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ANALYSIS OF PRIMARY DIAGNOSTICS OF HEREDITARY MOTOR AND SENSORY NEUROPATHIES IN THE REPUBLIC OF BASHKORTOSTAN
Сайфуллина, Е.В., Магжанов, Р.В., Хидиятова, И.М., Хуснутдинова, Э.К., Saifullina, E.V., Magzhanov, R.V., Khidiiatova, I.M., Khusnutdinova, E.K. (2017)
molecular and genetic diagnostics.Objective. Analysis of primary diagnostics of HMSN for subsequent
The Role of Polymorphic Variants of Gene Components of the PTEN/PI3K/AKT Signaling Pathway in the Development of Prostate Cancer
Gilyazova, I.R., Ivanova, E.A., Bermisheva, M.A., Loginova, M.V., Asadullina, D.D., Ishemgulov, R.R., Mustafin, A.T., Pavlov, V.N., Khusnutdinova, E.K. (2022)
be used to create a panel of molecular markers for disease prognosis and assessment of tumor
GENETIC ASPECTS OF KERATOCONUS DEVELOPMENT
Bikbova, M.M., Usubova, E.L., Oganisyana, K.Kh., Lobov, S.L., Khasanovad, R.R., Dzhemilevab, L.U., Khusnutdinova, E.K. (2017)
topography and its thinning, stretching, and protrusion. The hereditary or genetic theory of keratoconus
ГЕНЕТИЧЕСКИЕ МАРКЕРЫ ОСТЕОАРТРИТА У ЖЕНЩИН С НЕДИФФЕРЕНЦИРОВАННОЙ ДИСПЛАЗИЕЙ СОЕДИНИТЕЛЬНОЙ ТКАНИ
SEARCH FOR OSTEOARTHRITIS GENETIC MARKERS IN WOMEN WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA
Khusainova, R.I., Tyurin, A.V., Shapovalova, D.A., Khusnutdinova, E.K., Хусаинова Р.И., Тюрин А.В., Шаповалова Д.А., Хуснутдинова Э.К. (2017)
). On the basis of clinical and genetic data, we revealed statistically significant models to predict
INVESTIGATION OF THE ROLE OF MICRORNA ASSOCIATED WITH THE VHL-HIFα-DEPENDENT PATHWAY IN PATIENTS WITH CLEAR CELL RENAL CELL CARCINOMA
KLIMENTOVA, E.A., GILYAZOVA, I.R., BERMISHEVA, M.A., BLINNIKOVA, A. M., SAFIULLIN, R.I., IZMAILOV, A.A., YANG, B., PAVLOV ., V.N, KHUSNUTDINOVA, E.K. (2020)
, which will make it possible both to identify new molecular markers of the risk of developing the disease
ЭПИГЕНЕТИКА СУИЦИДАЛЬНОГО ПОВЕДЕНИЯ
EPIGENETICS OF SUICIDAL BEHAVIOR
МУСТАФИН, Р.Н., КАЗАНЦЕВА, А.В., ЕНИКЕЕВА, Р.Ф., ДАВЫДОВА, Ю.Д., МАЛЫХ, С.Б., ВИКТОРОВ, ВИТАЛИЙ ВАСИЛЬЕВИЧ, ХУСНУТДИНОВА, Э.К., Mustafin R.N., , Kazantseva A.V., Enikeeva R.F., Davydova Yu.D., Malykh S.B., Viktorov V.V., Khusnutdinova E.K. (2019)
Генетические механизмы когнитивного развития
GENETIC MECHANISMS OF COGNITIVE DEVELOPMENT
Мустафин, Р. Н., Казанцева, А.В., Малых, С.Б, Хуснутдинова, Е.К., MUSTAFIN R.N., KAZANTSEVA A. V., MALYKH S. B., KHUSNUTDINOVA E.K. (2020)
GENETIC MECHANISMS OF COGNITIVE DEVELOPMENT
Исследование профилей экспрессии экзосомальных микроРНК-126 и микроРНК-218 у пациентов с геморрагической лихорадкой с почечным синдромом (ГЛПС)
Study of the exosomal microRNA-126 and microRNA-218 expression profiles in patients with hemorrhagic fever with renal syndrome (HFRS)
Гилязова, И.Р., Хасанова, Г.М., Иванова, Е.А., Асадуллина, Д.Д., Хасанова, А.Н., Измайлов, А.А., Гилязова, Г.Р., Ван, Гоцин, Хуан, Хунлин, Пан, Цзяхуэй, Шао, Тун, Яо, Хаочен, Ван, Вэньфан, Хуснутдинова, Э.К., Gilyazova, I.R., Khasanova, G.M., Ivanova, E.A., Asadullina, D.D., Khasanova, A.N., Izmailov, A.A., Gilyazova, G.R., Wang, Guoqing, Huang, Honglan, Pan, Jiahui, Shao, Tong, Yao, Haochen, Wang, Wenfang, Khusnutdinova, E.K. (2022)
A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)
of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes
GENETIC ASSOCIATION OF ADRA2A AND ADRB3 GENES WITH METABOLIC SYNDROME AMONG THE TATARS
Kochetova, O.V., Viktorova, T.V., Mustafina, O.E., Karpov, A.A., Khusnutdinova, E.K. (2015)
An association study was performed for genetic polymorphisms in ADRB3 (rs4994) and ADRA2A (rs

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