Induction of apoptosis and inhibition of cell growth by <it>tbx5 </it>knockdown contribute to dysmorphogenesis in Zebrafish embryos
<p>Abstract</p> <p>Background</p> <p>The tbx5 mutation in human causes Holt-Oram syndrome, an autosomal dominant condition characterized by a familial history of congenital heart defects and preaxial radial upper-limb defects. We report aberrant apoptosis and dormant ce...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-10-01
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Series: | Journal of Biomedical Science |
Subjects: | |
Online Access: | http://www.jbiomedsci.com/content/18/1/73 |