Zobrazeno 1 - 10
of 63
pro vyhledávání: '"L. Z. Akhmadishina"'
Autor:
G. F. Korytina, L. Z. Akhmadishina, V. A. Markelov, Y. G. Aznabaeva, O. V. Kochetova, T. R. Nasibullin, A. P. Larkina, N. N. Khusnutdinova, N. Sh. Zagidullin, T. V. Victorova
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 27, Iss 5, Pp 512-521 (2023)
Chronic obstructive pulmonary disease (COPD) is a multifactorial disease of the respiratory system which develops as a result of a complex interaction of genetic and environmental factors closely related to lifestyle. We aimed to assess the combined
Externí odkaz:
https://doaj.org/article/e98b82b40a7146d4aee8b68fa40b0514
Publikováno v:
Медицинская иммунология, Vol 20, Iss 5, Pp 739-746 (2018)
In the present study, we have investigated frequency of genotypes and functional alleles of genes encoding chemokines (CXCL12 rs1801157, CCL2 rs1024611), chemokine receptors (CCR5 del32, CX3CR1 rs3732378), acute phase proteins SAA rs1136743, and CD14
Externí odkaz:
https://doaj.org/article/8892f359b488490c9c9a03392285ec01
Publikováno v:
European Respiratory Review, Vol 15, Iss 101, Pp 230-232 (2006)
Chronic obstructive pulmonary disease (COPD) is a complex heterogeneous respiratory disease. COPD is characterized by a progressive irreversible airflow limitation that is due to a loss of lung elasticity resulting from peripheral airflow obstruction
Externí odkaz:
https://doaj.org/article/4d400554856748be91675e88dc012b2b
Autor:
S. M. Izmaǐlova, L. Z. Akhmadishina, Sh. R. Zulkarneev, T. V. Victorova, Sh. Z. Zagidullin, O. V. Kochetova, Timur R. Nasibullin, Gulnaz F. Korytina, Yu. G. Aznabaeva
Publikováno v:
Russian Journal of Genetics. 57:1294-1303
Autor:
Viktorova Tv, Naufal Sh. Zagidullin, Shamil Zagidullin, Timur R. Nasibullin, L. Z. Akhmadishina, O. V. Kochetova, Gulnaz F. Korytina, Yulia G. Aznabaeva
Publikováno v:
Biochemical Genetics. 60:54-79
Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory lung disease affecting primarily distal respiratory pathways and lung parenchyma. This study aimed to determine possible genetic association of chemokine and chemokine receptor ge
Autor:
Timur R. Nasibullin, Vladimir V. Plechev, Ildus Sagitov, Yanina Timasheva, L. Z. Akhmadishina, Marat Rifkatovich Badykov, Elena Badykova, Naufal Zagidullin, Alfiya Pushkareva
Publikováno v:
Molecular Biology Reports. 48:5355-5362
Sick sinus syndrome (SSS) encompasses a group of conduction disorders characterized by the inability of sinoatrial node to perform its pacemaker function. Our aim was to identify genetic predictors of SSS in a prospective cohort of patients admitted
Autor:
Gulnaz F. Korytina, V. V. Victorov, D. S. Avzaletdinova, L. Z. Akhmadishina, T. V. Victorova, Z. A. Shangareeva, O. V. Kochetova
Publikováno v:
Russian Journal of Genetics. 57:598-606
Obesity and related complications are caused by eating disorders. The complex pathogenesis of the formation of food dependence has a genetic basis. This paper investigates the relationship between polymorphic variants of genes coding for glutamate re
Autor:
S. M. Izmailova, Yu. G. Aznabaeva, O. V. Kochetova, Sh. Z. Zagidullin, T. V. Victorova, Gulnaz F. Korytina, L. Z. Akhmadishina
Publikováno v:
Russian Journal of Genetics. 56:972-981
The aim of the present study was to investigate the association of COPD and frequent exacerbator COPD phenotype with CRP, CD14, and pro-inflammatory cytokines and their receptors (TNFA, LTA, TNFRSF1A, TNFRSF1B, IL1B, and IL6) genes. It was found that
Autor:
L. Z. Akhmadishina, I. R. Gilyazova, G. F. Zinnatullina, E. K. Khusnutdinova, Marina Bermisheva, G. F. Gimalova
Publikováno v:
Russian Journal of Genetics. 55:899-903
WRN/RECQL2 plays a crucial role in DNA replication and the maintenance of genome stability. Inactivating mutations in RECQL2 lead to Werner syndrome, a rare autosomal recessive chromosomal disorder characterized by premature aging and associated with
Autor:
Olga E. Mustafina, L. Z. Akhmadishina, L. F. Sharipova, T. V. Morugova, O. V. Kochetova, Gulnaz F. Korytina, D. S. Avzaletdinova
Publikováno v:
Russian Journal of Genetics. 55:495-503
Diabetes mellitus is a hereditary predisposed multifactorial disease. However, the genetic mechanisms of its development have not been fully revealed yet. We conducted a search for associations of polymorphic variants of the LEPR (rs1137100), LRP5 (r