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Роль мутаций в гене NF1 в спорадическом канцерогенезе
The role of mutations in NF1 gene in sporadic carcinogenesis
Мустафин, Р. Н., Mustafin, R.N. (2021)
The review article presents data on somatic inactivation of NF1 gene as a cause of sporadic
ГЕННАЯ ТЕРАПИЯ: РИСКИ И ПРЕИМУЩЕСТВА
GENE THERAPIES: RISK AND BENEFITS
Янбердина, К.И., Сад, А.С., Yanberdina, K.I., Sad, A.S. (2024)
GENE THERAPIES: RISK AND BENEFITS
ROLE OF ALLELIC GENES OF MATRIX METALLOPROTEINASES AND THEIR TISSUE INHIBITORS IN THE RISK OF PEPTIC ULCER DISEASE DEVELOPMENT
Shaymardanova, E.Kh., Nurgalieva, A.Kh., Khidiyatova, I.M., Gabbasova, L.V., Kuramshina, O.A., Kryukova, A.Ya., Sagitov, R.B., Munasipov, F.R., Khusnutdinova, E.Kh. (2016)
of the stomach and/or duodenum. Association analysis of common polymorphisms of matrix metalloproteinases genes
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)
with osteogenesis imperfecta. The disease is caused by pathogenic variants in the SGMS2 gene, the protein product
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)
2, CDH4, SEMA6A, PKHD1L1, STK38L, HECW1, and TEAD1 genes, which are candidates of aging
INVESTIGATION OF THE ROLE OF CYTOKINE GENES POLYMORPHISMS IN THE DEVELOPMENT OF THE URTICARIA IN THE REPUBLIC OF BASHKORTOSTAN
Gimalova, G.K., Karunas, A.S., Khusuntdinova, E.K., Khantimerova, E.F., Zagidullin, S.Z. (2017)
of interleukins genes IL4 (rs2243250), IL4R (rs1805010), IL10 (rs1800872), IL13 (rs20541) and tumor necrosis
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga–Ural Region
Khidiyatova, Irina, Khidiyatova, Indira, Zinchenko, Rena, Marakhonov, Andrey, Karunas, Alexandra, Avkhadeeva, Svetlana, Aznzbaev, Marat, Khusnutdinova, Elza (2023)
and frequencies of mutations in the responsible genes, and examine clinical and genetic correlations. Based
Polygenic Analysis of Cytokine and Inflammatory Gene Polymorphisms in Chronic Obstructive Pulmonary Disease
Korytina, G.F., Aznabaeva, Y.G., Kochetova, O.V., Nasibullin, T.R., Akhmadishina, L.Z., Khusnutdinova, N.N., Zagidullin, N. Sh., Victorova, T.V. (2023)
the association of cytokines and inflammatory genes polymorphisms and their combinations with COPD. SNPs
Germline Variants in Proto-Oncogenes and Tumor Suppressor Genes in Women with Cervical Cancer
Lenkova, Ksenia, Khusainova, Rita, Minyazeva, Raushaniya, Zaripova, Aliya, Gilyazova, Irina, Mokrysheva, Natalia, Minniakhmetov, Ildar (2024)
pathogenesis. This study aimed to investigate germline variants in proto-oncogenes and tumor suppressor genes
АНАЛИЗ АССОЦИАЦИЙ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНОВ АМИНОКСИДАЗЫ 1 AOC1 И ГИСТАМИН-N-МЕТИЛТРАНСФЕРАЗЫ HNMT С РАЗВИТИЕМ БРОНХИАЛЬНОЙ АСТМЫ У ДЕТЕЙ
Association analysis of amine oxidase 1 AOC1 and histamine-N-methyl-transferase HNMT genes polymorphism with the development of asthma in children
Savelyeva, O.N., Karunas, A.S., Fedorov, Y.Y., Gatiyatullin, R.F., Etkina, E.I., Khusnutdinova, E.K., Савельева, О.Н., Карунас, А.С., Федорова, Ю.Ю., Гатиятуллин, Р.Ф., Эткина, Э.И., Хуснутдинова, Э.К. (2020)
-N-methyltransferase HNMT genes, involved in histamine metabolism, with predicting the risk of developing bronchial asthma

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