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http://purl.uniprot.org/citations/10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10557097http://www.w3.org/2000/01/rdf-schema#comment"Complex chromosomal rearrangements (deletions, inversions, translocations) are a hallmark of human tumour cells. Yet, the generation of animal models for gross chromosomal abnormalities still presents a formidable challenge. Here, we describe a versatile procedure for chromosomal engineering that was used to generate an ES cell line with a megabase deletion encompassing the tumour suppressor gene neurofibromatosis-1 (Nf-1) on mouse chromosome 11, which is often deleted in tumours of neural crest origin. Homologous recombination into sites flanking Nf-1 was used to introduce artificial sequences (triple-helix, loxP, vector backbone) that can be employed for in vitro recovery of intervening sequences or the generation of in vivo deletions. This strategy may be developed into a scheme by which large chromosomal regions with precisely defined end points may be excised from mammalian cells and reintroduced after suitable in vitro modification."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.org/dc/terms/identifier"doi:10.1038/sj.onc.1203021"xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/author"Schupp I."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/author"Boehm T."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/author"Lichter P."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/author"Kutsche K."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/author"Mincheva A."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/author"Schlake T."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/name"Oncogene"xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/pages"6078-6082"xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/title"Predetermined chromosomal deletion encompassing the Nf-1 gene."xsd:string
http://purl.uniprot.org/citations/10557097http://purl.uniprot.org/core/volume"18"xsd:string
http://purl.uniprot.org/citations/10557097http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10557097
http://purl.uniprot.org/citations/10557097http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10557097
http://purl.uniprot.org/uniprot/#_A0A1W2P863-mappedCitation-10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/#_Q3TYD2-mappedCitation-10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/#_Q04690-mappedCitation-10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/#_Q8BQG3-mappedCitation-10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/#_Q5SYH9-mappedCitation-10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/#_Q8CCE8-mappedCitation-10557097http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/A0A1W2P863http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/Q8CCE8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/10557097
http://purl.uniprot.org/uniprot/Q5SYH9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/10557097