По вашему запросу найдено документов: 80

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Prospects for the treatment of neurofibromatosis type 1: A review
Mustafin, R.N., Мустафин, Р.Н. (2022)
mutations in NF1 gene. Protein product of NF1 is a neurofibromin, which inhibits RAS-RAF-MEK-ERK system
Osteogenesis Imperfecta: Search for Mutations in Patients from the Republic of Bashkortostan (Russia)
Nadyrshina, D., Zaripova, A., Tyurin, A., Minniakhmetov, I., Zakharova, E., Khusainova, R. (2022)
, and 1 mutation in P3H1 and IFIMT5 genes were found in isolated states; 11 of them were not previously
Relationship between glucose homeostasis and obesity in early life-a study of Italian children and adolescents
Balkhiyarova, Z., Luciano, R., Kaakinen, M., Ulrich, A., Shmeliov, A., Bianchi, M., Chioma, L., Dallapiccola, B., Prokopenko, I., Manco, M. (2022)
there was no effect of FG/FI levels on BMI. Our results demonstrate that the glycaemic and T2D risk genetic variants
Гепатоцеллюлярная карцинома: этиологические факторы и механизмы развития. Обзор литературы
Hepatocellular Carcinoma: Aetiology and Mechanisms of Development. A Literature Review
К. В. Меньшиков, K. V. Menshikov, А. В. Султанбаев, A. V. Sultanbaev, Ш. И. Мусин, Sh. I. Musin, И. Р. Рахматуллина, I. R. Rakhmatullina, И. А. Меньшикова, I. A. Menshikova, Р. Р. Абдеев, R. R. Abdeev, Н. И. Султанбаева, N. I. Sultanbaeva, Е. В. Попова, E. V. Popova, Г. А. Серебренников, G. A. Serebrennikov (Креативная хирургия и онкология, №2, 2022)
The role of retroelements in the development of hereditary tumor syndromes
Mustafin, R.N., Khusnutdinova, E.K., Мустафин, Р.Н., Хуснутдинова, Э.К. (2022)
Genetic Predisposition to Schizophrenia and Depressive Disorder Comorbidity
Shnayder, N.A., Novitsky, M.A., Neznanov, N.G., Limankin, O.V., Asadullin, A.R., Petrov, A.V., Dmitrenko, D.V., Narodova, E.A., Popenko, N.V., Nasyrova, R.F. (2022)
and depression are polygenic. The most studied candidate genes are GRIN1, GPM6A, SEPTIN4, TPH1, TPH2, CACNA1C
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)
target genes
Dissecting and analyzing the Subclonal Mutations Associated with Poor Prognosis in Diffuse Glioma
Bai, Ming, Wang, Xiaolong, Zhang, Huixue, Wang, Jianjian, Lyaysan, Gaysina, Xu, Si, Tian, Kuo, Wang, Tianfeng, Li, Jie, Wang, Na, Lu, Xiaoyu, Zhang, Xiaoming, Wang, Lihua (2022)
and subclonal mutations for most mutant genes. Based on the clonal status of a given gene, we systematically
ПОЗНАВАТЕЛЬНАЯ РОЛЬ МЕТОДА МОДЕЛИРОВАНИЯ В УСВОЕНИИ КУРСА ПАТОФИЗИОЛОГИИ
THE COGNITIVE ROLE OF THE MODELING METHOD IN MASTERING THE COURSE OF PATHOPHYSIOLOGY
Еникеев, Д.А., Хисамов, Э.Н., Еникеев, О.А., Срубилин, Д.В., Габдрахманова, И.Д., Enikeev, D.A., Hisamov, E.N., Enikeev, O.A., Srubilin, D.V., Gabdrakhmanova, I.D. (2022)
Circulating miRNAs as Diagnostic and Prognostic Biomarkers in High-Grade Gliomas
Wu, JN, Al-Zahrani, A, Beylerli, O, Sufianov, R, Talybov, R, Meshcheryakova, S, Sufianova, G, Gareev, I, Sufianov, A (2022)
RNAs and their gene-targets (PDCD4, WNT5A, MET, and EGFR) in high-grade gliomas. Quantitative reverse transcription

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