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Bioinformatics Analysis Screening and Identification of Key Biomarkers and Drug Targets in Human Glioblastoma
Wang, Chunlei, Beylerli, Ozal, Gu, Yan, Xu, Shancai, Ji, Zhiyong, Ilyasova, Tatiana, Gareev, Ilgiz, Chekhonin, Vladimir (2024)
led to a significant advancement in gene expression analysis platforms. Microarray analysis has gained
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)
Russia. The main- and gene-based effects of 12 SNPs in SLC6A4 (5-HTTLPR, rs1042173), HTR2A (rs7322347
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)
detected in two patients. Genes located in the area of imbalance were KLF1, DNASE2, and GCDH. Patients
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
ВЛИЯНИЕ НОКАУТА ПО ГЕНАМ TLR9 И AIM2 В ОПУХОЛЕВЫХ КЛЕТКАХ MCF7 НА ИЗМЕНЕНИЕ ТРАНСКРИПЦИОННОЙ АКТИВНОСТИ МАРКЕРНЫХ ГЕНОВ ОКСИДАТИВНОГО СТРЕССА И ГИПОКСИИ ПОД ВОЗДЕЙСТВИЕМ ГЦ-ОБОГАЩЕННЫХ ФРАГМЕНТОВ ДНК
EFFECT OF TLR9/AIM2 GENE KNOCKOUT IN MCF7 TUMOR CELLS ON ALTERATIONS OF OXIDATIVE STRESS AND HYPOXIA MARKER GENE EXPRESSION IN RESPONSE TO GC-ENRICHED DNA FRAGMENTS
Малиновская, Е.М., Кожина, Е.А., Ершова, Е.С., Конькова, М.С., Вейко, В.П., Бобровский, П.А., Лазарев, В.Н., Каменева, Л.В., Писарев, В.М., Вейко, Н.Н., Костюк, С.В., Malinovskaya, E.M., Kozhina, E.A., Ershova, E.S., Kon’kova, M.S., Veiko, V.P., Bobrovsky, P.A., Lazarev, V.N., Kameneva, L.V., Pisarev, V.M., Veiko, N.N., Kostyuk, S.V. (2020)
TLR9 и AIM2, коди рующих внутриклеточные сенсорные молекулы ДНК. Материал и методы. Исследование
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)
REPLICATIVE STUDY OF GWAS-ASSOCIATED CANDIDATE GENE LOCI IN PATIENTS WITH OSTEOARTHRITIS FROM
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)
QTL) reported in these tissues, we identify 26 previously unreported, likely target genes of overall breast
ATYPICAL CLINICAL MANIFESTATIONS AND GENOTYPE-PHENOTYPE CORRELATIONS OF NEUROFIBROMATOSIS TYPE 1
Мустафин, Р.Н., Mustafin, R.N. (2022)
by specific mutations in the NF1 gene (causing substitutions of amino acids in neurofibromin: p.Arg1038, p
Role of Neurotransmitter System Genes in Chronic Obstructive Pulmonary Disease
Korytina, GF, Akhmadishina, LZ, Kochetova, OV, Nasibullin, TR, Aznabaeva, YG, Zulkarneev, SR, Izmailova, SM, Zagidullin, SZ, Victorova, TV (2021)
of the respiratory system. Smoking is a major risk factor of COPD. Neurotransmitter system genes were tested
ROLE OF NEUROTRANSMITTER SYSTEM GENES IN CHRONIC OBSTRUCTIVE PULMONARY DISEASE
KORYTINA, G.F., AKHMADISHINA, L.Z., KOCHETOVA, O.V., NASIBULLIN, T.R., AZNABAEVA, Y.G., ZULKARNEEV, S.R., IZMAǏLOVA, S.M., ZAGIDULLIN, S.Z., VICTOROVA, T.V. (2021)
of the respiratory system. Smoking is a major risk factor of COPD. Neurotransmitter system genes were tested

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