Minute quantities of misfolded mutant superoxide dismutase‐1 cause amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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Minute quantities of misfolded mutant superoxide dismutase‐1 cause amyotrophic lateral sclerosis

Published:2004-01 Issue:1 Volume:127 Page:73-88
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Jonsson P. Andreas,Ernhill Karin,Andersen Peter M.,Bergemalm Daniel,Brännström Thomas,Gredal Ole,Nilsson Peter,Marklund Stefan L.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/127/1/73/17868872/awh005.pdf

Reference50 articles.

1. Andersen PM, Nilsson P, Ala‐Hurula V, Keranen ML, Tarvainen I, Haltia T, et al. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn‐superoxide dismutase. Nat Genet1995; 10: 61–6.

2. Andersen PM, Nilsson P, Keranen ML, Forsgren L, Hagglund J, Karlsborg M, et al. Phenotypic heterogeneity in motor neuron disease patients with CuZn‐superoxide dismutase mutations in Scandinavia. Brain1997; 120: 1723–37.

3. Andersen PM, Sims KB, Xin WW, Kiely R, O’Neill G, Ravits J, et al. Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes. Amyotroph Lateral Scler Other Motor Neuron Disord2003; 2: 62–73.

4. Beauchamp C, Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem1971; 44: 276–87.

5. Bendotti C, Calvaresi N, Chiveri L, Prelle A, Moggio M, Braga M, et al. Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity. J Neurol Sci2001; 191: 25–33.

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