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Bioinformatics analysis of potential therapeutic targets for COVID-19 infection in patients with carotid atherosclerosis
Yanchao, L., Sibin, Z., Gareev, I., Huan, X., Junfei, Z., Chunyang, L., Beylerli, O., Sufianov, A., Chao, Y., Yuyan, G., Xun, X., Ahmad, A. (2022)
Differentially expressed genes
LONG NON-CODING RNA ASB16-AS1 ENHANCES CELL PROLIFERATION, MIGRATION AND INVASION VIA FUNCTIONING AS A CERNA THROUGH MIR-1305/WNT/β-CATENIN AXIS IN CERVICAL CANCER
LIU, W., ZHUANG, R., BAI, X., JIA, Z., KAPORA, E., TAN, W., FENG, S. (2020)
the effect of ASB16-AS1 on CC via regulating miR-1305. Methods: Differentially expressed lncRNAs associated
DOWNREGULATION OF LONG NON-CODING RNA KCNQ1OT1: AN IMPORTANT MECHANISM OF ARSENIC TRIOXIDE-INDUCED LONG QT SYNDROME
Jiang, Y., Du, W., Chu, Q., Qin, Y., Tuguzbaeva, G., Wang, H., Li, A., Li, G., Li, Y., Chai, L., Yue, E., Sun, X., Wang, Z., V.N. Pavlov, Yang, B., Bai, Y. (2018)
synthesized to knockdown lncRNA Kcnq1ot1. Results: After ATO treatment, the Kcnq1ot1 and Kcnq1 expression
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)
, specifically adipose tissue and immune cells from blood and spleen. Using expression quantitative trait loci (e
Construction of lncRNA-associated ceRNA networks to identify prognostic lncRNA biomarkers for glioblastoma
LIU, Z., WANG, X., YANG, G., ZHONG, C., ZHANG, R., YE, J., ZHONG, Y., HU, J., OZAL, B., ZHAO, S. (2020)
of their mechanism of action in GBM. We downloaded data from The Cancer Genome Atlas (TCGA) and the Gene Expression
PROSPECTS IN THE SEARCH FOR PEPTIDES FOR SPECIFIC REGULATION OF AGING
MUSTAFIN, R.N., KHUSNUTDINOVA, E.K. (2019)
and the key role of transposons in the regulation of gene expression during ontogenesis. The silencing
Exosomal miR-2276-5p in Plasma Is a Potential Diagnostic and Prognostic Biomarker in Glioma
Sun, J.X., Sun, Z.Y., Gareev, I, Yan, T, Chen, X, Ahmad, A, Zhang, D.M., Zhao, B.X., Beylerli, O., Yang, G., Zhao, S.G. (2021)
to quantitative real-time polymerase chain reaction (qRT-PCR) analysis for the exosomal miR-2276-5p expression
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)
expression and functioning of encoded proteins. To explain these associations, we suggested the role
CIRCULATING MICRORNAS AS POTENTIAL NONINVASIVE BIOMARKERS OF SPONTANEOUS INTRACEREBRAL HEMORRHAGE
GAREEV, I., YANG, G., SUN, J., BEYLERLI, O., CHEN, X., ZHANG, D., ZHAO, B., ZHANG, R., SUN, Z., YANG, Q., LI, L., ZHAO, S., PAVLOV, V., SAFIN, S. (2020)
reaction analyses for the expression levels of circulating miR-181b, miR-223, miR-155, and miR-145. Results
Circulating miRNAs as Diagnostic and Prognostic Biomarkers in High-Grade Gliomas
Wu, JN, Al-Zahrani, A, Beylerli, O, Sufianov, R, Talybov, R, Meshcheryakova, S, Sufianova, G, Gareev, I, Sufianov, A (2022)
on microRNAs (miRNAs) expression profiling in glioma and highlighted the most frequently dysregulated mi

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