共 401 条
[1]
Andrus P.K.(1998)Protein oxidative damage in a transgenic mouse model of familial amyotrophic lateral sclerosis J. Neurochem. 71 2041-2048
[2]
Fleck T.J.(1997)Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis Ann. Neurol. 42 644-654
[3]
Gurney M.E.(1993)Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis J. Neurochem. 61 2322-2325
[4]
Hall E.D.(1994)Nitric oxide: a physiologic messenger molecule Annu. Rev. Biochem. 63 175-195
[5]
Beal M.E(1995)Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates Proc. Natl. Acad. Sci. USA 92 7105-7109
[6]
Ferrante R.J.(1997)Oxidative damage and metabolic dysfunction in Huntington’s disease: selective vulnerability of the basal ganglia Ann. Neurol. 41 646-653
[7]
Browne S.E.(1997)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 Proc. Natl. Acad. Sci. USA 94 7606-7611
[8]
Matthews R.T.(1995) property of one familial ALS-linked Superoxide dismutase 1 mutant Neuroreport 6 711-715
[9]
Kowall N.W.(1997)Distribution of brain cytochrome oxidase activity in various neurodegenerative diseases J. Neurosci. 17 9060-9067
[10]
Brown R.H.(1999)Pyruvate protects neurons against hydrogen peroxide-induced toxicity Science 281 2498-2500