Papers associated with epidermis (and pitx2)

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	CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability., Deniz E., Dev Biol. July 1, 2023; 499 75-88.
	Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease., Mishra-Gorur K., Proc Natl Acad Sci U S A. April 18, 2023; 120 (16): e2214997120.
	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
	RNA demethylation by FTO stabilizes the FOXJ1 mRNA for proper motile ciliogenesis., Kim H., Dev Cell. April 19, 2021; 56 (8): 1118-1130.e6.
	Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.
	CFAP43 modulates ciliary beating in mouse and Xenopus., Rachev E., Dev Biol. March 15, 2020; 459 (2): 109-125.
	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.
	A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates., Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
	What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia., Walentek P., Genesis. January 1, 2017; 55 (1-2):
	Ciliary transcription factors and miRNAs precisely regulate Cp110 levels required for ciliary adhesions and ciliogenesis., Walentek P., Elife. September 13, 2016; 5
	Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia., Del Viso F., Dev Cell. September 12, 2016; 38 (5): 478-92.
	ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled., Miyatake K., Nat Commun. March 31, 2015; 6 6666.
	Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral-right blastomere., Tingler M., Genesis. June 1, 2014; 52 (6): 588-99.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	RFX2 is broadly required for ciliogenesis during vertebrate development., Chung MI., Dev Biol. March 1, 2012; 363 (1): 155-65.
	Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left-Right Asymmetry., Pai VP., Stem Cells Int. January 1, 2012; 2012 353491.
	Flow on the right side of the gastrocoel roof plate is dispensable for symmetry breakage in the frog Xenopus laevis., Vick P., Dev Biol. July 15, 2009; 331 (2): 281-91.
	Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination., Hilton EN., Hum Mol Genet. July 15, 2007; 16 (14): 1773-82.
	More than 95% reversal of left-right axis induced by right-sided hypodermic microinjection of activin into Xenopus neurula embryos., Toyoizumi R., Dev Biol. May 15, 2000; 221 (2): 321-36.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.

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