Papers associated with left (and rab40b)

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	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.
	Alteration of the Retinoid Acid-CBP Signaling Pathway in Neural Crest Induction Contributes to Enteric Nervous System Disorder., Li C., Front Pediatr. December 3, 2018; 6 382.
	Transcriptome analysis of Xenopus orofacial tissues deficient in retinoic acid receptor function., Wahl SE., BMC Genomics. November 3, 2018; 19 (1): 795.
	Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels., Chae S., Sci Rep. August 21, 2017; 7 (1): 8874.
	RARβ2 is required for vertebrate somitogenesis., Janesick A., Development. June 1, 2017; 144 (11): 1997-2008.
	The role of folate metabolism in orofacial development and clefting., Wahl SE., Dev Biol. September 1, 2015; 405 (1): 108-22.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	Retinoic acid induced-1 (Rai1) regulates craniofacial and brain development in Xenopus., Tahir R., Mech Dev. August 1, 2014; 133 91-104.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	Chemical activation of RARβ induces post-embryonically bilateral limb duplication during Xenopus limb regeneration., Cuervo R., Sci Rep. January 1, 2013; 3 1886.
	Analyzing the function of a hox gene: an evolutionary approach., Michaut L., Dev Growth Differ. December 1, 2011; 53 (9): 982-93.
	The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate., Li Y., J Biol Chem. December 4, 2009; 284 (49): 34283-95.
	Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis., Fierro AC., BMC Genomics. May 16, 2007; 8 118.
	Retinoic acid signalling is required for specification of pronephric cell fate., Cartry J., Dev Biol. November 1, 2006; 299 (1): 35-51.
	Neofunctionalization in vertebrates: the example of retinoic acid receptors., Escriva H., PLoS Genet. July 1, 2006; 2 (7): e102.
	Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
	The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development., Barreto G., Mech Dev. April 1, 2003; 120 (4): 415-28.
	Active repression of RAR signaling is required for head formation., Koide T., Genes Dev. August 15, 2001; 15 (16): 2111-21.
	Inhibition of retinoic acid receptor-mediated signalling alters positional identity in the developing hindbrain., van der Wees J., Development. February 1, 1998; 125 (3): 545-56.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H., Genes Dev. January 1, 1991; 5 (1): 94-104.

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