RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22905719http://www.w3.org/2000/01/rdf-schema#comment"PER2 is a key mammalian circadian clock protein. It also has a tumor suppressive function. Down regulation of PER2 in the cultured cancer cells accelerates cell proliferation, while overexpression of PER2 inhibits cell growth and induces apoptosis. The Per2 mutant mice have a cancer prone phenotype and an altered DNA damage response. Here we report that PER2 regulates AKT activity. Cells with down-regulated PER2 expression have prolonged high levels of AKT T308 phosphorylation after growth factor stimulation or DNA damage. PER2 down-regulation delays DNA damage induced Chk2 activation and overrides DNA damage induced apoptosis and cell cycle arrest."xsd:string
http://purl.uniprot.org/citations/22905719http://purl.org/dc/terms/identifier"doi:10.1139/o2012-025"xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/author"He X."xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/author"Yang X."xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/author"Yang Z."xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/author"Jabbari E."xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/name"Biochem Cell Biol"xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/pages"675-682"xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/title"Mammalian PER2 regulates AKT activation and DNA damage response."xsd:string
http://purl.uniprot.org/citations/22905719http://purl.uniprot.org/core/volume"90"xsd:string
http://purl.uniprot.org/citations/22905719http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22905719
http://purl.uniprot.org/citations/22905719http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22905719
http://purl.uniprot.org/uniprot/#_A0A0R4J0U3-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_A2VCR5-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_O54943-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_P31749-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_Q3TW41-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_Q3TN36-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_Q7TMG5-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_Q80U32-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/#_Q8C8R0-mappedCitation-22905719http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/Q3TN36http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22905719
http://purl.uniprot.org/uniprot/O54943http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22905719