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http://purl.uniprot.org/citations/8220435http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8220435http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8220435http://www.w3.org/2000/01/rdf-schema#comment"Familial Alzheimer's disease (FAD) is a genetically heterogeneous disorder that includes a rare early-onset form linked to mutations in the amyloid b protein precursor (APP) gene. Clues to the function of APP derive from the recent finding that it is a member of a highly conserved protein family that includes the mammalian amyloid precursor-like protein (APLP1) gene which maps to the same general region of human chromosome 19 linked to late-onset FAD. Here we report the isolation of the human APLP2 gene. We show that APLP2 is a close relative of APP and exhibits a very similar pattern of expression in the brain and throughout the body. Like APP, APLP2 contains a cytoplasmic domain predicted to couple with the GTP-binding protein G(o) indicating that it may be an additional cell surface activator of this G protein."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.org/dc/terms/identifier"doi:10.1038/ng0993-95"xsd:string
http://purl.uniprot.org/citations/8220435http://purl.org/dc/terms/identifier"doi:10.1038/ng0993-95"xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Neve R.L."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Neve R.L."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Hyman B.T."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Hyman B.T."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Sisodia S.S."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Sisodia S.S."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Tanzi R.E."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Tanzi R.E."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Wasco W."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Wasco W."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Romano D.M."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Romano D.M."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Gurubhagavatula S."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Gurubhagavatula S."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Paradis M."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/author"Paradis M."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/name"Nat. Genet."xsd:string
http://purl.uniprot.org/citations/8220435http://purl.uniprot.org/core/name"Nat. Genet."xsd:string