Papers associated with primary germ layer (and hoxa1)

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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.
	Genetically programmed retinoic acid deficiency during gastrulation phenocopies most known developmental defects due to acute prenatal alcohol exposure in FASD., Petrelli B., Front Cell Dev Biol. January 1, 2023; 11 1208279.
	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.
	Reduced Retinoic Acid Signaling During Gastrulation Induces Developmental Microcephaly., Gur M., Front Cell Dev Biol. January 1, 2022; 10 844619.
	Chromatin accessibility and histone acetylation in the regulation of competence in early development., Esmaeili M., Dev Biol. June 1, 2020; 462 (1): 20-35.
	RARγ is required for mesodermal gene expression prior to gastrulation in Xenopus., Janesick A., Development. September 17, 2018; 145 (18):
	Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis., Gere-Becker MB., Development. June 8, 2018; 145 (12):
	Acetaldehyde inhibits retinoic acid biosynthesis to mediate alcohol teratogenicity., Shabtai Y., Sci Rep. January 10, 2018; 8 (1): 347.
	Genome-wide identification of Wnt/β-catenin transcriptional targets during Xenopus gastrulation., Kjolby RAS., Dev Biol. June 15, 2017; 426 (2): 165-175.
	ADHFe1: a novel enzyme involved in retinoic acid-dependent Hox activation., Shabtai Y., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 303-310.
	Tissue- and stage-specific Wnt target gene expression is controlled subsequent to β-catenin recruitment to cis-regulatory modules., Nakamura Y., Development. June 1, 2016; 143 (11): 1914-25.
	Noggin4 is a long-range inhibitor of Wnt8 signalling that regulates head development in Xenopus laevis., Eroshkin FM., Sci Rep. January 22, 2016; 6 23049.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Epigenetic modification maintains intrinsic limb-cell identity in Xenopus limb bud regeneration., Hayashi S., Dev Biol. October 15, 2015; 406 (2): 271-82.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	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.
	Hox and Pbx factors control retinoic acid synthesis during hindbrain segmentation., Vitobello A., Dev Cell. April 19, 2011; 20 (4): 469-82.
	Xwnt8 directly initiates expression of labial Hox genes., In der Rieden PM., Dev Dyn. January 1, 2010; 239 (1): 126-39.
	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.
	Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.
	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.
	Identification of genes induced in regenerating Xenopus tadpole tails by using the differential display method., Ishino T., Dev Dyn. February 1, 2003; 226 (2): 317-25.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Regulation of the Xenopus labial homeodomain genes, HoxA1 and HoxD1: activation by retinoids and peptide growth factors., Kolm PJ., Dev Biol. January 1, 1995; 167 (1): 34-49.
	Retinoic acid perturbs the expression of Xhox.lab genes and alters mesodermal determination in Xenopus laevis., Sive HL., Genes Dev. August 1, 1991; 5 (8): 1321-32.

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