Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
25
pubmed:dateCreated
2002-12-11
pubmed:abstractText
Ventricular septal defects are common in human infants, but the genetic programs that control ventricular septation are poorly understood. Here we report that mice with a targeted disruption of the cardiovascular basic helix-loop-helix factor (CHF)1Hey2 gene show isolated ventricular septal defects. These defects result primarily in failure to thrive. Mice often succumbed within the first 3 wk after birth and showed pulmonary and liver congestion. The penetrance of this phenotype varied, depending on genetic background, suggesting the presence of modifier genes. Expression patterns of other cardiac-specific genes were not affected. Of the few animals on a mixed genetic background that survived to adulthood, most developed a cardiomyopathy but did not have ventricular septal defects. Our results indicate that CHF1 plays an important role in regulation of ventricular septation in mammalian heart development and is important for normal myocardial contractility. These mice provide a useful model for the study of the ontogeny and natural history of ventricular septal defects and cardiomyopathy.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10373308, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10403790, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10415358, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10545522, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10587520, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10692439, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10710309, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10807864, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10860664, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10888889, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-10892744, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11069914, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11076679, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11095750, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11158594, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11160397, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11238910, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11279181, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11424141, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11437450, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11486044, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11486045, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11514558, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11572777, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11700560, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11788824, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11788825, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-11840327, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-12372253, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-12372254, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-6744353, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-7615798, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-7690144, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-8114858, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-8227090, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-8533092, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-8823298, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9039266, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9281443, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9515963, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9515964, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9546373, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9616213, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9651244, http://linkedlifedata.com/resource/pubmed/commentcorrection/12454287-9884344
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
99
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
16197-202
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:12454287-Animals, pubmed-meshheading:12454287-Basic Helix-Loop-Helix Transcription Factors, pubmed-meshheading:12454287-Calcinosis, pubmed-meshheading:12454287-Cardiomyopathies, pubmed-meshheading:12454287-Cardiomyopathy, Dilated, pubmed-meshheading:12454287-Failure to Thrive, pubmed-meshheading:12454287-Female, pubmed-meshheading:12454287-Gene Targeting, pubmed-meshheading:12454287-Genetic Predisposition to Disease, pubmed-meshheading:12454287-Genotype, pubmed-meshheading:12454287-Heart Septal Defects, Ventricular, pubmed-meshheading:12454287-Heart Septum, pubmed-meshheading:12454287-Male, pubmed-meshheading:12454287-Mice, pubmed-meshheading:12454287-Mice, Inbred C57BL, pubmed-meshheading:12454287-Mice, Knockout, pubmed-meshheading:12454287-Morphogenesis, pubmed-meshheading:12454287-Myocardial Contraction, pubmed-meshheading:12454287-Repressor Proteins
pubmed:year
2002
pubmed:articleTitle
Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2.
pubmed:affiliation
Vascular Medicine Research, Brigham and Women's Hospital and Harvard Medical School, Cambridge, MA 02139, USA.
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