Zobrazeno 1 - 10
of 81
pro vyhledávání: '"A S, Karunas"'
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
Autor:
I. M. Khidiyatova, E. V. Saifullina, A. S. Karunas, A. F. Akhmetgaleyeva, R. F. Kutlubaeva, L. A. Smakova, S. L. Lobov, A. V. Polyakov, O. A. Shchagina, V. A. Kadnikova, O. P. Ryzhkova, R. V. Magzhanov, E. K. Khusnutdinova
Publikováno v:
Russian Journal of Genetics. 58:1145-1153
Autor:
Olga N. Savelieva, Aleksandra S. Karunas, Yuliya Yu. Fedorova, Radik F. Gatiyatullin, Esfir I. Etkina, Elza K. Khusnutdinova
Publikováno v:
PULMONOLOGIYA. 31:729-738
Asthma is a common multifactorial disease characterized by chronic inflammation of the respiratory tract. Insufficient control of asthma symptoms significantly reduces the patient’s quality of life, leads to the risk for more severe disease and dis
Publikováno v:
Biochemical Genetics. 59:1527-1543
The GSDMB gene encodes gasdermin B from the family of gasdermin domain-containing proteins involved in various cellular processes related to tumor development and progression, such as differentiation, cell cycle control and apoptosis. Previously, we
Autor:
N. R. Ryabchikova, I. R. Minniakhmetov, G. Sh. Safuanova, D. V. Islamgulov, A. S. Karunas, E. E. Khusnutdinova
Publikováno v:
Онкогематология, Vol 8, Iss 1, Pp 7-16 (2014)
Use of tyrosine kinase inhibitor imatinib has led to significant progress in chronic myeloid leukemia (CML) treatment. To date, genetic monitoring is a mandatory attribute of therapy with tyrosine kinase inhibitors. The purpose of this study was to a
Externí odkaz:
https://doaj.org/article/a78e68cbe8f34888a2250b69aeab33c0
Autor:
A. S. Karunas, E. I. Etkina, A. N. Savelieva, R. R. Murzina, O. N. Savelieva, R. F. Gatiyatullin, Elza Khusnutdinova, Yu. Yu. Fedorova
Publikováno v:
Vavilov Journal of Genetics and Breeding. 24:391-398
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
Autor:
O. A. Shchagina, A. S. Karunas, N. V. Vyalova, G. M. Bayazutdinova, A. A. Sokolov, A. V. Polyakov
Publikováno v:
Russian Journal of Genetics. 55:1528-1535
Wilson’s disease (WD) is an autosomal recessive disease caused by an excessive accumulation of copper. The molecular genetic etiology of the disease is due to impairment of the ATP7B gene encoding copper-transporting ATPase. The spectrum and freque
Autor:
O. N. Savelieva, R. R. Murzina, A. S. Karunas, Yu. Yu. Fedorova, G. F. Gimalova, E. K. Khusnutdinova, R. F. Gatiyatullin, E. I. Etkina
Publikováno v:
Russian Journal of Genetics. 55:1520-1527
Bronchial asthma (BA) is a common severe and disabling multifactorial disease. Up to 50–60% of differences in sensitivity to therapy in patients with BA is due to genetic variability. We studied polymorphic variants of four genes involved in the me
Autor:
R. N. Mustafin, A. Kazantseva, A. S. Karunas, R. F. Enikeeva, E. K. Khusnutdinova, Sergey Malykh, Yu. D. Davydova
Publikováno v:
Russian Journal of Genetics. 55:1051-1060
Multiple studies demonstrating the association of aggressive behavior with allelic variants of neurotransmitter system genes appear to be controversial, while “risk” alleles have no effect on impaired gene expression and functioning of encoded pr
Autor:
Elza Khusnutdinova, A. S. Malykh, Sergey Malykh, A. S. Karunas, R. F. Enikeeva, Yulia Davydova
Publikováno v:
Russian Journal of Genetics. 55:783-793
The paper presents a review of the results of molecular genetic studies of cognitive abilities. To date, a small number of genes responsible for normal cognitive functioning have been detected despite numerous studies based on the approach of candida