17483304

Source:http://linkedlifedata.com/resource/pubmed/id/17483304

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007634, umls-concept:C0022702, umls-concept:C0026882, umls-concept:C0036667, umls-concept:C0086418, umls-concept:C0205225, umls-concept:C0205234, umls-concept:C0205349, umls-concept:C0312418, umls-concept:C0332281, umls-concept:C0879290, umls-concept:C1419240, umls-concept:C1522449
pubmed:issue	8
pubmed:dateCreated	2007-8-3
pubmed:abstractText	Reports of differential mutagen sensitivity conferred by a defect in the mismatch repair (MMR) pathway are inconsistent in their conclusions. Previous studies have investigated cells established from immortalised human colorectal tumour lines or cells from animal models.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-10334196, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-10590226, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-11283247, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-11790664, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-11809679, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-11929830, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-12549480, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-12687013, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-14522371, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-14744114, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-15279797, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-15735976, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-15814658, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-15860725, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-16283678, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-16357213, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-7628020, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-7840761, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-9371516, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-9443401, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-9485033, http://linkedlifedata.com/resource/pubmed/commentcorrection/17483304-9751765
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/MSH2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/MutS Homolog 2 Protein, http://linkedlifedata.com/resource/pubmed/chemical/RAD51 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Rad51 Recombinase
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1468-6244
pubmed:author	pubmed-author:BarwellJJ, pubmed-author:BrinkmanHH, pubmed-author:CamplejohnRR, pubmed-author:DochertyZZ, pubmed-author:GeorgiouAA, pubmed-author:HodgsonSS, pubmed-author:HomfrayTT, pubmed-author:KestertonII, pubmed-author:MorrisJ RJR, pubmed-author:PangonLL, pubmed-author:PayneS JSJ, pubmed-author:SebireN JNJ, pubmed-author:SladeTT, pubmed-author:SmytheJJ, pubmed-author:SolomonEE, pubmed-author:TaylorMM
pubmed:issnType	Electronic
pubmed:volume	44
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	516-20
pubmed:dateRevised	2010-9-14
pubmed:meshHeading	pubmed-meshheading:17483304-Child, Preschool, pubmed-meshheading:17483304-DNA Repair, pubmed-meshheading:17483304-Female, pubmed-meshheading:17483304-Genotype, pubmed-meshheading:17483304-Heterozygote Detection, pubmed-meshheading:17483304-Humans, pubmed-meshheading:17483304-Lymphoma, Non-Hodgkin, pubmed-meshheading:17483304-Male, pubmed-meshheading:17483304-MutS Homolog 2 Protein, pubmed-meshheading:17483304-Mutation, pubmed-meshheading:17483304-Neoplasms, pubmed-meshheading:17483304-Nuclear Family, pubmed-meshheading:17483304-Pedigree, pubmed-meshheading:17483304-Polymorphism, Single Nucleotide, pubmed-meshheading:17483304-Rad51 Recombinase, pubmed-meshheading:17483304-Radiation Tolerance, pubmed-meshheading:17483304-Recombination, Genetic
pubmed:year	2007
pubmed:articleTitle	Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics.
pubmed:affiliation	Department of Genetics, St. George's Medical School, University of London, Cranmer Terrace, London, UK. jo.morris@genetics.kcl.ac.uk
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't