Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca²⁺ concentration in transfected neuroblastoma SH‐SY5Y cells

This publication has 27 references indexed in Scilit:

• Amyotrophic lateral sclerosis is a multifactorial disease
  Muscle & Nerve, 1995
• An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
  Neuron, 1995
• Amyotrophic lateral sclerosis: Recent insights from genetics and transgenic mice
  Cell, 1995
• Bioenergetic and oxidative stress in neurodegenerative diseases
  Life Sciences, 1995
• Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis
  FEBS Letters, 1994
• The role of calcium‐binding proteins in selective motoneuron vulnerability in amyotrophic lateral sclerosis
  Annals of Neurology, 1994
• A New Method for the Cytofluorometric Analysis of Mitochondrial Membrane Potential Using the J-Aggregate Forming Lipophilic Cation 5,5′,6,6′-Tetrachloro-1,1′,3,3′-tetraethylbenzimidazolcarbocyanine Iodide (JC-1)
  Biochemical and Biophysical Research Communications, 1993
• 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
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970