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http://purl.uniprot.org/citations/7806582http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7806582http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7806582http://www.w3.org/2000/01/rdf-schema#comment"beta-Catenin is involved in the formation of adherens junctions of mammalian epithelia. It interacts with the cell adhesion molecule E-cadherin and also with the tumor suppressor gene product APC, and the Drosophila homologue of beta-catenin, armadillo, mediates morphogenetic signals. We demonstrate here that E-cadherin and APC directly compete for binding to the internal, armadillo-like repeats of beta-catenin; the NH2-terminal domain of beta-catenin mediates the interaction of the alternative E-cadherin and APC complexes to the cytoskeleton by binding to alpha-catenin. Plakoglobin (gamma-catenin), which is structurally related to beta-catenin, mediates identical interactions. We thus show that the APC tumor suppressor gene product forms strikingly similar associations as found in cell junctions and suggest that beta-catenin and plakoglobin are central regulators of cell adhesion, cytoskeletal interaction, and tumor suppression."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.org/dc/terms/identifier"doi:10.1083/jcb.127.6.2061"xsd:string
http://purl.uniprot.org/citations/7806582http://purl.org/dc/terms/identifier"doi:10.1083/jcb.127.6.2061"xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/author"Behrens J."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/author"Behrens J."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/author"Birchmeier W."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/author"Birchmeier W."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/author"Huelsken J."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/author"Huelsken J."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/name"J. Cell Biol."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/name"J. Cell Biol."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/pages"2061-2069"xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/pages"2061-2069"xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/title"E-cadherin and APC compete for the interaction with beta-catenin and the cytoskeleton."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/title"E-cadherin and APC compete for the interaction with beta-catenin and the cytoskeleton."xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/volume"127"xsd:string
http://purl.uniprot.org/citations/7806582http://purl.uniprot.org/core/volume"127"xsd:string
http://purl.uniprot.org/citations/7806582http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7806582
http://purl.uniprot.org/citations/7806582http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7806582
http://purl.uniprot.org/citations/7806582http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7806582
http://purl.uniprot.org/citations/7806582http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7806582