Title : Oxidative stress and mitochondrial dysfunction in neurodegeneration.

Pub. Date : 1996 Aug

PMID : 8858182






1 Functional Relationships(s)
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1 The confirmation of the complex II inhibitor 3-nitropropionic acid as a toxin model for Huntington"s disease, together with the demonstration of reduced mitochondrial function in Huntington"s disease caudate, supports the proposition that mutant huntingtin may exert its effect through an abnormality of energy metabolism. 3-nitropropionic acid huntingtin Homo sapiens