Papers associated with lateral (and cyp26a1)

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	Retinoic acid control of pax8 during renal specification of Xenopus pronephros involves hox and meis3., Durant-Vesga J., Dev Biol. January 1, 2023; 493 17-28.
	Reduced Retinoic Acid Signaling During Gastrulation Induces Developmental Microcephaly., Gur M., Front Cell Dev Biol. January 1, 2022; 10 844619.
	Retinol binding protein 1 affects Xenopus anterior neural development via all-trans retinoic acid signaling., Flach H., Dev Dyn. August 1, 2021; 250 (8): 1096-1112.
	Embryonic Epidermal Lectins in Three Amphibian Species, Rana ornativentris, Bufo japonicus formosus, and Cynops pyrrhogaster., Nagata S., Zoolog Sci. August 1, 2020; 37 (4): 338-345.
	On-Site Ribosome Remodeling by Locally Synthesized Ribosomal Proteins in Axons., Shigeoka T., Cell Rep. December 10, 2019; 29 (11): 3605-3619.e10.
	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.
	Timing is everything: Reiterative Wnt, BMP and RA signaling regulate developmental competence during endoderm organogenesis., Rankin SA, Rankin SA., Dev Biol. February 1, 2018; 434 (1): 121-132.
	Visualization of Gene Expression Patterns by In Situ Hybridization on Early Stages of Development of Xenopus laevis., El-Hodiri HM., Methods Mol Biol. January 1, 2018; 1797 325-335.
	Tumor protein Tctp regulates axon development in the embryonic visual system., Roque CG., Development. April 1, 2016; 143 (7): 1134-48.
	Xenopus Limb bud morphogenesis., Keenan SR., Dev Dyn. March 1, 2016; 245 (3): 233-43.
	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.
	Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus., Thélie A., Development. October 1, 2015; 142 (19): 3416-28.
	Rdh10a Provides a Conserved Critical Step in the Synthesis of Retinoic Acid during Zebrafish Embryogenesis., D'Aniello E., PLoS One. September 1, 2015; 10 (9): e0138588.
	TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus., Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.
	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.
	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.
	A gene regulation network controlled by Celf1 protein-rbpj mRNA interaction in Xenopus somite segmentation., Cibois M., Biol Open. August 21, 2013; 2 (10): 1078-83.
	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.
	Chemical activation of RARβ induces post-embryonically bilateral limb duplication during Xenopus limb regeneration., Cuervo R., Sci Rep. January 1, 2013; 3 1886.
	Retinoic acid-dependent control of MAP kinase phosphatase-3 is necessary for early kidney development in Xenopus., Le Bouffant R., Biol Cell. September 1, 2012; 104 (9): 516-32.
	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.
	Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration., Love NR., BMC Dev Biol. November 15, 2011; 11 70.
	Expression of key retinoic acid modulating genes suggests active regulation during development and regeneration of the amphibian limb., McEwan J., Dev Dyn. May 1, 2011; 240 (5): 1259-70.
	Analysis of the expression of retinoic acid metabolising genes during Xenopus laevis organogenesis., Lynch J., Gene Expr Patterns. January 1, 2011; 11 (1-2): 112-7.
	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.
	The efficiency of Xenopus primordial germ cell migration depends on the germplasm mRNA encoding the PDZ domain protein Grip2., Kirilenko P., Differentiation. April 1, 2008; 76 (4): 392-403.
	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.
	The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros., Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.
	Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.
	Retinoic acid signalling is required for specification of pronephric cell fate., Cartry J., Dev Biol. November 1, 2006; 299 (1): 35-51.
	Role for retinoid signaling in left-right asymmetric digestive organ morphogenesis., Lipscomb K., Dev Dyn. August 1, 2006; 235 (8): 2266-75.
	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 Meis3 protein and retinoid signaling interact to pattern the Xenopus hindbrain., Dibner C., Dev Biol. July 1, 2004; 271 (1): 75-86.
	Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation., Shiotsugu J., Development. June 1, 2004; 131 (11): 2653-67.
	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.
	PKCgamma regulates syndecan-2 inside-out signaling during xenopus left-right development., Kramer KL., Cell. December 27, 2002; 111 (7): 981-90.
	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.
	Increased XRALDH2 activity has a posteriorizing effect on the central nervous system of Xenopus embryos., Chen Y., Mech Dev. March 1, 2001; 101 (1-2): 91-103.
	Structure, biological activity of the upstream regulatory sequence, and conserved domains of a middle molecular mass neurofilament gene of Xenopus laevis., Roosa JR., Brain Res Mol Brain Res. October 20, 2000; 82 (1-2): 35-51.

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