По вашему запросу найдено документов: 90

Страница 1 из 9

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
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
MULTILOCUS ASSOCIATIONS OF INFLAMMATORY GENES WITH THE RISK OF TYPE 1 DIABETES
TIMASHEVA, Y.R., NASIBULLIN, T.R., MUSTAFINA, O.E., BALKHIYAROVA, Z.R., PROKOPENKO, I., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
Background Genome-wide association studies have captured a large proportion of genetic variation
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
IN SEARCH FOR GENETIC MARKERS OF NON-FAMILIA SICK SINUS SYNDROME
Zagidullin, N., Plechev, V., Badykova, E., Badykov, M., Akhmadishina, L., Korytina, G., Sagitov, I. (2019)
Background Sick sinus syndrome (SSS) can result from genetic and environmental factors. More than a
ASSOCIATION OF VARIABLE RS1801282 LOCUS OF PPARG2 GENE WITH DIABETIC NEPHROPATHY
Avzaletdinova, D.Sh., Sharipova, L.F., Kochetova, O.V., Morugova, T.V., Erdman, V.V., Mustafina, O.E. (2016)
genetic predisposition
GENETIC DETERMINANTS OF ESSENTIAL HYPERTENSION IN THE POPULATION OF TATARS FROM RUSSIA
Timasheva, Y., Nasibullin, T., Imaeva, E., Mirsaeva, G., Mustafina, O. (2016)
is characterized by a unique combination of European and Asian genetic ancestry, and is an interesting object
The role of genetic factors in levodopa-induced dyskinesias development in Russian patients with Parkinson's disease: A pilot study
Akhmadeeva, G., Khidiyatova, I., Gilyazova, I., Baitimerov, A., Magzhanov, R. (2019)
The role of genetic factors in levodopa-induced dyskinesias development in Russian patients
MicroRNA Processing Pathway-Based Polygenic Score for Clear Cell Renal Cell Carcinoma in the Volga-Ural Region Populations of Eurasian Continent
Ivanova, E., Gilyazova, I., Pavlov, V., Izmailov, A., Gimalova, G., Karunas, A., Prokopenko, I., Khusnutdinova, E. (2022)
individuals without the disease. Individual genetic risks were defined using the SNP-variant effects derived

Страница 1 из 9

Google Scholar
OpenDoar

Фасеты

Авторы
Ключевые слова
Год