Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1998-3-11
pubmed:abstractText
Centromere protein C (CENPC) is a key protein that has been localized to the inner kinetochore plate of active mammalian centromeres. Using gene targeting techniques, we have disrupted the mouse Cenpc gene and shown that the gene is essential for normal mouse embryonic development. Heterozygous mice carrying one functional copy of the gene are healthy and fertile, whereas homozygous embryos fail to thrive. In these embryos, mitotic arrest and gross morphological degeneration become apparent as early as the morula stage of development. The degenerating embryos demonstrate highly irregular cell and nuclear morphologies, including the presence of a large number of micronuclei. Mitotic chromosomes of these embryos display a scattered and often highly condensed configuration and do not segregate in an ordered fashion. These results describing the phenotype of the mutant mouse embryos indicate that CENPC has a direct role in the mitotic progression from metaphase to anaphase.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1339310, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1406971, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1541640, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-15957216, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1643659, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1730770, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1819515, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-1997204, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2005906, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2023923, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2138512, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2265565, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2475307, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2579778, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-2808515, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-3211746, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-3464952, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-3909945, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7502067, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7579695, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7579707, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7618084, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7618085, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7684888, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7757082, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7854422, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-7959789, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-8175879, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-8183905, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-8408221, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-8416980, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-8500169, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-8668174, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-9171825, http://linkedlifedata.com/resource/pubmed/commentcorrection/9448298-9259264
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
3
pubmed:volume
95
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1136-41
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
Targeted disruption of mouse centromere protein C gene leads to mitotic disarray and early embryo death.
pubmed:affiliation
The Murdoch Institute for Research into Birth Defects, Royal Children's Hospital, Flemington Road, Melbourne 3052, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't