Therapeutic gene silencing strategies for polyglutamine disorders
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference98 articles.
1. Trinucleotide repeat disorders;Orr;Annu. Rev. Neurosci.,2007
2. Huntingtin-protein interactions and the pathogenesis of Huntington's disease;Li;Trends Genet.,2004
3. Properties of human Cav2.1 channel with a spinocerebellar ataxia type 6 mutation expressed in Purkinje cells;Saegusa;Mol. Cell. Neurosci.,2007
4. Polyglutamine-expanded ataxin 7 antagonises CRX function and induces cone-rod dystrophy in a mouse model of SCA7;La Spada;Neuron.,2001
5. SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin 7 in neurons and abnormalities in short-term plasticity;Yoo;Neuron,2003
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