Papers associated with process (and npat)

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	Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
	Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility., Robson A., Proc Natl Acad Sci U S A. July 9, 2019; 116 (28): 14049-14054.
	Evolution of the hypoxia-sensitive cells involved in amniote respiratory reflexes., Hockman D., Elife. April 7, 2017; 6
	Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
	Cadherin 2/4 signaling via PTP1B and catenins is crucial for nucleokinesis during radial neuronal migration in the neocortex., Martinez-Garay I., Development. June 15, 2016; 143 (12): 2121-34.
	Lung epithelial branching program antagonizes alveolar differentiation., Chang DR., Proc Natl Acad Sci U S A. November 5, 2013; 110 (45): 18042-51.
	Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice., Rainger J., PLoS Genet. July 1, 2011; 7 (7): e1002114.
	Developmental expression of retinoic acid receptors (RARs)., Dollé P., Nucl Recept Signal. May 12, 2009; 7 e006.
	Expression study of cadherin7 and cadherin20 in the embryonic and adult rat central nervous system., Takahashi M., BMC Dev Biol. June 23, 2008; 8 87.
	Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome., Dagenais SL., Gene Expr Patterns. October 1, 2004; 4 (6): 611-9.

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