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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)
many causes including defects in DNA repair systems. Previously, it has been shown that germline
THE FANCM:P.ARG658* TRUNCATING VARIANT IS ASSOCIATED WITH RISK OF TRIPLE-NEGATIVE BREAST CANCER
Bogliolo, M., Catucci, I., Caleca, L., Lasheras, S.V., Pujol, R., Kiiski, J.I., Muranen, T.A., Barnes, D.R., Dennis, J., Michailidou, K., Bolla, M.K., Leslie, G., Figlioli, G. (2019)
variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk
ASSOCIATION OF 22 POTENTIAL PATHOGENIC VARIANTS OF NEW CANDIDATE GENES AND THE RISK OF OVARIAN CANCER
Mingazheva, E.T., Prokofyeva, D.S., Valova, Ya.V., Andreeva, E.A., Nurgalieva, A.Kh., Valiev, R.R., Ekomasova, N.V., Faishanova, R.R., Romanova, A.R., Khusnutdinova, E.K. (2022)
involved in the disease. As a result of previous exome sequencing of DNA samples from breast cancer Germany
SYNTHESIS AND NOOTROPIC ACTIVITY OF NEW 3-AMINO-12-N-METHYLCYTISINE DERIVATIVES
Tsypysheva, I.P., Kovalskaya, A.V., Lobov, A.N., Makara, N.S., Petrova, P.R., Farafontova, E.I., Zainullina, L.F., Vakhitova, Yu.V., Zarudii, F.S. (2015)
DNA-binding activity). The cytotoxicity of the synthesized compounds was assessed. The lead compound
CLINICAL FORMS OF HUNTINGTON’S DISEASE IN THE PATIENTS FROM REPUBLIC OF BASHKORTOSTAN
Magzhanov, R., Saifullina, E. (2014)
features of HD and DNA-diagnostics will help to early diagnosis and effective genetic counselling
Interrelation of Telomeres with Transposable Elements in Aging
Mustafin, R. N. (2020)
. This is due to the ability of ribozymes and peptides to interact with specific sequences of DNA nucleotides
Genome-Wide Association Study: Analysis of Association of Polymorphic Loci in 4p15.2 and 20q13.31 Regions with Paranoid Schizophrenia
Gareeva, A.E. (2023)
healthy individuals. GWAS genotyping of DNA samples was carried out on the PsychChip, which included 610
Novel Genetic Risk Marker for Paranoid Schizophrenia in the Chromosomal Region 9q21.13 in Tatars: A Genome-Wide Association Analysis
Gareeva, A.E. (2024)
of Bashkortostan. Genome-wide genotyping of DNA samples was carried out on the PsychChip biochip, which included
Searching for Ethnospecific Risk Markers of Paranoid Schizophrenia in Bashkirs Based on the Results from Genome-Wide Association Study
Gareeva, A.E. (2024)
individuals. Genome-wide genotyping of DNA samples was carried using a PsychChip biochip, which included
Genome-Wide Analysis of the Risk Association for the Development of Paranoid Schizophrenia in Russians: Search for Genetic Markers in the 1q43 Chromosomal Region
Gareeva, A.E. (2024)
genotyping of DNA samples was carried out on the PsychChip biochip, which included 610 000 single nucleotide

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