По вашему запросу найдено документов: 580

Страница 9 из 58

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
ГЕННАЯ ТЕРАПИЯ: РИСКИ И ПРЕИМУЩЕСТВА
GENE THERAPIES: RISK AND BENEFITS
Янбердина, К.И., Сад, А.С., Yanberdina, K.I., Sad, A.S. (2024)
genetic engineering
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
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
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
Benefits of Using the CRISPR/Cas9 System for the Correction of Genetic Mutations
Sharipov, R.A., Omarov, M.A., Mulyukov, A.R., Dybova, A.I., Vyaseleva, E.T., Kayumova, N.B., Saitgalina, A. Sh., Ententeev, K.R., Iagafarov, I.R., Kuserbaev, I.V., Gubaeva, E.A. (2023)
and genetics. However, the application of the CRISPR/Cas9 technology has some limitations and difficulties
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
СОВРЕМЕННЫЕ СВЕДЕНИЯ О ГЕНЕТИЧЕСКОЙ НЕОДНОРОДНОСТИ ВРОЖДЕННЫХ КАТАРАКТ
CURRENT INFORMATION ON GENETIC HETEROGENEITY OF CONGENITAL CATARACTS
Корсакова, Н.В., Белкова, Т.А., Korsakova, N.V., Belkova, T.A. (2020)
CURRENT INFORMATION ON GENETIC HETEROGENEITY OF CONGENITAL CATARACTS
ПРЕДИКТОРЫ ОККЛЮЗИОННЫХ НАРУШЕНИЙ ПО ДАННЫМ ТЕЛЕРЕНТГЕНОГРАФИИ
PREDICTORS OF OCCLUSIVE DISORDERS ACCORDING TO TELERENTGENOGRAPHY
ДЕВЯТИРИКОВ, Д.А., ПУТАЛОВА, И.Н., СУСЛО, А.П., СЛАВНОВ, А.А., ШИРОЧЕНКО, С.Н., ГРИНЕНКО, О.В., СИДЕНКО, Н.И., Devyatirikov, D.A., Putalova, I.N., Suslo, A.P., Slavnov, A.A., Shirochenko, S.N., Grinenko, O.V., Sidenko, N.I. (2024)
PREDICTORS OF OCCLUSIVE DISORDERS ACCORDING TO TELERENTGENOGRAPHY

Страница 9 из 58

Google Scholar
OpenDoar

Фасеты

Научный руководитель
Авторы
Ключевые слова
Год