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The Kruppel-like transcription factor KLF13 is a novel regulator of heart development

In humans, congenital heart defects occur in 1–2% of live birth, but the molecular mechanisms and causative genes remain unidentified in the majority of cases. We have uncovered a novel transcription pathway important for heart morphogenesis. We report that KLF13, a member of the Krüppel-like family...

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Bibliographic Details
Main Authors: Lavallée, Geneviève, Andelfinger, Gregor, Nadeau, Mathieu, Lefebvre, Chantal, Nemer, Georges, Horb, Marko E, Nemer, Mona
Format: Artigo
Language:Inglês
Published: 2006
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1630408/
https://ncbi.nlm.nih.gov/pubmed/17053787
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.emboj.7601379
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