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http://purl.uniprot.org/citations/10699173http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10699173http://www.w3.org/2000/01/rdf-schema#comment"Huntington's disease (HD) is caused by an expanded N-terminal glutamine tract that endows huntingtin with a striatal-selective structural property ultimately toxic to medium spiny neurons. In precise genetic models of juvenile HD, HdhQ92 and HdhQ111 knock-in mice, long polyglutamine segments change huntingtin's physical properties, producing HD-like in vivo correlates in the striatum, including nuclear localization of a version of the full-length protein predominant in medium spiny neurons, and subsequent formation of N-terminal inclusions and insoluble aggregate. These changes show glutamine length dependence and dominant inheritance with recruitment of wild-type protein, critical features of the altered HD property that strongly implicate them in the HD disease process and that suggest alternative pathogenic scenarios: the effect of the glutamine tract may act by altering interaction with a critical cellular constituent or by depleting a form of huntingtin essential to medium spiny striatal neurons."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.org/dc/terms/identifier"doi:10.1093/hmg/9.4.503"xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Yi H."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"White J.K."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Gusella J.F."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Li X.J."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Li S.H."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"MacDonald M.E."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Joyner A.L."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Weaver M."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Vrbanac V."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Gutekunst C.A."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Auerbach W."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Vonsattel J.P."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Wheeler V.C."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/author"Hersch S."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/date"2000"xsd:gYear
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/name"Hum Mol Genet"xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/pages"503-513"xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/title"Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice."xsd:string
http://purl.uniprot.org/citations/10699173http://purl.uniprot.org/core/volume"9"xsd:string
http://purl.uniprot.org/citations/10699173http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10699173
http://purl.uniprot.org/citations/10699173http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10699173
http://purl.uniprot.org/uniprot/P42859#attribution-BFB834433B62C1867632888268EC5DEDhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10699173