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Jeffrey C. Murray, Brian C. Schutte
J Clin Invest. 2004;
113(12):1676
doi:10.1172/JCI22154
Abstract |
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left lip and palate is a common human birth defect, and its causes are being dissected through studies of human populations and through the use of animal models. Mouse models in particular have made a substantial contribution to our understanding of the gene pathways involved in palate development and the nature of signaling molecules that act in a tissue-specific manner at critical stages of embryogenesis. Related work has provided further support for investigating the role of common environmental triggers as causal covariates.
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(18)
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Eur. J. Hum. Genet.
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J Anatomy
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2008 |
Follistatin antagonizes transforming growth factor-β3-induced epithelial–mesenchymal transition in vitro: implications for murine palatal development supported by microarray analysis
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Differentiation
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TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.
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Am. J. Hum. Genet.
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2007 |
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Regional heterogeneity in the developing palate: morphological and molecular evidence for normal and abnormal palatogenesis
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Dev. Dyn.
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