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Brain : a Journal of Neurology|October 10, 2003
Minute quantities of misfolded mutant superoxide dismutase-1 cause amyotrophic lateral sclerosisP Andreas Jonsson, Karin Ernhill, Peter M Andersen, et al.
Molecular & Cellular Proteomics : MCP|April 10, 2009
Changes in the spinal cord proteome of an amyotrophic lateral sclerosis murine model determined by differential in-gel electrophoresisDaniel Bergemalm, Karin Forsberg, P Andreas Jonsson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS modelsPer Zetterström, Heather G Stewart, Daniel Bergemalm, et al.
Plos One|July 21, 2010
Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patientsKarin Forsberg, P Andreas Jonsson, Peter M Andersen, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 25, 2015
Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mappingJohan Bergh, Per Zetterström, Peter M Andersen, et al.
Neurobiology of Disease|September 25, 2002
CuZn-superoxide dismutase in D90A heterozygotes from recessive and dominant ALS pedigreesP Andreas Jonsson, Asa Bäckstrand, Peter M Andersen, et al.
Neuron|July 6, 2004
Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondriaJian Liu, Concepción Lillo, P Andreas Jonsson, et al.
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