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Role of Retroelements in Frontotemporal Dementia Development
Mustafin, Rustam Nailevich (2025)
are found. Therefore, genetic predisposition to FTD may influence the interaction between retroelements
Генетические модификации в кардиологии: роль CRISPR-Cas9 в терапии сердечно-сосудистых заболеваний
Genetic modifications in cardiology: the role of CRISPR-Cas9 in the treatment of cardiovascular diseases
Gretseva, Tatyana A., Enikeyev, Damir A., Shaidullina, Evelina A., Djanbekova, Liana M., Karpelevich, Valeria S., Kuzhina, Alsu R., Magomedova, Alleiss I., Valeev, Ildar R., Gimranova, Gulnaz S., Sayarova, Leysan M., Klavdieva, Nadezhda A., Ataeva, Aminat A., Salimova, Natali Yu., Menyasheva, Diana R., Berdiev, Bakhrom M., Грецева, Т.А., Еникеев, Д.А., Шайдуллина, Э.А., Джанбекова, Л.М., Карпелевич, В.С., Кужина, А.Р., Магомедова, А.И., Валеев, И.Р., Гимранова, Г.С., Саярова, Л.М., Клавдиева, Н.А., Атаева, А.А., Салимова, Н.Ю., Меняшева, Д.Р., Бердиев, Б.М. (2025)
Genetic modifications in cardiology: the role of CRISPR-Cas9 in the treatment of cardiovascular
Evaluation of Polygenic Risk Score for Prediction of Childhood Onset and Severity of Asthma
Savelieva, Olga, Karunas, Alexandra, Prokopenko, Inga, Balkhiyarova, Zhanna, Gilyazova, Irina, Khidiyatova, Irina, Khusnutdinova, Elza (2025)
Asthma is a common complex disease with susceptibility defined through an interplay of genetic
Лихеноидный парапсориаз: современные представления о патогенезе и факторах риска
Pityriasis lichenoides: Modern ideas about pathogenesis and risk factors
Sultanova, Elvira A., Dvoriankova, Evgeniya V., Khismatullina, Zarema R., Султанова, Э. А., Дворянкова, Е. В., Хисматуллина, З. Р. (2025)
Relationship of MicroRNAs to Transposons in Osteoarthritis Development
Mustafin, R.N., Khusnutdinova, E.K. (2025)
of the disease is associated with an impact on genes and signaling pathways regulating cell proliferation
Alu Polymorphisms of Autophagy and Apoptosis Regulatory Genes as Human Lifespan Factors
Erdman, V.V., Karimov, D.D., Tuktarova, I.A., Petintseva, A.A., Timasheva, Y.R., Nasibullin, T.R. (2025)
of the SEMA6A (Yb8NBC597*ID, HR = 0.54, P = 0.016 for the cerebrovascular diseases), TEAD1 (Ya5ac2013*II, HR
ANALYSIS OF CLINICAL MANIFESTATIONS OF NEUROFIBROMATOSIS TYPE 1 IN PATIENTS WITH NONSENSE PATHOGENIC VARIANTS IN THE NF1 GENE FROM THE REPUBLIC OF BASHKORTOSTAN
Mustafin, R.N., Bermisheva, M.A., Karunas, A.S., Akhmetshin, A.A., Monakhova, A.S., Khusnutdinova, E.K. (2025)
of the genetic causes of NF1 can become the basis for prenatal diagnosis and the use of new methods of treating
ABERRANT METHYLATION GENES MIR-663A AND MIR-663B AND OVARIAN CANCER PATHOGENESIS
Fedorova, Yu. Yu., Aminova, E.T., Faishanova, R.R., Zagitov, I.R., Romanova, A.R., Nurgalieva, A.Kh., Andreeva, E.A., Darvish, M., Khusnutdinova, E.K., Prokofyeva, D.S. (2025)
worldwide. As is known, the course of ovarian cancer depends on many factors, including genetic
The role of pathogenic germline mutations of BRCA1/2, NBS1, and CHEK2 genes in gastric cancer development within the Volga-Ural region of Russia
Nurgalieva, A.Kh., Petrova, Sabina G., Gallyamova, Lilia F., Ekomasova, Natalia V., Sakaeva, Dina D., Fedorova, Yulia Yu, Dzhaubermezov, Murat A., Abdeev, Rustem R., Rakhimov, Radmir R., Khusnutdinova, Elza K., Prokofyeva, Darya S. (2025)
high mortality rate. Hereditary predisposition to GC is still not fully understood. The objective
Поиск ассоциации полиморфных локусов генов HIF1A, VEGFA с риском развития рака яичников у женщин Республики Башкортостан
STUDY OF THE ASSOCIATION BETWEEN HIF1A AND VEGFA GENE POLYMORPHISMS AND OVARIAN CANCER RISK IN WOMEN FROM BASHKORTOSTAN
Андреева, Е. А., Аминова, Э. Т., Фаисханова, Р. Р., Загитов, И. Р., Валова, Я. В., Федорова, Ю. Ю., Нургалиева, А. Х., Дарвиш, М., Сакаева, Д. Д., Хуснутдинова, Э. К., Прокофьева, Д. С., Andreeva, E.A., Aminova, E.T., Faiskhanova, R.R., Zagitov, I.R., Valova, Y.V., Fedorova, Yu.Yu., Nurgalieva, A.Kh., Darvish, M., Sakaeva, D.D., Khusnutdinova, E.K., Prokofyeva, D.S. (2025)
genetic polymorphisms

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