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Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga–Ural Region
Khidiyatova, Irina, Khidiyatova, Indira, Zinchenko, Rena, Marakhonov, Andrey, Karunas, Alexandra, Avkhadeeva, Svetlana, Aznzbaev, Marat, Khusnutdinova, Elza (2023)
Hereditary cataracts are characterized by significant clinical and genetic heterogeneity, which can
Genetic Biomarkers of Antipsychotic-Induced Prolongation of the QT Interval in Patients with Schizophrenia
Vaiman, E.E., Shnayder, N.A., Zhuravlev, N.M., Petrova, M.M., Asadullin, A.R., Al-Zamil, M., Garganeeva, N.R., Shipulin, G.A., Cumming, G., Nasyrova, R.F. (2022)
, and monotherapy, etc.) and non-modifying factors (genetic predisposition, gender, age, etc.). The genetic
The use of bioinformatic analysis to study intracerebral hemorrhage
Gareev, Ilgiz, Beylerli, Ozal, Ilyasova, Tatiana, Mashkin, Andrey, Shi, Huaizhang (2024)
in elucidating the genetic, molecular, and environmental underpinnings of ICH. Through a detailed examination
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
ДИАГНОСТИКА И ЛЕЧЕНИЕ РАКА ЯИЧНИКОВ В СВЕТЕ СОВРЕМЕННЫХ МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИХ ДОСТИЖЕНИЙ
DIAGNOSIS AND TREATMENT OF OVARIAN CANCER IN THE LIGHT OF MODERN MOLECULAR GENETIC ACHIEVEMENTS
Kagirova, E.M., Khusainova, R.I., Minniakhmetov, I.R., Кагирова, Э.М., Хусаинова, Р.И., Минниахметов, И.Р. (2023)
DIAGNOSIS AND TREATMENT OF OVARIAN CANCER IN THE LIGHT OF MODERN MOLECULAR GENETIC ACHIEVEMENTS
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
Наследственные заболевания человека со скелетной патологией – молекулярный патогенез и клиническая характеристика
Hereditary human diseases with skeletal pathology – molecular pathogenesis and clinical characteristics
Valeeva, Diana I., Khusainova, Rita I., Khusainova, Leonora N., Tyurin, Anton V., Валеева, Д.И., Хусаинова, Р.И., Хусаинова, Л.Н., Тюрин, А.В. (2024)
Hereditary human diseases with skeletal pathology – molecular pathogenesis and clinical
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
ИЗУЧЕНИЕ РОЛИ МОЛЕКУЛЯРНО-БИОЛОГИЧЕСКИХ МАРКЕРОВ ДЛЯ КЛИНИЧЕСКОГО ПРИМЕНЕНИЯ В ОНКОЛОГИИ
STUDY OF THE ROLE OF MOLECULAR BIOLOGICAL MARKER FOR CLINICAL APPLICATION IN ONCOLOGY
Ч. Х. Валиахметова, Ch. Кh. Valiakhmetova, А. А. Гарайшина, A. A. Garaishina, Д. Д. Сакаева, D. D. Sakaeva (Креативная хирургия и онкология, №3, 2017)
STUDY OF THE ROLE OF MOLECULAR BIOLOGICAL MARKER FOR CLINICAL APPLICATION IN ONCOLOGY
ПРОБЛЕМЫ И ДОСТИЖЕНИЯ В ИЗУЧЕНИИ КЛИНИКО-ГЕНЕТИЧЕСКИХ АСПЕКТОВ МУКОВИСЦИДОЗА
PROBLEMS AND ACHIEVEMENTS IN THE STUDY OF CLINICAL AND GENETIC ASPECTS OF CYSTIC FIBROSIS
АЮПОВА, Г.Р., МИННИАХМЕТОВ, И.Р., ХУСАИНОВА, Р.И., AYUPOVA, G.R., MINNIAKHMETOV, I.R., KHUSAINOVA, R.I. (2022)
PROBLEMS AND ACHIEVEMENTS IN THE STUDY OF CLINICAL AND GENETIC ASPECTS OF CYSTIC FIBROSIS

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