Canine degenerative myelopathy: Biochemical characterization of superoxide dismutase 1 in the first naturally occurring non-human amyotrophic lateral sclerosis model-Reference-Cited by-同舟云学术

Canine degenerative myelopathy: Biochemical characterization of superoxide dismutase 1 in the first naturally occurring non-human amyotrophic lateral sclerosis model

Published:2013-10 Issue: Volume:248 Page:1-9
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Crisp Matthew J.,Beckett Jeffrey,Coates Joan R.,Miller Timothy M.

Funder

NIH/NINDS/AFAR

NINDS

NIH/NINDS

AKC Canine Health Foundation

ALS Association

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

Reference35 articles.

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3. Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1;Bruijn;Science,1998

4. Neuroblastoma×spinal cord (NSC) hybrid cell lines resemble developing motor neurons;Cashman;Dev. Dyn.,1992

5. Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis;Chia;PLoS One,2010

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