Zobrazeno 1 - 4
of 4
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:
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:
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