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По вашему запросу найдено документов: 462

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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

Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078))

Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial

Mendelian Randomization Analysis Identifies Inverse Causal Relationship between External Eating and Metabolic Phenotypes

Timasheva, Yanina, Balkhiyarova, Zhanna, Avzaletdinova, Diana, Morugova, Tatyana, Korytina, Gulnaz F., Nouwen, Arie, Prokopenko, Inga, Kochetova, Olga (2024)

phenotypes remain unclear. We aimed to identify genetic variants linked to eating behaviour and investigate

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