Zobrazeno 1 - 10 of 235 pro vyhledávání: '"Karunas A"'
1
Akademický článek
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga–Ural Region
Autor: Irina Khidiyatova, Indira Khidiyatova, Rena Zinchenko, Andrey Marakhonov, Alexandra Karunas, Svetlana Avkhadeeva, Marat Aznzbaev, Elza Khusnutdinova
Publikováno v: Current Issues in Molecular Biology, Vol 45, Iss 6, Pp 5145-5163 (2023)
Hereditary cataracts are characterized by significant clinical and genetic heterogeneity, which can pose challenges for early DNA diagnosis. To comprehensively address this problem, it is essential to investigate the epidemiology of the disease, perf
Externí odkaz: https://doaj.org/article/e23b57bc8ee841fe80fc83f9161d2b5a
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2
Akademický článek
COVID-19: Mechanisms, risk factors, genetics, non-coding RNAs and neurologic impairments
Autor: Irina Gilyazova, Yanina Timasheva, Alexandra Karunas, Anastasiya Kazantseva, Albert Sufianov, Andrey Mashkin, Gulnaz Korytina, Yaolou Wang, Ilgiz Gareev, Elza Khusnutdinova
Publikováno v: Non-coding RNA Research, Vol 8, Iss 2, Pp 240-254 (2023)
The novel coronavirus infection (COVID-19) causes a severe acute illness with the development of respiratory distress syndrome in some cases. COVID-19 is a global problem of mankind to this day. Among its most important aspects that require in-depth
Externí odkaz: https://doaj.org/article/3b576b3a37c448a9939d6992f8d60284
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3
Akademický článek
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4
Akademický článek
MicroRNA Expression Signatures in Clear Cell Renal Cell Carcinoma: High-Throughput Searching for Key miRNA Markers in Patients from the Volga-Ural Region of Eurasian Continent
Autor: Irina Gilyazova, Elizaveta Ivanova, Adel Izmailov, Ildar Sharifgaliev, Alexandra Karunas, Elena Pudova, Anastasiya Kobelyatskaya, Gulshat Gilyazova, Angelina Izmailova, Valentin Pavlov, Elza Khusnutdinova
Publikováno v: International Journal of Molecular Sciences, Vol 24, Iss 8, p 6909 (2023)
Clear cell renal cell carcinoma (ccRCC) is characterized by high molecular genetic heterogeneity, metastatic activity and unfavorable prognosis. MicroRNAs (miRNA) are 22-nucleotide noncoding RNAs that are aberrantly expressed in cancer cells and have
Externí odkaz: https://doaj.org/article/eb41b8838f494463a35c7a32ab5cc76a
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5
Akademický článek
The role of polymorphic variants of arginase genes (ARG1, ARG2) involved in beta-2-agonist metabolism in the development and course of asthma
Autor: O. N. Savelieva, A. S. Karunas, Yu. Yu. Fedorova, R. R. Murzina, A. N. Savelieva, R. F. Gatiyatullin, E. I. Etkina, E. K. Khusnutdinova
Publikováno v: Вавиловский журнал генетики и селекции, Vol 24, Iss 4, Pp 391-398 (2020)
Asthma is a common severe disease of the respiratory tract, it leads to a significant impairment in the quality of a patient’s life unless effectively treated. Uncontrolled asthma symptoms are a cause of disease progression and development, they le
Externí odkaz: https://doaj.org/article/805344f6e67f45ac9d52fad540c81bcf
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6
Akademický článek
Using a Polygenic Score to Predict the Risk of Developing Primary Osteoporosis
Autor: Bulat Yalaev, Anton Tyurin, Inga Prokopenko, Aleksandra Karunas, Elza Khusnutdinova, Rita Khusainova
Publikováno v: International Journal of Molecular Sciences, Vol 23, Iss 17, p 10021 (2022)
Osteoporosis (OP) is a multifactorial bone disease belonging to the metabolic osteopathies group. Using the polygenic score (PGS) approach, we combined the effects of bone mineral density (BMD) DNA loci, affecting osteoporosis pathogenesis, based on
Externí odkaz: https://doaj.org/article/9ae9643dbd984a7aab985a0c1ce7b39f
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8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
10
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga–Ural Region
Autor: Khusnutdinova, Irina Khidiyatova, Indira Khidiyatova, Rena Zinchenko, Andrey Marakhonov, Alexandra Karunas, Svetlana Avkhadeeva, Marat Aznzbaev, Elza
Publikováno v: Current Issues in Molecular Biology; Volume 45; Issue 6; Pages: 5145-5163
Hereditary cataracts are characterized by significant clinical and genetic heterogeneity, which can pose challenges for early DNA diagnosis. To comprehensively address this problem, it is essential to investigate the epidemiology of the disease, perf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=multidiscipl::87efce1b16058bf658fb698c9ed016ea
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