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Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models.
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2007 (English)In: Proc Natl Acad Sci U S A, ISSN 0027-8424, Vol. 104, no 35, 14157-62 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2007. Vol. 104, no 35, 14157-62 p.
Keyword [en]
Animals, Disease Models; Animal, Humans, Mice, Mice; Transgenic, Motor Neuron Disease/enzymology/*genetics, Mutation, Oxidation-Reduction, Protein Denaturation, Protein Folding, Protein Subunits, Sequence Deletion, Spinal Cord/growth & development/*physiopathology, Superoxide Dismutase/*genetics/metabolism, Variation (Genetics)
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URN: urn:nbn:se:su:diva-22464ISI: 000249187500054PubMedID: 17715066OAI: oai:DiVA.org:su-22464DiVA: diva2:188991
Available from: 2007-12-20 Created: 2007-12-20 Last updated: 2011-01-11Bibliographically approved

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Department of Biochemistry and Biophysics

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