Papers associated with left (and slc45a2)

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	Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders., Kaiyrzhanov R., Brain. April 4, 2024; 147 (4): 1436-1456.
	Revealing mitf functions and visualizing allografted tumor metastasis in colorless and immunodeficient Xenopus tropicalis., Ran R., Commun Biol. March 5, 2024; 7 (1): 275.
	HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes., Grand K., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.
	Hnf1b renal expression directed by a distal enhancer responsive to Pax8., Goea L., Sci Rep. November 19, 2022; 12 (1): 19921.
	A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.
	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):
	Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders., Wyatt BH., Genesis. February 1, 2021; 59 (1-2): e23394.
	The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos., Willsey HR., Development. June 22, 2020; 147 (21):
	Simple embryo injection of long single-stranded donor templates with the CRISPR/Cas9 system leads to homology-directed repair in Xenopus tropicalis and Xenopus laevis., Nakayama T., Genesis. June 1, 2020; 58 (6): e23366.
	Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development., DeLay BD., Front Physiol. January 1, 2019; 10 143.
	Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos., Willsey HR., Dev Biol. October 15, 2018; 442 (2): 276-287.

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