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http://purl.uniprot.org/citations/11136710http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11136710http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11136710http://www.w3.org/2000/01/rdf-schema#comment"Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disease caused by the expansion of a polyglutamine tract within the SCA1 product, ataxin-1. Previously, using transgenic mice, it was demonstrated that in order for a mutant allele of ataxin-1 to cause disease it must be transported to the nucleus of the neuron. Using an in vitro RNA-binding assay, we demonstrate that ataxin-1 does bind RNA and that this binding diminishes as the length of its polyglutamine tract increases. These observations suggest that ataxin-1 plays a role in RNA metabolism and that the expansion of the polyglutamine tract may alter this function."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.org/dc/terms/identifier"doi:10.1093/hmg/10.1.25"xsd:string
http://purl.uniprot.org/citations/11136710http://purl.org/dc/terms/identifier"doi:10.1093/hmg/10.1.25"xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Orr H.T."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Orr H.T."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Zoghbi H.Y."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Zoghbi H.Y."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Serra H.G."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Serra H.G."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Yue S."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/author"Yue S."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/name"Hum. Mol. Genet."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/name"Hum. Mol. Genet."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/pages"25-30"xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/pages"25-30"xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/title"The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/title"The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract."xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/11136710http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/11136710http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11136710
http://purl.uniprot.org/citations/11136710http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11136710