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По вашему запросу найдено документов: 81

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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)

of the pathophysiology and/or genetic predictors of these mental disorders. The aim of this study was to review

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

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

ПОЛИГЕННЫЙ АНАЛИЗ НАСЛЕДСТВЕННОЙ ПРЕДРАСПОЛОЖЕННОСТИ К ЭССЕНЦИАЛЬНОЙ ГИПЕРТЕНЗИИ

POLYGENIC ANALYSIS OF GENETIC SUSCEPTIBILITY TO ESSENTIAL HYPERTENSION

ТИМАШЕВА, Я.Р., ГЕРАСИМОВА, К.А., ТУКТАРОВА, И.А., ЭРДМАН, В.В., НАСИБУЛЛИН, Т.Р., TIMASHEVA, Y.R., GERASIMOVA, K.A., TUKTAROVA, I.A., ERDMAN, V.V., NASIBULLIN, T.R. (2022)

POLYGENIC ANALYSIS OF GENETIC SUSCEPTIBILITY TO ESSENTIAL HYPERTENSION

Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review

Tyurin, Anton, Merkuryeva, Elena, Zaripova, Aliya, Markova, Tatyana, Nagornova, Tatyana, Dantsev, Ilya, Nadyrshina, Dina, Zakharova, Ekaterina, Khusainova, Rita (2022)

, a clinical and genetic analysis of 12 cases with molecularly confirmed OI type V from 12 unrelated

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)

part of the genetic background. We aimed to test if weighted genetic risk scores (GRSs) for T2D

Герминальные мутации как возможные биомаркеры эффективности терапии ингибиторами контрольных точек иммунитета у пациентов с почечно-клеточной карциномой (мини-обзор)

Germline mutations as possible biomarkers of immune checkpoint inhibitor therapy efficacy in patients with renal cell carcinoma (mini review)

genetics

SIGNALING PATHWAYS AND THERAPEUTIC APPROACHES IN GLIOBLASTOMA MULTIFORME (REVIEW)

KHABIBOV, M., GARIFULLIN, A., KHAMITOV, F., KHALIKOVA, L., BOUMBER, Y., KHADDOUR, K., FERNANDEZ, M., KUZNETSOVA, N., KIT, O., KHARIN, L. (2022)

and is associated with a poor clinical prognosis. Despite the progress in the understanding of the molecular

Aging of mesenchymal stem cell: machinery, markers, and strategies of fighting

Al-Azab, Mahmoud, Safi, Mohammed, Idiiatullina, Elina, Al-Shaebi, Fadhl, Zaky, Mohamed Y. (2022)

major challenge in front of cellular therapy advancement. Many factors, ranging from genetic

ФАКТОРНЫЙ АНАЛИЗ РИСКА РАЗВИТИЯ ПЕРВИЧНОЙ ОТКРЫТОУГОЛЬНОЙ ГЛАУКОМЫ

ЗАГИДУЛЛИНА, А.Ш., АЗНАБАЕВ, Б.М., ЗУЛКАРНЕЕВ, Р.Х., ZAGIDULLINA A.SH., AZNABAEV, B.M., ZULKARNEEV, R.KH. (2022)

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