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Prostate Cancer: Genetics, Epigenetics and the Need for Immunological Biomarkers
Rafikova, Guzel, Gilyazova, Irina, Enikeeva, Kadriia, Pavlov, Valentin, Kzhyshkowska, Julia (2023)
with various factors, including age, heredity, and race. Recent research in prostate cancer genetics has
CXCL13 POLYMORPHISM IS ASSOCIATED WITH ESSENTIAL HYPERTENSION IN TATARS FROM RUSSIA
TIMASHEVA, YA.R., NASIBULLIN, T.R., TUKTAROVA, I.A., ERDMAN, V.V., MUSTAFINA, O.E (2018)
=0.008) and dominant (OR 0.41, PFDR 4.38×10−4 ) genetic model. The analysis of gene–gene interactions
OPINIONS OF HEARING PARENTS ABOUT THE CAUSES OF HEARING IMPAIRMENT OF THEIR CHILDREN WITH BIALLELIC GJB2 MUTATIONS
Solovyev, A.V., Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Bady-Khoo, M.S., Lobov, S.L., Popova, N.Y., Romanov, G.P., Sazonov, N.N., Bondar, A.A., Morozov, I.V., Tomsky, M.I., Fedorova, S.A., Khusnutdinova, E.K. (2017)
sensory disorder. The results of the molecular-based studies of HI are widely used in various genetic test
Population Characteristics of the Spectrum and Frequencies of CFTR Gene Mutations in Patients with Cystic Fibrosis from the Republic of Bashkortostan (Russia)
Ayupova, Guzel, Litvinov, Sergey, Akhmetova, Vita, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)
. In particular it is possible to choose certain test kits for quick and effective genetic screening before use
Genetic Predictors of Antipsychotic Efflux Impairment via Blood-Brain Barrier: Role of Transport Proteins
Nasyrova, Regina F., Shnayder, Natalia A., Osipova, Sofia M., Khasanova, Aiperi K., Efremov, Ilya S., Al-Zamil, Mustafa, Petrova, Marina M., Narodova, Ekaterina A., Garganeeva, Natalia P., Shipulin, German A. (2023)
of AP-induced ADRs is a genetically-determined impairment of AP efflux across the blood-brain barrier
Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes
Timasheva, Y., Balkhiyarova, Z., Avzaletdinova, D., Rassoleeva, I., Morugova, T.V., Korytina, G., Prokopenko, I., Kochetova, O. (2023)
We tested associations between 13 established genetic variants and type 2 diabetes (T2D) in 1371
GENETIC DETERMINANTS OF ESSENTIAL HYPERTENSION IN THE POPULATION OF TATARS FROM RUSSIA
Timasheva, Y., Nasibullin, T., Imaeva, E., Mirsaeva, G., Mustafina, O. (2016)
is characterized by a unique combination of European and Asian genetic ancestry, and is an interesting object
МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ АНАЛИЗ СЛУЧАЯ ЧАСТИЧНОЙ ДЕЛЕЦИИ Y-ХРОМОСОМЫ В СУДЕБНО-МЕДИЦИНСКОЙ ПРАКТИКЕ
MOLECULAR-GENETIC ANALYSIS OF A RARE FORENSIC CASE OF PARTIAL DELETION OF THE Y-CHROMOSOME
ТИМАШЕВА, Я.Р., ТУКТАРОВА, И.А., ГИЗУЛЛИНА, Л.И., СУНДЫРЕВ, Е.Ю., МУСТАФИНА, О.Е., Timasheva Ya.R., Tuktarova I.A., Gizullina L.I., Sundyrev E.Yu., Mustafina O.E. (2019)
MOLECULAR-GENETIC ANALYSIS OF A RARE FORENSIC CASE OF PARTIAL DELETION OF THE Y-CHROMOSOME
Breast cancer risk genes - Association analysis in more than 113,000 women
Dorling, L., Carvalho, S., Allen, J., González-Neira, A., Luccarini, C., Wahlström, C., Pooley, K.A., Parsons, M.T., Fortuno, C., Wang, Q., Bolla, M.K., Dennis, J., Bermisheva, M., Khusnutdinova, E., Prokofyeva, D., other additional authors (2021)
BACKGROUND Genetic testing for breast cancer susceptibility is widely used, but for many genes
Mendelian Randomization Analysis Identifies Inverse Causal Relationship between External Eating and Metabolic Phenotypes
Timasheva, Yanina, Balkhiyarova, Zhanna, Avzaletdinova, Diana, Morugova, Tatyana, Korytina, Gulnaz F., Nouwen, Arie, Prokopenko, Inga, Kochetova, Olga (2024)
phenotypes remain unclear. We aimed to identify genetic variants linked to eating behaviour and investigate

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