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NEURAL NETWORK MODEL AS THE MULTIDISCIPLINARY TEAM MEMBER IN CLINICAL DECISION SUPPORT TO AVOID MEDICAL MISTAKES (ALYNX CONCEPT)
Buzaev, Igor V., Plechev, Vladimir V., Nikolaeva, Irina E., Galimova, Rezida (2017)
NEURAL NETWORK MODEL AS THE MULTIDISCIPLINARY TEAM MEMBER IN CLINICAL DECISION SUPPORT TO AVOID
MOLECULAR DOCKING AND PRECLINICAL STUDY OF FIVE-MEMBERED S,S-PALLADAHETEROCYCLE AS HEPATOPROTECTIVE AGENT
AKHMADIEV, N.S., AKHMETOVA, V.R., IBRAGIMOV, A.G., GALIMOVA, A.M., GALIMOVA, R.A., AGLETDINOV, E.F., KATAEV, V.A., KHAIRULLINA, V.R. (2019)
providing a basis for the therapeutic effects of five-membered palladacycles (as mixture of stereoisomers
Genetic predictors of sick sinus syndrome
Timasheva, Y, Badykov, M, Akhmadishina, L, Nasibullin, T, Badykova, E, Pushkareva, A, Plechev, V, Sagitov, I, Zagidullin, N (2021)
KCNE1 (potassium voltage-gated channel subfamily E member 1)
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Coignard, J., Lush, M., Beesley, J., O’Mara, T.A., Dennis, J, Tyrer, J.P., Barnes, D.R., McGuffog, L., Leslie, G., Bolla, M.K., Adank, M.A., Kiiski, J.I., Nevanlinna, H., team of authors (2021)
КЛИНИЧЕСКИЙ И МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ АНАЛИЗ СЛУЧАЯ СЕМЕЙНОГО РАССЕЯННОГО СКЛЕРОЗА В РЕСПУБЛИКЕ БАШКОРТОСТАН
CLINICAL AND MOLECULAR GENETIC ANALYSIS OF A CASE OF FAMILIAL MULTIPLE SCLEROSIS IN THE REPUBLIC OF BASHKORTOSTAN
Заплахова, О.В., Тимашева, Я.Р., Бахтиярова, К.З., Туктарова, И.А., Мустафина, О.Е., Zaplakhova, O.V., Timasheva, Y.R., Bakhtiyarova, K.Z., Tuktarova, I.A., Mustafina, O.E. (2019)
of six affected members of one family. Material and methods. Six members of the family of Russian ethnic
MICRORNA-200 FAMILY EXPRESSION ANALYSIS IN METASTATIC CLEAR CELL RENAL CELL CARCINOMA PATIENTS
GILYAZOVA, I.R., KLIMENTOVA, E.A., BERMISHEVA, M.A., KHUSNUTDINOVA, E.K., IZMAILOV, A.A., GALIMOVA, E.F., SAFIULLIN, R.I., GALIMOV, S.N., V.N. Pavlov, BULYGIN, K.V. (2020)
The aim of this study is to analyse the of expression levels of microRNA-200 family members
Клинический и молекулярно-генетический анализ случая семейного рассеянного склероза
CLINICAL AND MOLECULAR GENETIC ANALYSIS OF A CASE OF FAMILIAL MULTIPLE SCLEROSIS IN THE REPUBLIC OF BASHKORTOSTAN
ЗАПЛАХОВА, О.В., ТИМАШЕВА, Я.Р., БАХТИЯРОВА, К.З., ТУКТАРОВА, И.А., МУСТАФИНА, О.Е., TIMASHEVA Y.R., ZAPLAKHOVA O.V., BAKHTIYAROVA K.Z., TUKTAROVA I.A., MUSTAFINA O.E. (2019)
iASPP protects the heart from ischemia injury by inhibiting p53 expression and cardiomyocyte apoptosis
Yagudin, T, Zhao, Y, Gao, HY, Zhang, Y, Yang, Y, Zhang, XF, Ma, WB, Daba, TM, Ishmetov, V, Kang, K, Yang, BF, Pan, ZW (2021)
-stimulating protein of p53 (iASPP) is a member of the ASPP family proteins and an evolutionarily preserved inhibitor
Case Report: Coil Occlusion of Two Congenital Coronary Cameral Fistulas Connecting Right and Left Circumflex Arteries to the Right Ventricle: An Innovative Stent-Assisted Technique
Buzaev, IV, Plechev, VV, Khalikova, G, Khabirova, K, Nikolaeva, IE, Onorato, EM (2022)
. After heart team discussion, with the aim to reduce the risk of embolization, an innovative stent
A NOVEL PATHOGENIC VARIANT C.975G>A (P.TRP325*) IN THE POU3F4 GENE IN YAKUT FAMILY (EASTERN SIBERIA, RUSSIA) WITH THE X-LINKED DEAFNESS-2 (DFNX2)
BARASHKOV, N.A., KLAROV, L.A., TERYUTIN, F.M., SOLOVYEV, A.V., PSHENNIKOVA, V.G., ROMANOV, G.P., TOMSKY, M.I., FEDOROVA, S.A., KONNIKOVA, E.E., TOBOKHOV, A.V., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L., DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2018)
members of this family revealed both already known (mixed progressive hearing loss) and additional

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