Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Svetlana Alksandrovna El′chaninova"'
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