In vivo peroxidative activity of FALS-mutant human CuZnSODs expressed in yeast

This publication has 30 references indexed in Scilit:

• Reactions of Hydrogen Peroxide with Familial Amyotrophic Lateral Sclerosis Mutant Human Copper-Zinc Superoxide Dismutases Studied by Pulse Radiolysis
  Journal of Biological Chemistry, 1998
• Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superoxide dismutase 1 mutant
  Proceedings of the National Academy of Sciences, 1997
• A low expressor line of transgenic mice carrying a mutant human Cu,Zn superoxide dismutase ( SOD1 ) gene develops pathological changes that most closely resemble those in human amyotrophic lateral sclerosis
  Acta Neuropathologica, 1997
• Transgenic animal models of familial amyotrophic lateral sclerosis
  Zeitschrift für Neurologie, 1997
• A Familial Amyotrophic Lateral Sclerosis-associated A4V Cu,Zn-Superoxide Dismutase Mutant Has a Lower K for Hydrogen Peroxide
  Published by Elsevier ,1997
• An update on superoxide dismutase 1 in familial amyotrophic lateral sclerosis
  Journal of the Neurological Sciences, 1996
• A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide.
  Proceedings of the National Academy of Sciences, 1996
• Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury
  Nature Genetics, 1996
• Altered Reactivity of Superoxide Dismutase in Familial Amyotrophic Lateral Sclerosis
  Science, 1996
• Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation
  Science, 1994