Art

J-GLOBAL ID：201602211502297269   Reference number：16A0046289

The role of SIGMAR1 gene mutation and mitochondrial dysfunction in amyotrophic lateral sclerosis

筋萎縮性側索硬化症におけるSIGMAR1遺伝子変異およびミトコンドリア機能障害の役割

Author (3)： FUKUNAGA Kohji (Tohoku Univ., Sendai, JPN) ,  SHINODA Yasuharu (Tohoku Univ., Sendai, JPN) ,  TAGASHIRA Hideaki (Tohoku Univ., Sendai, JPN)
Material： Journal of Pharmacological Sciences (Web)  (J Pharmacol Sci (Web))
Volume： 127  Issue： 1  Page： 36-41 (WEB ONLY)  Publication year： Jan. 2015 
JST Material Number： U0667A  ISSN： 1347-8613  Document type： Article
Article type： 文献レビュー  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： *amyotrophic lateral sclerosis ,...
Semi thesaurus term： *SIGMAR1遺伝子 ,...

Register(free) or Log In to access     To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=16A0046289&from=J-GLOBAL&jstjournalNo=U0667A") }}

JST classification (2)： Nervous system diseases  (GN03000O) ,  Molecular genetics in general  (EC02010J)

Reference (67)：

• Traxinger K, Kelly C, Johnson BA, Lyles RH, Glass JD. Prognosis and epidemiology of amyotrophic lateral sclerosis: analysis of a clinic population, 1997-2011. Neurol Clin Pract. 2013;3:313-320.
• Byrne S, Walsh C, Lynch C, et al. Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis. J Neurol Neurosurg Psychiatry. 2010;82:623-627.
• Pasinelli P, Brown RH. Molecular biology of amyotrophic lateral sclerosis: insights from genetics. Nat Rev Neurosci. 2006;7:710-723.
• Renton AE, Chio A, Traynor BJ. State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci. 2014;17:17-23.
• Rosen DR, Siddique T, Patterson D, et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993;362:59-62.

Terms in the title (4)： 筋萎縮性側索硬化症 ,  遺伝子変異 ,  ミトコンドリア機能障害 ,  役割