Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Vera G Pshennikova"'
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
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:
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
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; Volume 13; Issue 9; Pages: 1612
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
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; Volume 11; Issue 2; Pages: 257
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
Autor:
Aisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, Marita Bady-Khoo, Maria R Lalayants, Tatiana G Markova, Gabriel Minárik, L'udevít Kádasi, Ene Metspalu, Vera G Pshennikova, Fedor M Teryutin, Anatoly N Alekseev, Elza K Khusnutdinova, Alexander Poliakov, Mait Мetspalu, Olga L Posukh, Nikolay A Barashkov, Sardana A Fedorova
The 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 high ethno-geographic specificity in their distribution that being attributed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a1dcbfd6f9ec92417babfcf62bd10b3
https://doi.org/10.21203/rs.3.rs-670020/v1
https://doi.org/10.21203/rs.3.rs-670020/v1
Autor:
Aisen V, Solovyev, Alena, Kushniarevich, Elena, Bliznetz, Marita, Bady-Khoo, Maria R, Lalayants, Tatiana G, Markova, Gabriel, Minárik, L'udevít, Kádasi, Ene, Metspalu, Vera G, Pshennikova, Fedor M, Teryutin, Elza K, Khusnutdinova, Alexander, Poliakov, Mait, Metspalu, Olga L, Posukh, Nikolay A, Barashkov, Sardana A, Fedorova
Publikováno v:
Human genetics. 141(3-4)
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