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REPLICATIVE STUDY OF GWAS-ASSOCIATED CANDIDATE GENE LOCI IN PATIENTS WITH OSTEOARTHRITIS FROM THE BASHKORTOSTAN REPUBLIC
TYURIN, A.V., SHAPOVALOVA, DARIA, DAVLETSHIN, RASHIT, KHUSAINOVA, RITA, LUKMANOVA, L.Z. (2019)
the pathophysiology of OA is given to the identification of genetic and epigenetic mechanisms.
IN SEARCH FOR GENETIC MARKERS OF NON-FAMILIA SICK SINUS SYNDROME
Zagidullin, N., Plechev, V., Badykova, E., Badykov, M., Akhmadishina, L., Korytina, G., Sagitov, I. (2019)
dozen genetic loci are under investigations. Objective To investigate whether 5 connective tissue and 5
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)
and LTA rs909253 genetic variant. LTA rs909253 and TNF rs1800629 loci were also featured in combinations
Pembrolizumab monotherapy for the adjuvant treatment of renal cell carcinoma post-nephrectomy: Randomized, double-blind, Phase III KEYNOTE-564 study
Timasheva, Yu., Zudina, L., Balkhiyarova, Zh., Kaakinen, M., Munroe, P., Prokopenko, I. (2019)
pathophysiological mechanisms. Large-scale genome-wide association studies (GWAS) have revealed hundreds of genetic
GENOME-WIDE ASSOCIATION AND TRANSCRIPTOME STUDIES IDENTIFY TARGET GENES AND RISK LOCI FOR BREAST CANCER
Ferreira, M.A., Gamazon, E.R., Al-Ejeh, F., Aittomäki, K., Andrulis, I.L., Anton-Culver, H., Arason, A., Arndt, V., Aronson, K.J., Arun, B.K., Asseryanis, E., Azzollini, J., Balmaña, J., Barnes, D.R., Barrowdale, D., Beckmann, M.W., Behrens, S., Benitez, J., Bermisheva, M., Białkowska, K., Blomqvist, C., Bogdanova, N.V., Bojesen, S.E., Bolla, M.K., Borg, A., Brauch, H., Brenner, H., Broeks, A., Burwinkel, B., Caldés, T., Caligo, M.A., Campa, D., Campbell, I., Canzian, F., Carter, J., Carter, B.D., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Christiansen, H., Chung, W.K., Claes, K.B.M., Clarke, C.L., Adlard, J., Ahmed, M., Barwell, J., Henderson, A., Hodgson, S., Izatt, L., Kennedy, M.J., Lalloo, F., Miller, C., Morrison, P.J., Ong, K.-R., Perkins, J., Porteous, M.E., Rogers, M.T., Side, L.E., Snape, K., Walker, L., Harrington, P.A., Arnold, N., Auber, B., Bogdanova-Markov, N., Borde, J., Caliebe, A., Ditsch, N., Dworniczak, B., Engert, S., Faust, U. (2019)
loci. Here we hypothesize that some risk-associated variants might act in non-breast tissues
МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ АНАЛИЗ СЛУЧАЯ ЧАСТИЧНОЙ ДЕЛЕЦИИ Y-ХРОМОСОМЫ В СУДЕБНО-МЕДИЦИНСКОЙ ПРАКТИКЕ
MOLECULAR-GENETIC ANALYSIS OF A RARE FORENSIC CASE OF PARTIAL DELETION OF THE Y-CHROMOSOME
ТИМАШЕВА, Я.Р., ТУКТАРОВА, И.А., ГИЗУЛЛИНА, Л.И., СУНДЫРЕВ, Е.Ю., МУСТАФИНА, О.Е., Timasheva Ya.R., Tuktarova I.A., Gizullina L.I., Sundyrev E.Yu., Mustafina O.E. (2019)
MOLECULAR-GENETIC ANALYSIS OF A RARE FORENSIC CASE OF PARTIAL DELETION OF THE Y-CHROMOSOME
ЭПИГЕНЕТИКА АГРЕССИВНОГО ПОВЕДЕНИЯ
EPIGENETICS OF AGGRESSIVE BEHAVIOR
MUSTAFIN, R.N., KHUSNUTDINOVA, E.K., KAZANTSEVA, A.V., ENIKEEVA, R.F., DAVYDOVA, Y.D., KARUNAS, A.S., MALYKH, S.B., МУСТАФИН Р. Н., КАЗАНЦЕВА А.В., ЕНИКЕЕВА Р.Ф., ДАВЫДОВА Ю.Д., КАРУНАС А.С., МАЛЫХ С.Б., ХУСНУТДИНОВА Э.К. (2019)
owing to the impaired interaction with noncoding RNAs, which results in modified functioning of genetic
АССОЦИАЦИЯ АЛЛЕЛЬНЫХ ВАРИАНТОВ ГЕНОВ IL2, IL2RA И IL7R С РАССЕЯННЫМ СКЛЕРОЗОМ
ASSOCIATION BETWEEN ALLELIC VARIANTS OF IL2, IL2RA, AND IL7R GENES AND MULTIPLE SCLEROSIS
TIMASHEVA, Y.R., ZAPLAKHOVA, O.V., NASIBULLIN, T.R., TUKTAROVA, I.A., ERDMAN, V.V., MUSTAFINA, O.E., BAKHTIIAROVA, K.Z., ТИМАШЕВА Я.Р., ЗАПЛАХОВА О.В., НАСИБУЛЛИН Т.Р., ТУКТАРОВА И.А., ЭРДМАН В.В., БАХТИЯРОВА К., МУСТАФИНА О.Е. (2019)
of genetic and environmental factors leading to the development of a complex of autoimmune
THE ROLE OF THE IMMUNE RESPONSE MEDIATOR GENES POLYMORPHISM IN THE PREDISPOSITION TO JUVENILE IDIOPATHIC ARTHRITIS
NAZAROVA, L.S., DANILKO, K.V., MALIEVSKY, V.A., BAKIROV, A.B., VIKTOROVA, T.V. (2019)
loci and the TNFA rs1800629*G - LTA rs909253*G haplotype are associated with the development of JIA
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

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