По вашему запросу найдено документов: 13

Страница 1 из 2

Novel Genetic Risk Marker for Paranoid Schizophrenia in the Chromosomal Region 9q21.13 in Tatars: A Genome-Wide Association Analysis
Gareeva, A.E. (2024)
with paranoid schizophrenia and 383 healthy individuals of Tatar ethnicity. As a result of the study
Searching for Ethnospecific Risk Markers of Paranoid Schizophrenia in Bashkirs Based on the Results from Genome-Wide Association Study
Gareeva, A.E. (2024)
ethnicity
Genome-Wide Analysis of the Risk Association for the Development of Paranoid Schizophrenia in Russians: Search for Genetic Markers in the 1q43 Chromosomal Region
Gareeva, A.E. (2024)
ethnicity
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)
regulator gene (CFTR) mutations in the population, which is determined by genetic diversity and ethnicity
The Genetic Markers of Knee Osteoarthritis in Women from Russia
Tyurin, Anton, Akhiiarova, Karina, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)
to the clinical and ethnic heterogeneity of the studied populations. To find the genetic markers
Hypomethylation of the RUNX2 Gene Is a New Potential Biomarker of Primary Osteoporosis in Men and Women
Yalaev, Bulat, Tyurin, Anton, Akhiiarova, Karina, Khusainova, Rita (2024)
years of age of Russian ethnicity from the Volga-Ural region of Russia was carried out. The level of DNA
СИНДРОМ МЮНХМЕЙЕРА: ГЕНЕТИЧЕСКИЕ МЕХАНИЗМЫ, ТЕХНОЛОГИИ ДИАГНОСТИКИ И ЛЕЧЕНИЯ
MUNCHMEYER SYNDROME: GENETIC MECHANISMS, DIAGNOSTIC AND TREATMENT TECHNOLOGIES
Батыршин, А. А., Batyrshin, A.A. (2024)
Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases
Savelieva, O.N., Karunas, A.S., Biktasheva, A.R., Vlasova, A.O., Khidiyatova, I.M., Etkina, E.I., Khusnutdinova, E.K. (2024)
of Bashkortostan. DNA samples of 358 individuals with allergic airway diseases of different ethnicity (Russians—165
The frequent variant A57F in the GNE gene in patients from Russia has Finno-Ugric Mari origin
Subbotin, Dmitrii, Ionova, Sofya, Marakhonov, Andrey, Saifullina, Elena, Borovikov, Artem, Akhmadeeva, Leila, Chausova, Polina, Ryzhkova, Oksana, Zinchenko, Rena, Kutsev, Sergey, Murtazina, Aysylu (2024)
_170delinsTT (p.(Ala57Phe)) variant in the GNE gene (NM_001128227.3) among different ethnic populations (Mari
Myopic Macular Atrophy in the Two-Continent Population-Based Study
Jonas, Jost B., Bikbov, Mukharram M., Kazakbaeva, Gyulli M., Wang, Ya Xing, Xu, Jie, Jonas, Rahul A., Panda-Jonas, Songhomitra (2024)
) and myopic patchy atrophies (MMD stage 3) in three ethnically different cohorts recruited in a population

Страница 1 из 2

Google Scholar
OpenDoar

Фасеты

Научный руководитель
Авторы
Ключевые слова
Год