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По вашему запросу найдено документов: 545

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Skeletal anomalies in patients with neurofibromatosis type 1

Mustafin, R.N. (2022)

», «treatment», «frequency», «prevalence», «genotype-phenotype correlation», « modifier genes». Results

Роль полиморфных вариантов нескольких генов матриксных металлопротеиназ и их тканевых ингибиторов в развитии рака желудка

The Role of Polymorphic Variants of Several Genes of Matrix Metalloproteinases and Their Tissue Inhibitors in the Development of Gastric Cancer

growth. The genes of matrix metalloproteinases and their inhibitors, as well as many other genes

FORECASTING MODEL OF GENE ENZYME POLYMORPHISM DETOXIFICATION IN PATIENTS SUFFERED FROM HFRS

Hasanova, G.M. / Хасанова Г.М., Valishin, D.A. / Валишин Д.А, Tutel'jan, A.V. / Тутельян А.В., Hasanova, A.N. / Хасанова А.Н. (2016)

Aim: to study gene enzyme polymorphism of xenobiotic detoxification in patients suffered from HFRS

Single-Nucleotide Polymorphisms as Biomarkers of Antipsychotic-Induced Akathisia: Systematic Review

Nasyrova, Regina F, Vaiman, Elena E, Repkina, Vera V, Khasanova, Aiperi K, Asadullin, Azat R, Shipulin, German A, Altynbekov, Kuanysh S, Al-Zamil, Mustafa, Petrova, Marina M, Shnayder, Natalia A (2023)

IA) from the DRD2 gene as well as the TT genotype rs13212041 (77461407 C>T) from the HTR1B gene were found

Breast cancer risk genes - Association analysis in more than 113,000 women

Dorling, L., Carvalho, S., Allen, J., González-Neira, A., Luccarini, C., Wahlström, C., Pooley, K.A., Parsons, M.T., Fortuno, C., Wang, Q., Bolla, M.K., Dennis, J., Bermisheva, M., Khusnutdinova, E., Prokofyeva, D., other additional authors (2021)

BACKGROUND Genetic testing for breast cancer susceptibility is widely used, but for many genes

ИССЛЕДОВАНИЕ РОЛИ ПОЛИМОРФНОГО ВАРИАНТА ГЕНА АМИНОКСИДАЗЫ 1 (AOC1) В РАЗВИТИИ И ТЕЧЕНИИ БРОНХИАЛЬНОЙ АСТМЫ

THE ROLE OF AMINOXIDASE 1 (AOC1) GENE POLYMORPHISM IN THE DEVELOPMENT AND COURSE OF ASTHMA

Федорова, Ю.Ю., Савельева, О.Н., Карунас, А.С., Мурзина, Р.Р., Актаева, Е.Е., Гатиятуллин, Р.Ф., Эткина, Э.И., Хуснутдинова, Э.К., Yu.Yu. Fedorova, O.N. Savelieva, A.S. Karunas, R.R. Murzina, E.E. Aktaeva, R.F. Gatijatullin, E.I. Еtkina, E.K. Khusnutdinova (2020)

THE ROLE OF AMINOXIDASE 1 (AOC1) GENE POLYMORPHISM IN THE DEVELOPMENT AND COURSE OF ASTHMA

АНАЛИЗ ВЗАИМОДЕЙСТВИЯ АЛЛЕЛЕЙ ГЕНА-РЕЦЕПТОРА ВИТАМИНА D ПРИ МИОПИИ

ANALYSIS OF THE INTERACTION OF THE VITAMIN D RECEPTOR GENE ALLELES IN MYOPIA

ГОРБУНОВА, В.Ю., РЕЗБАЕВА, Г.Н., ВОРОБЬЕВА, Е.В., ГАЛИМОВА, В.У., GORBUNOVA, V.YU., REZBAEVA, G.N., VOROBYEVA, E.V., GALIMOVA, V.U. (2021)

ANALYSIS OF THE INTERACTION OF THE VITAMIN D RECEPTOR GENE ALLELES IN MYOPIA

HEARING LOSS OF VOLGA-URAL REGION IN RUSSIA

Khusnutdinova, E.K., Dzhemileva, L.U., Lobov, S.L., Kuznetzov, D.U., Nazirova, A.G., Nurgalina, E.M., Barashkov, N.A., Fedorova, S.A. (2017)

carrier frequency of c.35delG, c.167delT and c.235delC mutations of the GJB2 gene in 17 populations

ГЕНЕТИЧЕСКИЕ МАРКЕРЫ ОСТЕОАРТРИТА У ЖЕНЩИН С НЕДИФФЕРЕНЦИРОВАННОЙ ДИСПЛАЗИЕЙ СОЕДИНИТЕЛЬНОЙ ТКАНИ

SEARCH FOR OSTEOARTHRITIS GENETIC MARKERS IN WOMEN WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA

Khusainova, R.I., Tyurin, A.V., Shapovalova, D.A., Khusnutdinova, E.K., Хусаинова Р.И., Тюрин А.В., Шаповалова Д.А., Хуснутдинова Э.К. (2017)

We conducted an association study of ten polymorphisms in six candidate genes of OA (rs1799750 (MMP

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)

Polymorphisms of the CHRNA5/A3, CYP2A6, NQO1, XPC, XRCC1, CRCC3, XPD, and XPA genes were tested

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