RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16769089http://www.w3.org/2000/01/rdf-schema#comment"Several mouse models with defects in genes encoding components of the nucleotide excision repair (NER) pathway have been developed. In NER two different sub-pathways are known, i.e. transcription-coupled repair (TC-NER) and global-genome repair (GG-NER). A defect in one particular NER protein can lead to a (partial) defect in GG-NER, TC-NER or both. GG-NER defects in mice predispose to cancer, both spontaneous as well as UV-induced. As such these models (Xpa, Xpc and Xpe) recapitulate the human xeroderma pigmentosum (XP) syndrome. Defects in TC-NER in humans are associated with Cockayne syndrome (CS), a disease not linked to tumor development. Mice with TC-NER defects (Csa and Csb) are - except for the skin - not susceptible to develop (carcinogen-induced) tumors. Some NER factors, i.e. XPB, XPD, XPF, XPG and ERCC1 have functions outside NER, like transcription initiation and inter-strand crosslink repair. Deficiencies in these processes in mice lead to very severe phenotypes, like trichothiodystrophy (TTD) or a combination of XP and CS. In most cases these animals have a (very) short life span, display segmental progeria, but do not develop tumors. Here we will overview the available NER-related mouse models and will discuss their phenotypes in terms of (chemical-induced) tissue-specific tumor development, mutagenesis and premature aging features."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.org/dc/terms/identifier"doi:10.1016/j.mrfmmm.2005.12.018"xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/author"van der Horst G.T."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/author"van Steeg H."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/author"de Waard H."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/author"Wijnhoven S.W."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/author"Hoogervorst E.M."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/name"Mutat Res"xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/pages"77-94"xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/title"Tissue specific mutagenic and carcinogenic responses in NER defective mouse models."xsd:string
http://purl.uniprot.org/citations/16769089http://purl.uniprot.org/core/volume"614"xsd:string
http://purl.uniprot.org/citations/16769089http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16769089
http://purl.uniprot.org/citations/16769089http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16769089
http://purl.uniprot.org/uniprot/#_A0A0U1RP06-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_A0A0U1RNS4-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_A0A2I3BQP1-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_D3YU16-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_D6RIM0-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_F8VPZ5-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_D6RET0-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_D6RHP2-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_F6QML7-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089
http://purl.uniprot.org/uniprot/#_F6QPY9-mappedCitation-16769089http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16769089