The Familial Amyotrophic Lateral Sclerosis-Associated Amino Acid Substitutions E100G, G93A, and G93R Do Not Influence the Rate of Inactivation of Copper- and Zinc-Containing Superoxide Dismutase by H2O2

This publication has 21 references indexed in Scilit:

• 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
• A Familial Amyotrophic Lateral Sclerosis-associated A4V Cu,Zn-Superoxide Dismutase Mutant Has a Lower K for Hydrogen Peroxide
  Published by Elsevier ,1997
• Genetics of amyotrophic lateral sclerosis
  Human Molecular Genetics, 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
• Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.
  Proceedings of the National Academy of Sciences, 1996
• Altered Reactivity of Superoxide Dismutase in Familial Amyotrophic Lateral Sclerosis
  Science, 1996
• Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS)
  Brain Research, 1995
• Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis.
  Proceedings of the National Academy of Sciences, 1995
• Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide Dismutase
  Science, 1993
• Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
  Nature, 1993