fachal, L, Michailidou, K., Bolla, M.K., Wang, Q., Dennis, J., Ahearn, T.U., Bermisheva, M. (2021)

(signal 1), 5 (signal 2), and 42 (signal 3) credible causal variants at these loci. We used publicly

Searching for Ethnospecific Risk Markers of Paranoid Schizophrenia in Bashkirs Based on the Results from Genome-Wide Association Study

Gareeva, A.E. (2024)

610000 single nucleotide polymorphisms (SNPs). © Pleiades Publishing, Inc. 2024. ISSN 1022-7954, Russian

Role of Retroelements in Frontotemporal Dementia Development

Mustafin, Rustam Nailevich (2025)

to trigger FTD by activating specific retroelements. FTD is associated with multiple single nucleotide

IREB2, CHRNA5, CHRNA3, FAM13A & HEDGEHOG INTERACTING PROTEIN GENES POLYMORPHISMS & RISK OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE IN TATAR POPULATION FROM RUSSIA

Korytina, G.F., Akhmadishina, L.Z., Viktorova, E.V., Kochetova, O.V., Viktorova, T.V. (2016)

and hedgehog interacting protein (HHIP) genes in a Tatar population from Russia. Methods: Six single

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

Park, H.A., Neumeyer, S., Michailidou, K., Bolla, M.K., Wang, Q., Dennis, J., Ahearn, T.U., Andrulis, I.L., Anton-Culver, H., Antonenkova, N.N., Arndt, V., Aronson, K.J, Bermisheva, M., other authors (2021)

single-nucleotide polymorphisms (SNPs) reported in genome-wide association studies of lifetime smoking

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