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1 Rouault TA, "The role of iron regulatory proteins in mammalian iron homeostasis and disease" 2 : 406-414, 2006
2 Flint DH, "The inactivation of Fe-S cluster contain- ing hydro-lyases by superoxide" 268 : 22369-22376, 1993
3 Fornstedt B, "The apparent autoxidation rate of catechols in dopaminerich regions of human brains increases with the degree of dep- igmentation of substantia nigra" 1 : 279-295, 1989
4 Fisher DB, "Tetrahydropterin oxidation without hydroxylation catalyzed by rat liver phenylalanine hydroxylase" 248 : 4300-4304, 1973
5 Choi HJ, "Tetrahydrobiopterin is released from and causes preferential death of catecholaminergic cells by oxidative stress" 58 : 633-640, 2000
6 Hausladen A, "Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not" 269 : 29405-29408, 1994
7 Hastings TG, "Role of oxidation in the neurotoxic effects of intrastriatal dopamine injections" 93 : 1956-1961, 1996
8 Longo VD, "Reversible inactivation of superoxide-sensitive aconitase in Abeta1-42-treated neuronal cell lines" 75 : 1977-1985, 2000
9 Han JM, "Protective effect of sulforaphane against dopaminergic cell death" 321 : 249-256, 2007
10 Dunnett SB, "Prospects for new restorative and neuroprotective treatments in parkinson’s disease" 399 : A32-A39, 1999
11 Davis MD, "Products of the tyrosinedependent oxidation of tetrahydrobiopterin by rat liver phenylalanine hydroxylase" 304 : 9-16, 1993
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25 Berman SB, "Dopamine oxidation alters mitochondrial respiration and induces permeability transition in brain mitochondria: implications for Parkinson’s disease" 73 : 1127-1137, 1999
26 Li QY, "Dependence of excitotoxic neurodegeneration on mitochondrial aconitase inactivation" 78 : 746-755, 2001
27 Spencer JP, "Conjugates of catecholamines with cysteine and GSH in Parkinson's disease: possible mechanisms of formation involving reactive oxygen species" 71 : 2112-2122, 1998