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http://purl.uniprot.org/citations/9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/9371501http://www.w3.org/2000/01/rdf-schema#comment"Apc-associated intestinal tumor formation appears to require functional loss of both Apc alleles. Apc has, therefore, been classified as a tumor suppressor gene. Loss of APC protein function results in increased intracellular beta-catenin, a molecule important to both cell-cell adhesion and regulation of cellular growth. In mice bearing a germ-line Apc mutation, we found that enterocyte beta-catenin expression was also increased in histologically normal intestinal mucosa. Enterocyte crypt-villus migration was decreased by 25%, and treatment of Min/+ animals with sulindac sulfide normalized both beta-catenin expression and enterocyte migration. Our data suggest that alterations in enterocyte migration occur in cells bearing a single mutant Apc allele, and that sulindac sulfide may normalize enterocyte growth in these cells."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/author"Martucci C."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/author"Mahmoud N.N."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/author"Bertagnolli M.M."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/author"Boolbol S.K."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/author"Chadburn A."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/author"Bilinski R.T."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/date"1997"xsd:gYear
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/name"Cancer Res"xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/pages"5045-5050"xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/title"Apc gene mutation is associated with a dominant-negative effect upon intestinal cell migration."xsd:string
http://purl.uniprot.org/citations/9371501http://purl.uniprot.org/core/volume"57"xsd:string
http://purl.uniprot.org/citations/9371501http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/9371501
http://purl.uniprot.org/citations/9371501http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/9371501
http://purl.uniprot.org/uniprot/Q61315#attribution-052632992C1E2195F0206EBEC6550E98http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_B2RUG9-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_E9QLQ9-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_F6Z405-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_P70382-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_E9Q4H1-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_F6Q4R2-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_Q8BRD8-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_Q3UQT2-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501
http://purl.uniprot.org/uniprot/#_Q8BNP7-mappedCitation-9371501http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9371501