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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
PADI4 GENE POLYMORPHISM AS A PREDICTOR OF RESPONSE TO METHOTREXATE IN PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS
Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2016)
of the study was to assess whether the PADI4 rs2240336 gene polymorphism is a predictor of the disease severity
Association of the ACTN3 Gene’s Single-Nucleotide Variant Rs1815739 (R577X) with Sports Qualification and Competitive Distance in Caucasian Athletes of the Southern Urals
Balberova, Olga V., Shnayder, Natalia A., Bykov, Evgeny V., Zakaryukin, Yuri E., Petrova, Marina M., Soloveva, Irina A., Narodova, Ekaterina A., Chumakova, Galina A., Al-Zamil, Mustafa, Asadullin, Azat R., Vaiman, Elena E., Trefilova, Vera V., Nasyrova, Regina F. (2023)
gene with qualification and competitive distance in Caucasian athletes of the Southern Urals. Methods
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)
Barashkov, Nikolay A., Pshennikova, Vera G., Posukh, Olga L., Teryutin, Fedor M., Solovyev, Aisen V., Klarov, Leonid A., Romanov, Georgii P., Gotovtsev, Nyurgun N., Kozhevnikov, Andrey A., Kirillina, Elena V., Sidorova, Oksana G., Vasilyevа, Lena M., Fedotova, Elvira E., Morozov, Igor V., Bondar, Alexander A., Solovyevа, Natalya A., Kononova, Sardana K., Rafailov, Adyum M., Sazonov, Nikolay N., Alekseev, Anatoliy N., Tomsky, Mikhail I., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Fedorova, Sardana A. (2016)
Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause
Perspective for Studying the Relationship of miRNAs with Transposable Elements
Mustafin, R.N., Khusnutdinova, E. (2023)
Transposable elements are important sources of miRNA, long non-coding RNAs genes, and their targets
Взаимосвязь между полиморфизмами генов хемокинов и хемокиновых рецепторов и восприимчивостью к хронической обструктивной болезни легких у татарского населения из России: исследование случай-контроль
The Relationship Between Chemokine and Chemokine Receptor Genes Polymorphisms and Chronic Obstructive Pulmonary Disease Susceptibility in Tatar Population from Russia: A Case Control Study
Korytina, G.F., Aznabaeva, Y.G., Akhmadishina, L.Z., Kochetova, O.V., Nasibullin, T.R., Zagidullin, N.S., Zagidullin, S.Z., Viktorova, T.V., Коритина, Г. Ф., Азнабаева, Ю. Г., Ахмадишина, Л. З., Кочетова, О.В., Насибуллин, Т.Р., Загидуллин, Н. Ш., Загидуллин, Ш.З., Викторова, Т.В. (2022)
The Relationship Between Chemokine and Chemokine Receptor Genes Polymorphisms and Chronic
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
in more than 70 genetic loci. The main causes of HSP development are mutations in the SPAST gene
AVPR1A MAIN EFFECT AND OXTR-BY-ENVIRONMENT INTERPLAY IN INDIVIDUAL DIFFERENCES IN DEPRESSION LEVEL
KAZANTSEVA, A.V., DAVYDOVA, YU.D., ENIKEEVA, R.F., LOBASKOVA, M.M., MUSTAFIN, R.N., MALYKH, S.B., TAKHIROVA, Z.R., KHUSNUTDINOVA, E.K. (2020)
Background: Multiple studies of depression indicated a significant role of gene
MOLECULAR AND BIOCHEMICAL STUDY OF GLUTARIC ACIDURIA TYPE 1 IN 49 RUSSIAN FAMILIES: NINE NOVEL MUTATIONS IN THE GCDH GENE
KURKINA, M.V., MIHAYLOVA, S.V., BAIDAKOVA, G.V., SAIFULLINA, E.V., KOROSTELEV, S.A., PYANKOV, D.V., KANIVETS, I.V., YUNIN, M.A., PECHATNIKOVA, N.L., ZAKHAROVA, E.YU (2020)
) (ICD-10 code: E72.3; MIM 231670) is an autosomal recessive disease caused by mutations in the gene

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