Papers associated with neuroectoderm (and cyp26a1)

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	Alcohol induces neural tube defects by reducing retinoic acid signaling and promoting neural plate expansion., Edri T., Front Cell Dev Biol. January 1, 2023; 11 1282273.
	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.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.
	Development of the vertebrate tailbud., Beck CW., Wiley Interdiscip Rev Dev Biol. January 1, 2015; 4 (1): 33-44.
	Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	Retinoic acid regulation by CYP26 in vertebrate lens regeneration., Thomas AG., Dev Biol. February 15, 2014; 386 (2): 291-301.
	Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	Expression of Ski can act as a negative feedback mechanism on retinoic acid signaling., Melling MA., Dev Dyn. June 1, 2013; 242 (6): 604-13.
	A hindbrain-repressive Wnt3a/Meis3/Tsh1 circuit promotes neuronal differentiation and coordinates tissue maturation., Elkouby YM., Development. April 1, 2012; 139 (8): 1487-97.
	xCOUP-TF-B regulates xCyp26 transcription and modulates retinoic acid signaling for anterior neural patterning in Xenopus., Tanibe M., Int J Dev Biol. January 1, 2012; 56 (4): 239-44.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.
	Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.
	Retinoic acid regulates anterior-posterior patterning within the lateral plate mesoderm of Xenopus., Deimling SJ., Mech Dev. October 1, 2009; 126 (10): 913-23.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis., Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.
	Control of kidney, eye and limb expression of Bmp7 by an enhancer element highly conserved between species., Adams D., Dev Biol. November 15, 2007; 311 (2): 679-90.
	Gene expression in Xenopus laevis embryos after Triadimefon exposure., Papis E., Gene Expr Patterns. January 1, 2007; 7 (1-2): 137-42.
	Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
	Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction., Monsoro-Burq AH., Dev Cell. February 1, 2005; 8 (2): 167-78.
	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.
	Isolation and characterization of a Xenopus gene (XMLP) encoding a MARCKS-like protein., Zhao H., Int J Dev Biol. October 1, 2001; 45 (7): 817-26.
	A gene trap approach in Xenopus., Bronchain OJ., Curr Biol. October 21, 1999; 9 (20): 1195-8.
	Immediate upstream sequence of arrestin directs rod-specific expression in Xenopus., Mani SS., J Biol Chem. May 28, 1999; 274 (22): 15590-7.
	Expression of retinoic acid 4-hydroxylase (CYP26) during mouse and Xenopus laevis embryogenesis., de Roos K., Mech Dev. April 1, 1999; 82 (1-2): 205-11.
	Regionalized metabolic activity establishes boundaries of retinoic acid signalling., Hollemann T., EMBO J. December 15, 1998; 17 (24): 7361-72.
	[An analysis of the expression of the genes containing the LeR-1 and VeR-1 sequences in the embryogenesis, regeneration and in the intact tissues of newts]., Markitantova IuV., Ontogenez. January 1, 1997; 28 (4): 262-70.

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