Wild-type PABPN1 is anti-apoptotic and reduces toxicity of the oculopharyngeal muscular dystrophy mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/17/8/1097/17245769/ddm382.pdf
Reference42 articles.
1. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat. Genet,1998
2. Oculopharyngeal muscular dystrophy: recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies;Abu-Baker;Biochim. Biophys. Acta,2007
3. Oculopharyngeal muscular dystrophy: potential therapies for an aggregate-associated disorder;Davies;Int. J. Biochem. Cell Biol,2006
4. Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA;Calado;Hum. Mol. Genet,2000
5. Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy;Tome;Neuromuscul. Disord,1997
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