Papers associated with cranium (and npat)

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	Systematic mapping of rRNA 2'-O methylation during frog development and involvement of the methyltransferase Fibrillarin in eye and craniofacial development in Xenopus laevis., Delhermite J., PLoS Genet. January 18, 2022; 18 (1): e1010012.
	Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
	Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis., Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.
	Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarity., Escobedo N., Development. July 1, 2013; 140 (14): 3008-17.
	Transcriptional activation by Oct4 is sufficient for the maintenance and induction of pluripotency., Hammachi F., Cell Rep. February 23, 2012; 1 (2): 99-109.
	Identification of the pre-T-cell receptor alpha chain in nonmammalian vertebrates challenges the structure-function of the molecule., Smelty P., Proc Natl Acad Sci U S A. November 16, 2010; 107 (46): 19991-6.
	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.

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