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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)
of nosologies are becoming increasingly studied due to discoveries in the field of molecular biology
Достижения последних лет в пренатальной генетической диагностике малых сверхчисленных маркерных хромосом
Recent achievements in prenatal genetic diagnosis of small supernumerary marker chromosomes
Omarov, Magomed A., Mulyukov, Airat R., Burmistrov, Ivan A., Akhmadishin, Eduard I., Lapteva, Mariia S., Nizamutdinova, Adelina N., Nurieva, Kadria Z., Iagudina, Regina A., Kurbanadamov, Magomedali R., Омаров, М.А., Мулюков, А.Р., Бурмистров, И.А., Ахмадишин, Э.И., Лаптева, М.С., Низамутдинова, А.Н., Нуриева, К.З., Ягудина, Р.А., Курбанадамов, М.Р. (2024)
Recent achievements in prenatal genetic diagnosis of small supernumerary marker chromosomes
КЛИНИЧЕСКИЙ И МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ АНАЛИЗ СЛУЧАЯ СЕМЕЙНОГО РАССЕЯННОГО СКЛЕРОЗА В РЕСПУБЛИКЕ БАШКОРТОСТАН
CLINICAL AND MOLECULAR GENETIC ANALYSIS OF A CASE OF FAMILIAL MULTIPLE SCLEROSIS IN THE REPUBLIC OF BASHKORTOSTAN
Заплахова, О.В., Тимашева, Я.Р., Бахтиярова, К.З., Туктарова, И.А., Мустафина, О.Е., Zaplakhova, O.V., Timasheva, Y.R., Bakhtiyarova, K.Z., Tuktarova, I.A., Mustafina, O.E. (2019)
Objective. To investigate clinical manifestations of multiple sclerosis (MS) and the genetic makeup
Widespread natural selection on metabolite levels in humans
Timasheva, Yanina, Lepik, Kaido, Liska, Orsolya, Papp, Balázs, Kutalik, Zoltán (2024)
variants associated with traits under selection. The genetic signatures of such evolutionary events can
AVPR1A MAIN EFFECT AND OXTR-BY-ENVIRONMENT INTERPLAY IN INDIVIDUAL DIFFERENCES IN DEPRESSION LEVEL
KAZANTSEVA, A.V., DAVYDOVA, YU.D., ENIKEEVA, R.F., LOBASKOVA, M.M., MUSTAFIN, R.N., MALYKH, S.B., TAKHIROVA, Z.R., KHUSNUTDINOVA, E.K. (2020)
of genetic variants in a moderately large sample, was used. Conclusions: Our preliminary findings indicate
High-Tech Methods of Cytokine Imbalance Correction in Intervertebral Disc Degeneration
Shnayder, Natalia A., Ashhotov, Azamat V., Trefilova, Vera V., Novitsky, Maxim A., Medvedev, German V., Petrova, Marina M., Narodova, Ekaterina A., Kaskaeva, Daria S., Chumakova, Galina A., Garganeeva, Natalia P., Lareva, Natalia V., Al-Zamil, Mustafa, Asadullin, Azat R., Nasyrova, Regina F. (2023)
engineering); genetic technologies (gene modifications, microRNA, and molecular inducers of IDD); technologies
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)
molecular genetic research
ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ СИНДРОМА ДЕФИЦИТА ВНИМАНИЯ/ГИПЕРАКТИВНОСТИ. СОВРЕМЕННОЕ СОСТОЯНИЕ ПРОБЛЕМЫ
GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS OF THE PROBLEM
Р. Р. Шарафиев, R. R. Sharafiev, А. Р. Асадуллин, A. R. Asadullin, В. Л. Юлдашев, V. L. Yuldashev, А. В. Анцыборов, A. V. Antsyborov, Л. В. Лямина, L. V. Lyamina, Э. А. Ахметова, E. A. Akhmetova (Медицинский вестник Башкортостана, №4, 2018)
GENETIC PECULIARITIES OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD). UPDATE STATUS
Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant
Elena, Merkuryeva, Tatiana, Markova, Anton, Tyurin, Diana, Valeeva, Vladimir, Kenis, Maria, Sumina, Igor, Sorokin, Olga, Shchagina, Mikhail, Skoblov, Maria, Nefedova, Rita, Khusainova, Ekaterina, Zakharova, Dadali, Elena, Kutsev, Sergey (2023)
of this variant will contribute to optimal molecular genetic diagnostics, which can reduce diagnostic costs
Exosomal non coding RNAs as a novel target for diabetes mellitus and its complications
Sufianov, A., Kostin, A., Begliarzade, S., Kudriashov, V., Ilyasova, T., Liang, Y., Mukhamedzyanov, A., Beylerli, O. (2023)
of the molecular genetic mechanisms of the pathogenesis of DM is of critical importance for the development of new

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