Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Nikolay A, Barashkov"'
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
Autor:
Leonid A. Klarov, Vera G. Pshennikova, Georgii P. Romanov, Aleksandra M. Cherdonova, Aisen V. Solovyev, Fedor M. Teryutin, Nikolay V. Luginov, Petr M. Kotlyarov, Nikolay A. Barashkov
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 23, p 15372 (2022)
Pathogenic variants in the SLC26A4, FOXI1, and KCNJ10 genes are associated with hearing loss (HL) and specific inner ear abnormalities (DFNB4). In the present study, phenotype analyses, including clinical data collection, computed tomography (CT), an
Externí odkaz:
https://doaj.org/article/9fc62f8a873c416391e6850d1596cb4d
Autor:
Sardana Kononova, Dekabrina Vinokurova, Nikolay A Barashkov, Ariadna Semenova, Sargylana Sofronova, Sidorova Oksana, Davydova Tatiana, Valentin Struchkov, Tatiana Burtseva, Anna Romanova, Sardana Fedorova
Publikováno v:
International Journal of Circumpolar Health, Vol 80, Iss 1 (2021)
This pilot research was one of the first sociological studies with general questions on genetic testing with 300 participants, 75% of which were representatives of one people – the Sakha. A quantitative method was used: a sociological survey with q
Externí odkaz:
https://doaj.org/article/197b8d8cf6ca43deb1a56d02327561c4
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:
Georgii P Romanov, Vera G Pshennikova, Sergey A Lashin, Aisen V Solovyev, Fedor M Teryutin, Aleksandra M Cherdonova, Tuyara V Borisova, Nikolay N Sazonov, Elza K Khusnutdinova, Olga L Posukh, Sardana A Fedorova, Nikolay A Barashkov
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0242219 (2020)
The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the dis
Externí odkaz:
https://doaj.org/article/1fad53822f4a4f9f985e33c6a373c125
Autor:
Marina V. Zytsar, Nikolay A. Barashkov, Marita S. Bady-Khoo, Olga A. Shubina-Olejnik, Nina G. Danilenko, Alexander A. Bondar, Igor V. Morozov, Aisen V. Solovyev, Valeriia Yu. Danilchenko, Vladimir N. Maximov, Olga L. Posukh
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations of Caucasian origin. Data on the c.35de
Externí odkaz:
https://doaj.org/article/b6738adfe8d943aa907dab8a1b0ae287
Autor:
Valeriia Yu. Danilchenko, Marina V. Zytsar, Ekaterina A. Maslova, Marita S. Bady-Khoo, Nikolay A. Barashkov, Igor V. Morozov, Alexander A. Bondar, Olga L. Posukh
Publikováno v:
Diagnostics, Vol 11, Iss 12, p 2378 (2021)
Hereditary hearing loss (HL) is known to be highly locus/allelic heterogeneous, and the prevalence of different HL forms significantly varies among populations worldwide. Investigation of region-specific landscapes of hereditary HL is important for l
Externí odkaz:
https://doaj.org/article/4800eab104624524956d659e19c4d0b7
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