Mitochondrial function in Huntington's disease: Clues for pathogenesis and prospects for treatment
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference11 articles.
1. Energy metabolism defects in Huntington's disease and effects of coenzyme Q10
2. Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
3. Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue
4. Absence of Disease Phenotype and Intergenerational Stability of the Cag Repeat in Transgenic Mice Expressing the Human Huntington Disease Transcript
5. Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract
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4. Cytochromecoxidase isoform IV-2 is involved in 3-nitropropionic acid-induced toxicity in striatal astrocytes;Glia;2009-11-01
5. Striatal gray matter loss in Huntington's disease is leftward biased;Movement Disorders;2007
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