Miro1 deficiency in amyotrophic lateral sclerosis

Proper transportation of mitochondria to sites with high energy demands is critical for neuronal function and survival. Impaired mitochondrial movement has been repeatedly reported in motor neurons of amyotrophic lateral sclerosis (ALS) patients and indicated as an important mechanism contributing t...

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Detalles Bibliográficos
Autores principales: Zhang, Fan, Wang, Wenzhang, Siedlak, Sandra L., Liu, Yingchao, Liu, Jun, Jiang, Keji, Perry, George, Zhu, Xiongwei, Wang, Xinglong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443026/
https://www.ncbi.nlm.nih.gov/pubmed/26074815
http://dx.doi.org/10.3389/fnagi.2015.00100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443026/
https://www.ncbi.nlm.nih.gov/pubmed/26074815
http://dx.doi.org/10.3389/fnagi.2015.00100

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