Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Aleksandra Diakonova"'
Autor:
Nadezhda Pavlova, Aleksey Bochurov, Vladislav Alekseev, Aleksandra Diakonova, Vladimir Dodokhov, Khariton Kurtanov
Publikováno v:
International Journal of Biomedicine. 12:151-154
The aim of this study was to investigate the relationship between the HTR2A 1438A/G (rs6311) SNP and the risk of nicotine addiction in Yakuts. Methods and Results: A total of 292 people of Yakut nationality were tested (77 women and 215 men). Two gro
Autor:
Nadezhda Pavlova, Aleksey Bochurov, Vladislav Alekseev, Aleksandra Diakonova, Vladimir Dodokhov, Khariton Kurtanov
Publikováno v:
International Journal of Biomedicine. 12:155-159
Background: Genome-wide association studies identified the region of chromosome 3p21.31 as having the strongest association with the severe COVID-19 and susceptibility to SARS-CoV-2 infection. The aim of our study was to investigate the frequency of
Autor:
Aleksandra Diakonova, Nadezhda Pavlova, Vladislav Alekseev, Lyubov Mironova, Khariton Kurtanov, Vladimir Dodokhov, Innokenty Ushnitsky
Publikováno v:
International Journal of Biomedicine, Vol 11, Iss 4, Pp 576-580 (2021)
The aim of our study was to investigate the relationship between the MDR1 and MTHFR gene polymorphisms and non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Yakut population in the Republic of Sakha (Yakutia). Methods and Results:
Autor:
Dmitry A. Sychev, Vladimir V. Dodokhov, Zoya A. Rudykh, Nadezhda Pavlova, Vladislav A. Alekseev, Khariton Kurtanov, Yana V. Chertovskikh, Aleksandra Diakonova, Tuyara I. Dmitrieva, Nadezhda E. Maksimova, Lyubovy A. Sydykova
Publikováno v:
International Journal of Biomedicine, Vol 11, Iss 3, Pp 355-360 (2021)
The goal of this study was to investigate the distribution of alleles and genotypes of the KCNJ11 rs5219, PPARG rs1801282, TCF7L2 rs7903146/rs12255372 SNPs in Yakuts with T2D, in comparison with other ethnic populations. Methods and Results: The stud
Autor:
Aleksandra Diakonova, Yigulana P. Borisova, Khariton Kurtanov, Vladimir V. Dodokhov, Tuyara I. Dmitrieva, Nadezhda Pavlova, Vladislav A. Alekseev
Publikováno v:
International Journal of Biomedicine, Vol 11, Iss 3, Pp 367-371 (2021)
Background: The ABCB1 gene is responsible for resistance to various cytotoxic drugs. The product of the ABCB1 gene, P-glycoprotein (P-gp), acts as a transmembrane pump and influences the action of many drugs. More than 40 SNPs of the ABCB1 gene that
Publikováno v:
International Journal of Biomedicine, Vol 11, Iss 1, Pp 92-95 (2021)
The aim of our research was to study the distribution of alleles and genotypes of the FTO rs9939609 SNP, the PNPLA3 rs738409 SNP, and the TM6SF2 rs58542926 SNP in the Yakut population. Methods and Results: A total of 85 DNA samples from the populatio
Autor:
Khariton Kurtanov, Nadezhda Pavlova, Aleksandra Diakonova, Lyubovy Sydykova, Tuyara Aleksandrova, Yigulana Borisova, Vladimir Dodokhov
Publikováno v:
International Journal of Biomedicine. 10:433-437
Background: The first GWAS searching for such genetic factors identified the PNPLA3 gene as a major genetic determinant for the predisposition to nonalcoholic fatty liver disease in Hispanic, African American, and European American populations, accor
Autor:
Khariton Kurtanov, Nadezhda Pavlova, Aleksandra Diakonova, Lyubovy Sydykova, Sardana Markova, Vladimir Dodokhov
Publikováno v:
International Journal of Biomedicine. 10:438-441
Background: The pathogenetic mechanisms of type 2 diabetes (T2D) and non-alcoholic fatty liver disease (NAFLD) are closely related. Currently, multiple studies have demonstrated a link between the PNPLA3 148M variant and the development and progressi
Autor:
Aleksandra Diakonova, Natalia Solovyeva, Vladimir V. Dodokhov, Nadezhda Pavlova, Yigulana P. Borisova, Khariton Kurtanov, Lyubov Mironova, Innokenty Ushnitsky
Publikováno v:
International Journal of Biomedicine, Vol 10, Iss 1, Pp 50-53 (2020)
Background: The aim of this study was to search for associations between polymorphisms of the IRF6, MDR1, and MTHFR genes and the risk of congenital orofacial cleft (OFCs) among the population of the Republic of Sakha (Yakutia). Methods and Results:
Autor:
Natalia Solovyeva, Vera Yadrikinskaya, Aleksandra Diakonova, Lena Terekhova, Inna M. Mulina, Khariton Kurtanov, Tuiara Aleksandrova, Nadezhda Pavlova, Irina Solovieva
Publikováno v:
International Journal of Biomedicine, Vol 10, Iss 1, Pp 54-57 (2020)
Background: Mutations in the JAK2, CALR, and MPL genes are key factors of the classical Ph-negative CMPD pathogenesis with demonstrated diagnostic and prognostic value. The aim of this research was to study the prevalence of JAK2, CALR, and MPL mutat