Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models-Reference-Cited by-同舟云学术

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Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models

Published:2007-08-21 Issue:35 Volume:104 Page:14157-14162
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Zetterstrom P.,Stewart H. G.,Bergemalm D.,Jonsson P. A.,Graffmo K. S.,Andersen P. M.,Brannstrom T.,Oliveberg M.,Marklund S. L.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference30 articles.

1. Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction

2. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

3. Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation

4. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

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