Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Nikolay A Barashkov"'
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, 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:
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:
Nikolay A Barashkov, Vera G Pshennikova, Olga L Posukh, Fedor M Teryutin, Aisen V Solovyev, Leonid A Klarov, Georgii P Romanov, Nyurgun N Gotovtsev, Andrey A Kozhevnikov, Elena V Kirillina, Oksana G Sidorova, Lena M Vasilyevа, Elvira E Fedotova, Igor V Morozov, Alexander A Bondar, Natalya A Solovyevа, Sardana K Kononova, Adyum M Rafailov, Nikolay N Sazonov, Anatoliy N Alekseev, Mikhail I Tomsky, Lilya U Dzhemileva, Elza K Khusnutdinova, Sardana A Fedorova
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0156300 (2016)
Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause of hearing impairment (HI). More than 300 allelic variants have been identified in the GJB2 gene. Spectrum and allelic frequencies of the GJB2 gene vary signifi
Externí odkaz:
https://doaj.org/article/f81ef01b7f9f4787a28282561df238bc
Autor:
Nikolay A Barashkov, Fedor M Teryutin, Vera G Pshennikova, Aisen V Solovyev, Leonid A Klarov, Natalya A Solovyeva, Andrei A Kozhevnikov, Lena M Vasilyeva, Elvira E Fedotova, Maria V Pak, Sargylana N Lekhanova, Elena V Zakharova, Kyunney E Savvinova, Nyurgun N Gotovtsev, Adyum M Rafailo, Nikolay V Luginov, Anatoliy N Alexeev, Olga L Posukh, Lilya U Dzhemileva, Elza K Khusnutdinova, Sardana A Fedorova
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100848 (2014)
Age-Related Hearing Impairment (ARHI) is one of the frequent sensory disorders registered in 50% of individuals over 80 years. ARHI is a multifactorial disorder due to environmental and poor-known genetic components. In this study, we present the dat
Externí odkaz:
https://doaj.org/article/81ddea6820c846f3858073e257a4b365
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
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; Volume 14; Issue 5; Pages: 1001
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
Autor:
Alena Nikanorova, Sergey Nakhodkin, Anastasiya Kazantseva, Sardana Fedorova, Vera Pshennikova, Nikolay A Barashkov, Elza Khusnutdinova
Publikováno v:
Yakut Medical Journal. :112-116
Autor:
V.G. Pshennikova, Olga L. Posukh, Gabriel Minarik, Nikolay A. Barashkov, Elza Khusnutdinova, Ludevit Kadasi, Aisen V. Solovyev, Alexander Poliakov, Mait Metspalu, Alena Kushniarevich, M. R. Lalayants, Fedor M. Teryutin, E. A. Bliznetz, Marita S. Bady-Khoo, T. G. Markova, Ene Metspalu, Sardana A. Fedorova
Publikováno v:
Human Genetics. 141:697-707
Mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have a high ethno-geographic specificity in their distribution, being attributed to a foun
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. 23(23)
Pathogenic variants in the