Papers associated with process (and snai1)

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	TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):
	Cell landscape of larval and adult Xenopus laevis at single-cell resolution., Liao Y., Nat Commun. July 25, 2022; 13 (1): 4306.
	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):
	Foxm1 regulates neural progenitor fate during spinal cord regeneration., Pelzer D., EMBO Rep. September 6, 2021; 22 (9): e50932.
	Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates., Bright AR., EMBO J. May 3, 2021; 40 (9): e104913.
	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
	Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.
	The transcription factor Sox9 is required for cranial neural crest development in Xenopus., Spokony RF., Development. January 1, 2002; 129 (2): 421-32.

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