CYTE-I-HD: Phase I dose finding and tolerability study of cysteamine (Cystagon) in Huntington's disease
Author:
Funder
Research Institute of the University of Kansas Medical Center
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference22 articles.
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2. Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract;Goldberg;Nat Genet,1996
3. Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation;Davies;Cell,1997
4. Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain;DiFiglia;Science,1997
5. Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism;Green;Cell,1993
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