期刊
ANTIOXIDANTS & REDOX SIGNALING
卷 11, 期 7, 页码 1615-U8出版社
MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2009.2604
关键词
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资金
- NIH/NINDS [R01-NS051419]
- Muscular Dystrophy Association
Perturbation of organellar axonal transport is increasingly recognized as an important contributor in a number of neurodegenerative diseases. Although the specificity of this impairment remains to be elucidated, growing evidence suggests that in certain disease conditions, mitochondria are affected primarily by transport defects. Many hypotheses have been formulated to explain the pathogenic mechanisms involved in amyotrophic lateral sclerosis (ALS). The mutations described so far in genetic forms of ALS (familial ALS, fALS) affect proteins involved in a wide variety of cellular mechanisms, including free radical scavenging, energy metabolism, axonal transport, RNA processing, DNA repair, vesicular transport, and angiogenesis. Here we review the current knowledge on mitochondrial transport and its role in ALS. Antioxid. Redox Signal. 11, 1615-1626.
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