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Publication : Mitochondria and ALS: implications from novel genes and pathways.

First Author  Cozzolino M Year  2013
Journal  Mol Cell Neurosci Volume  55
Pages  44-9 PubMed ID  22705710
Mgi Jnum  J:203599 Mgi Id  MGI:5527512
Doi  10.1016/j.mcn.2012.06.001 Citation  Cozzolino M, et al. (2013) Mitochondria and ALS: implications from novel genes and pathways. Mol Cell Neurosci 55:44-9
abstractText  Evidence from patients with sporadic and familiar amyotrophic lateral sclerosis (ALS) and from models based on the overexpression of mutant SOD1 found in a small subset of patients, clearly point to mitochondrial damage as a relevant facet of this neurodegenerative condition. In this mini-review we provide a brief update on the subject in the light of newly discovered genes (such as TDP-43 and FUS/TLS) associated to familial ALS and of a deeper knowledge of the mechanisms of derangement of mitochondria. This article is part of a Special Issue entitled 'Mitochondrial function and dysfunction in neurodegeneration'.
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