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ИССЛЕДОВАНИЯ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНОВ В МЕДИЦИНЕ ТРУДА
STUDIES ON POLYMORPHIC GENES VARIANTS IN OCCUPATIONAL HEALTH
КУДОЯРОВ, Э.Р., КАРИМОВ, Д.О., БАКИРОВ, А.Б., KUDOYAROV, E.R., KARIMOV, D.O., BAKIROV, A.B. (2020)
GENOME-WIDE ASSOCIATIVE STUDY
FINE-MAPPING OF 150 BREAST CANCER RISK REGIONS IDENTIFIES 191 LIKELY TARGET GENES
FACHAL, L., KAR, S., TYRER, J.P., GHOUSSAINI, M., HARRINGTON, P.A., HEALEY, C.S., MAYES, R., SHAH, M., PHAROAH, P.D.P., EASTON, D.F., DUNNING, A.M., ASCHARD, H., JIANG, X., TAMIMI, R.M., KHUSNUTDINOVA, E., BIAŁKOWSKA, K., и др. соавторы (2020)
Genome-wide association studies have identified breast cancer risk variants in over 150 genomic
РОЛЬ ДЛИННЫХ НЕКОДИРУЮЩИХ РНК В БИОЛОГИИ ОПУХОЛЕЙ
THE ROLE OF LONG, NON-CODING RNA IN THE BIOLOGY OF TUMORS
Beylerli O. A., Gareev I. F., БЕЙЛЕРЛИ, О. А., ГАРЕЕВ, И. Ф. (2020)
GENOME
Анализ ассоциаций с рассеянным склерозом генетических маркеров предрасположенности, выявленных в результате полногеномных исследований
The analysis of association between multiple sclerosis and genetic markers identified in genome-wide association studies
ТИМАШЕВА, Я.Р., НАСИБУЛЛИН, Т.Р., ТУКТАРОВА, И.А., ЭРДМАН, В.В., ГАЛИУЛЛИН, Т.Р., ЗАПЛАХОВА, О.В., БАХТИЯРОВА, К.З., МУСТАФИНА, О.Е., TIMASHEVA, Y.R., NASIBULLIN, T.R., TUKTAROVA, I.A., ERDMAN, V.V., GALIULLIN, T.R., ZAPLAKHOVA, O.V., BAKHTIIAROVA, K.Z., MUSTAFINA, O.E. (2020)
The analysis of association between multiple sclerosis and genetic markers identified in genome
МЕХАНИЗМЫ ВОЗНИКНОВЕНИЯ И ЭВОЛЮЦИИ БЕЛОК-КОДИРУЮЩИХ ГЕНОВ
BASIC MECHANISMS OF THE ORIGIN AND EVOLUTION OF PROTEIN-CODING GENES
МУСТАФИН, Р.Н., MUSTAFIN, R.N. (2020)
Non-coding RNAs as therapeutic targets in spinal cord injury
Beylerli, O.A., Azizova, S.T., Konovalov, N.A., Akhmedov, A.D., Gareev, I.F., Belogurov, A.A. (2020)
. The results of international sequencing of the human genome were analyzed in 2004. These data revealed about
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)
GENOMICS
Interrelation of Telomeres with Transposable Elements in Aging
Mustafin, R. N. (2020)
processes in the genome conditioned by the regulatory influence of transposable elements
GENOME-WIDE ASSOCIATION STUDY IDENTIFIES 32 NOVEL BREAST CANCER SUSCEPTIBILITY LOCI FROM OVERALL AND SUBTYPE-SPECIFIC ANALYSES
ZHANG, H., AHEARN, T.U., CHANOCK, S.J., HOOVER, R.N., KOUTROS, S., YANG, X.R., GARCÍA-CLOSAS, M., QI, G., ZHAO, N., CHATTERJEE, N., LECARPENTIER, J., BARNES, D., DUNNING, A.M., PHAROAH, P.D.P, EASTON, D.F., BEESLEY, J., O’MARA, T.A., PARSONS, M.T., CHENEVIX-TRENCH, G., JIANG, X., TAMIMI, R.M., KRAFT, P., BOLLA, M.K., DENNIS, J., WANG, Q., ESLIE, G., BERMISHEVA, M., KHUSNUTDINOVA, E. (2020)
subtype1–3. To identify novel loci, we performed a genome-wide association study including 133,384 breast
LYNCH SYNDROME GERMLINE MUTATIONS IN BREAST CANCER: NEXT GENERATION SEQUENCING CASE-CONTROL STUDY OF 1,263 PARTICIPANTS
NIKITIN, A.G., CHUDAKOVA, D.A., ENIKEEV, R.F., GORDIEV, M.G., SAKAEVA, D., DRUZHKOV, M., SHIGAPOVA, L.H., BROVKINA, O.I., SHAGIMARDANOVA, E.I., GUSEV, O.A. (2020)
Genome instability—the increased tendency of acquiring mutations in the genome and ability of a

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