Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Sardana A. Fedorova"'
Autor:
Tuyara V. Borisova, Aleksandra M. Cherdonova, Vera G. Pshennikova, Fedor M. Teryutin, Igor V. Morozov, Alexander A. Bondar, Olga A. Baturina, Marsel R. Kabilov, Georgii P. Romanov, Aisen V. Solovyev, Sardana A. Fedorova, Nikolay A. Barashkov
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Mitochondrial forms account approximately 1–2% of all nonsyndromic cases of hearing loss (HL). One of the most common causative variants of mtDNA is the m.1555A > G variant of the MT-RNR1 gene (OMIM 561000). Currently the detection of the
Externí odkaz:
https://doaj.org/article/e857d32e5fce41179211500a006e9097
Autor:
Alena A. Nikanorova, Nikolay A. Barashkov, Vera G. Pshennikova, Fedor M. Teryutin, Sergey S. Nakhodkin, Aisen V. Solovyev, Georgii P. Romanov, Tatiana E. Burtseva, Sardana A. Fedorova
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 18, p 14052 (2023)
Thyroid hormones play a crucial role in regulating normal development, growth, and metabolic function. However, the controversy surrounding seasonal changes in free triiodothyronine (FT3) levels remains unresolved. Therefore, the aim of this study wa
Externí odkaz:
https://doaj.org/article/0cf9fd0fce0a440d8e9d12b33a2d2a27
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
Autor:
Vera G. Pshennikova, Fedor M. Teryutin, Alexandra M. Cherdonova, Tuyara V. Borisova, Aisen V. Solovyev, Georgii P. Romanov, Igor V. Morozov, Alexander A. Bondar, Olga L. Posukh, Sardana A. Fedorova, Nikolay A. Barashkov
Publikováno v:
Genes, Vol 14, Iss 5, p 1001 (2023)
The GJB2 (Cx26) gene pathogenic variants are associated with autosomal recessive deafness type 1A (DFNB1A, OMIM #220290). Direct sequencing of the GJB2 gene among 165 hearing-impaired individuals living in the Baikal Lake region of Russia identified
Externí odkaz:
https://doaj.org/article/97077420c0db4393950cd58324318976
Autor:
Alena A. Nikanorova, Nikolay A. Barashkov, Vera G. Pshennikova, Nyurgun N. Gotovtsev, Georgii P. Romanov, Aisen V. Solovyev, Sargylana S. Kuzmina, Nikolay N. Sazonov, Sardana A. Fedorova
Publikováno v:
Genes, Vol 13, Iss 9, p 1612 (2022)
Currently, it is known that irisin can participate in the processes of thermoregulation and browning of adipose tissue, and, therefore, it is possible that it is involved in the microevolutionary mechanisms of adaptation to a cold. The aim of this st
Externí odkaz:
https://doaj.org/article/4fce2e5e6e2c4d25a6dc1a993d6998ec
Autor:
Vyacheslav M. Nikolaev, Svetlana D. Efremova, Sargylana I. Sofronova, Nadezhda K. Chirikova, Sardana A. Fedorova, Anna N. Romanova
Publikováno v:
International Journal of Biomedicine, Vol 9, Iss 2, Pp 172-175 (2019)
The purpose of our research was to assess the level of tumor markers in the blood serum of elderly residents of Yakutia. Material and Methods: We examined 204 elderly residents of Yakutia (52 men aged from 60 to 74 years and 152 women aged from 55 to
Externí odkaz:
https://doaj.org/article/6f029f14491a42ebb96ec38bc1a0007d
Autor:
Georgii P. Romanov, Anna A. Smirnova, Vladimir I. Zamyatin, Aleksey M. Mukhin, Fedor V. Kazantsev, Vera G. Pshennikova, Fedor M. Teryutin, Aisen V. Solovyev, Sardana A. Fedorova, Olga L. Posukh, Sergey A. Lashin, Nikolay A. Barashkov
Publikováno v:
Biology, Vol 11, Iss 2, p 257 (2022)
An increase in the prevalence of autosomal recessive deafness 1A (DFNB1A) in populations of European descent was shown to be promoted by assortative marriages among deaf people. Assortative marriages became possible with the widespread introduction o
Externí odkaz:
https://doaj.org/article/41a5d0c6f17d44bebb1d1a79d7db13d9
Autor:
Alena A. Nikanorova, Nikolay A. Barashkov, Vera G. Pshennikova, Sergey S. Nakhodkin, Nyurgun N. Gotovtsev, Georgii P. Romanov, Aisen V. Solovyev, Sargylana S. Kuzmina, Nikolay N. Sazonov, Sardana A. Fedorova
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4657 (2021)
Leptin plays an important role in thermoregulation and is possibly associated with the microevolutionary processes of human adaptation to a cold climate. In this study, based on the Yakut population (n = 281 individuals) living in the coldest region
Externí odkaz:
https://doaj.org/article/fa57459247a44998879e720ece11b14d
Autor:
Nikolay A. Barashkov, Georgii P. Romanov, Uigulaana P. Borisova, Aisen V. Solovyev, Vera G. Pshennikova, Fedor M. Teryutin, Alexander A. Bondar, Igor V. Morozov, Elza K. Khusnutdinova, Olga L. Posukh, Tatiana E. Burtseva, Jon Øyvind Odland, Sardana A. Fedorova
Publikováno v:
International Journal of Circumpolar Health, Vol 78, Iss 1 (2019)
Waardenburg syndrome (WS) is an orphan genetic disease with autosomal dominant pattern of inheritance characterised by varying degrees of hearing loss accompanied by skin, hair and iris pigmentation abnormalities. Four types of WS differing in phenot
Externí odkaz:
https://doaj.org/article/9ce92d50cdb7413bbd9b6090097ffef5
Autor:
Sergey S. Nakhodkin, Vera G. Pshennikova, Paraskovia S. Dyachkovskaya, Nikolay A. Barashkov, Alena A. Nikanorova, Fedor M. Teryutin, Olga A. Melnichuk, Eric Crubézy, Sardana A. Fedorova, Jean-François Magnaval
Publikováno v:
International Journal of Circumpolar Health, Vol 78, Iss 1 (2019)
In 2018, a seroepidemiological survey was carried out in 3 ulus, or districts (Churapchinsky, Megino-Kangalassky and Ust-Aldansky) in Central Yakutia (Sakha Republic, Russian Federation) about 3 helminth zoonoses, namely, echinococcosis (alveolar or
Externí odkaz:
https://doaj.org/article/d91cf00708ee4a2694f8ab72b16c009d
Autor:
Vera G. Pshennikova, Nikolay A. Barashkov, Georgii P. Romanov, Fedor M. Teryutin, Aisen V. Solov’ev, Nyurgun N. Gotovtsev, Alena A. Nikanorova, Sergey S. Nakhodkin, Nikolay N. Sazonov, Igor V. Morozov, Alexander A. Bondar, Lilya U. Dzhemileva, Elza K. Khusnutdinova, Olga L. Posukh, Sardana A. Fedorova
Publikováno v:
The Scientific World Journal, Vol 2019 (2019)
In silico predictive software allows assessing the effect of amino acid substitutions on the structure or function of a protein without conducting functional studies. The accuracy of in silico pathogenicity prediction tools has not been previously as
Externí odkaz:
https://doaj.org/article/2d306a026a634d3a81ca1fcf7ceb70cb