Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
22
pubmed:dateCreated
1989-12-21
pubmed:abstractText
We have inactivated, by gene targeting, the endogenous beta 2-microglobulin gene in a mouse embryonic stem cell line. A cloned fragment of the beta 2-microglobulin gene with the coding sequence disrupted by the insertion of the neomycin-resistance gene was used to transfect the embryonic stem cells. G418-resistant colonies were selected and then screened using the polymerase chain reaction to identify those in which the incoming DNA had integrated into the embryonic stem cell genome by homologous recombination. Of a total of 234 G418-resistant colonies screened, 2 correctly targeted colonies were identified. Chimeric mice carrying the inactivated beta 2-microglobulin gene have been obtained from both of these targeted embryonic cell lines. Breeding of offspring from such animals will allow investigation of the effects of homozygous loss of beta 2-microglobulin.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-2443855, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-2563902, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-2573070, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-2581247, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-2822260, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-2912572, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3024164, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3174435, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3194019, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3464450, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3593833, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3683574, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3821905, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-3897439, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-6170985, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-6171732, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-6180834, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-6188162, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-6317199, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-7120180, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-7242681, http://linkedlifedata.com/resource/pubmed/commentcorrection/2682666-92183
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:volume
86
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8932-5
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:2682666-Animals, pubmed-meshheading:2682666-Base Sequence, pubmed-meshheading:2682666-Blastocyst, pubmed-meshheading:2682666-Blotting, Southern, pubmed-meshheading:2682666-Cell Line, pubmed-meshheading:2682666-Cells, Cultured, pubmed-meshheading:2682666-DNA, pubmed-meshheading:2682666-Exons, pubmed-meshheading:2682666-Female, pubmed-meshheading:2682666-Genes, pubmed-meshheading:2682666-Hematopoietic Stem Cells, pubmed-meshheading:2682666-Introns, pubmed-meshheading:2682666-Male, pubmed-meshheading:2682666-Mice, pubmed-meshheading:2682666-Mice, Inbred C57BL, pubmed-meshheading:2682666-Mice, Inbred Strains, pubmed-meshheading:2682666-Oligonucleotide Probes, pubmed-meshheading:2682666-Plasmids, pubmed-meshheading:2682666-Polymerase Chain Reaction, pubmed-meshheading:2682666-Recombination, Genetic, pubmed-meshheading:2682666-beta 2-Microglobulin
pubmed:year
1989
pubmed:articleTitle
Inactivating the beta 2-microglobulin locus in mouse embryonic stem cells by homologous recombination.
pubmed:affiliation
Department of Pathology, University of North Carolina, Chapel Hill 27599-7525.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't