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http://purl.uniprot.org/citations/11283611http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11283611http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11283611http://www.w3.org/2000/01/rdf-schema#comment"The survival motor neurons (smn) gene in mice is essential for embryonic viability. In humans, mutation of the telomeric copy of the SMN1 gene causes spinal muscular atrophy, an autosomal recessive disease. Here we report that the SMN protein interacts with the zinc-finger protein ZPR1 and that these proteins colocalize in small subnuclear structures, including gems and Cajal bodies. SMN and ZPR1 redistribute from the cytoplasm to the nucleus in response to serum. This process is disrupted in cells from patients with Werdnig-Hoffman syndrome (spinal muscular atrophy type I) that have SMN1 mutations. Similarly, decreased ZPR1 expression prevents SMN localization to nuclear bodies. Our data show that ZPR1 is required for the localization of SMN in nuclear bodies."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.org/dc/terms/identifier"doi:10.1038/35070059"xsd:string
http://purl.uniprot.org/citations/11283611http://purl.org/dc/terms/identifier"doi:10.1038/35070059"xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Sharma M."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Sharma M."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Davis R.J."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Davis R.J."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Gangwani L."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Gangwani L."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Mikrut M."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Mikrut M."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Theroux S."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/author"Theroux S."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/name"Nat. Cell Biol."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/name"Nat. Cell Biol."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/pages"376-383"xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/pages"376-383"xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/title"Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/title"Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein."xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/volume"3"xsd:string
http://purl.uniprot.org/citations/11283611http://purl.uniprot.org/core/volume"3"xsd:string