Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fedor A. Platonov"'
Autor:
Sardana K. Kononova, Oksana G. Sidorova, Sardana A. Fedorova, Fedor A. Platonov, Vera L. Izhevskaya, Elza K. Khusnutdinova
Publikováno v:
International Journal of Circumpolar Health, Vol 73, Iss 0, Pp 1-5 (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:
Externí odkaz:
https://doaj.org/article/96413f07fbe647d48b514cfbb714fb80
Autor:
Ekaterina Alekseevna Sokolova, Nadezhda Alekseevna Malkova, Denis Sergeevich Korobko, Aleksey Sergeevich Rozhdestvenskii, Anastasia Vladimirovna Kakulya, Elena Vladimirovna Khanokh, Roman Andreevich Delov, Fedor Alekseevich Platonov, Tatyana Yegorovna Popova, Elena Gennadievna Aref' eva, Natalia Nikolaevna Zagorskaya, Valentina Mikhailovna Alifirova, Marina Andreevna Titova, Inna Vadimovna Smagina, Svetlana Alksandrovna El' chaninova, Anna Valentinovna Popovtseva, Valery Pavlovich Puzyrev, Olga Georgievna Kulakova, Ekaterina Yur'evna Tsareva, Olga Olegovna Favorova, Sergei Gennadievich Shchur, Natalia Yurievna Lashch, Natalia Fyodorovna Popova, Ekaterina Valerievna Popova, Evgenii Ivanovich Gusev, Aleksey Nikolaevich Boyko, Yurii Sergeevich Aulchenko, Maxim Leonidovich Filipenko
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61032 (2013)
Multiple sclerosis (MS) is a serious, incurable neurological disease. In 2009, the ANZgene studies detected the suggestive association of located upstream of CD40 gene in chromosome 20q13 (p = 1.3×10(-7)). Identification of the causal variant(s) in
Externí odkaz:
https://doaj.org/article/5420b759ae6745f08f4391af5e65c07c
Autor:
Fedor Alekseevich Platonov, Natalia Yurievna Lashch, Yurii S. Aulchenko, Olga Kulakova, Maxim L. Filipenko, Aleksey Sergeevich Rozhdestvenskii, Natalia Fyodorovna Popova, V. P. Puzyrev, N A Malkova, O O Favorova, D. S. Korobko, Tatyana Yegorovna Popova, Sergei Gennadievich Shchur, I. V. Smagina, Svetlana Alksandrovna El′chaninova, Ekaterina Popova, M. Titova, Anna Valentinovna Popovtseva, Aleksey Nikolaevich Boyko, E. I. Gusev, Elena Gennadievna Aref′eva, Anastasia Vladimirovna Kakulya, Natalia Nikolaevna Zagorskaya, Delov Ra, Valentina M. Alifirova, Ekaterina A. Sokolova, Khanokh Ev, Ekaterina Yur'evna Tsareva
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61032 (2013)
PLoS ONE
PLoS ONE
Multiple sclerosis (MS) is a serious, incurable neurological disease. In 2009, the ANZgene studies detected the suggestive association of located upstream of CD40 gene in chromosome 20q13 (p = 1.3×10(-7)). Identification of the causal variant(s) in
Autor:
Anastasia Vladimirovna Kakulya, Maxim L. Filipenko, Anna G. Zolovkina, M. Titova, Valerii P. Puzyrev, Natalia Nikolaevna Zagorskaya, Aleksei S. Rozhdestvenskii, Elena Gennadievna Aref′eva, D. S. Korobko, Delov Ra, N A Malkova, Sergei A. Babenko, I. V. Smagina, Valentina M. Aliferova, Khanokh Ev, G. I. Lifshits, Ekaterina A. Kudryavtseva, Svetlana Alksandrovna El′chaninova, Fedor Alekseevich Platonov
Publikováno v:
Molecular genetics and metabolism. 104(3)
Axonal degeneration is responsible for the progression of the irreversible destruction caused by multiple sclerosis (MS) resulting ultimately in permanent disability. The KIF1B protein, a member of the kinesin family, is necessary for axon growth and
Autor:
Sokolova, Ekaterina Alekseevna1 sokolovaea2608@gmail.ru, Malkova, Nadezhda Alekseevna2, Korobko, Denis Sergeevich2, Rozhdestvenskii, Aleksey Sergeevich3, Kakulya, Anastasia Vladimirovna4, Khanokh, Elena Vladimirovna5, Delov, Roman Andreevich3, Platonov, Fedor Alekseevich6, Popova, Tatyana Yegorovna7, Aref′eva, Elena Gennadievna8, Zagorskaya, Natalia Nikolaevna8, Alifirova, Valentina Mikhailovna9, Titova, Marina Andreevna9, Smagina, Inna Vadimovna10,11, El′chaninova, Svetlana Alksandrovna11, Popovtseva, Anna Valentinovna11, Puzyrev, Valery Pavlovich12, Kulakova, Olga Georgievna13, Tsareva, Ekaterina Yur'evna13, Favorova, Olga Olegovna13
Publikováno v:
PLoS ONE. Apr2013, Vol. 8 Issue 4, p1-8. 8p.
Bioethical issues of preventing hereditary diseases with late onset in the Sakha Republic (Yakutia).
Autor:
Kononova, Sardana K., Sidorova, Oksana G., Fedorova, Sardana A., Platonov, Fedor A., Izhevskaya, Vera L., Khusnutdinova, Elza K.
Publikováno v:
International Journal of Circumpolar Health; Jan2014, Vol. 73, p1-N.PAG, 5p