Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sardana K Kononova"'
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:
Sardana K. Kononova, Nikolay A. Barashkov, Ariadna Semenova, Anna N. Romanova, Davydova Tatiana, Valentin Struchkov, Tatiana E. Burtseva, Sargylana Sofronova, Sidorova Oksana, Sardana A. Fedorova, Dekabrina Vinokurova
Publikováno v:
International Journal of Circumpolar Health
article-version (VoR) Version of Record
International Journal of Circumpolar Health, Vol 80, Iss 1 (2021)
article-version (VoR) Version of Record
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
Autor:
Oksana G. Sidorova, Dmitriy G. Tikhonov, Fedor Platonov, Tatyana S. Neustroyeva, Kathrin Tyryshkin, Neil Renwick, Sardana K. Kononova, Natalya V. Yakovleva, Valerian P. Nikolaev, Lev G. Goldfarb, Tatyana M. Sivtseva
Publikováno v:
neurogenetics. 17:179-185
Spinocerebellar ataxia type 1 (SCA1) is the major and likely the only type of autosomal dominant cerebellar ataxia in the Sakha (Yakut) people of Eastern Siberia. The prevalence rate of SCA1 has doubled over the past 21 years peaking at 46 cases per
Autor:
Sardana K. Kononova, Sardana A. Fedorova, Elza Khusnutdinova, Oksana G. Sidorova, V. L. Izhevskaya, Fedor Platonov
Publikováno v:
International Journal of Circumpolar Health, Vol 73, Iss 0, Pp 1-5 (2014)
International Journal of Circumpolar Health
International Journal of Circumpolar Health; Vol 73 (2014)
International Journal of Circumpolar Health
International Journal of Circumpolar Health; Vol 73 (2014)
Background . Prenatal diagnosis of congenital and hereditary diseases is a priority for the development of medical technologies in Russia. However, there are not many published research results on bioethical issues of prenatal DNA testing. Objective
Autor:
Elvira E. Fedotova, Oksana G. Sidorova, Aisen V. Solovyev, Sardana A. Fedorova, Lena M. Vasilyevа, Natalya A. Solovyevа, Anatoliy N. Alekseev, Olga L. Posukh, Nyurgun N. Gotovtsev, Andrey A. Kozhevnikov, Sardana K. Kononova, Georgii P. Romanov, Fedor M. Teryutin, Igor Morozov, Alexander A. Bondar, N. N. Sazonov, Mikhail I. Tomsky, Elena V. Kirillina, Elza Khusnutdinova, A.M. Rafailov, Lilya U. Dzhemileva, Nikolay A. Barashkov, V.G. Pshennikova, Leonid A. Klarov
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 5, p e0156300 (2016)
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
Publikováno v:
Genomics and Health in the Developing World
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4683a79c613037055004d5fb5d02286c
https://doi.org/10.1093/med/9780195374759.003.0120
https://doi.org/10.1093/med/9780195374759.003.0120