Papers associated with tadpole (and sox17a)

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	Cell landscape of larval and adult Xenopus laevis at single-cell resolution., Liao Y., Nat Commun. July 25, 2022; 13 (1): 4306.
	Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):
	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.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	Regulation of nuclear-cytoplasmic shuttling and function of Family with sequence similarity 13, member A (Fam13a), by B56-containing PP2As and Akt., Jin Z., Mol Biol Cell. March 15, 2015; 26 (6): 1160-73.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Sirtuin inhibitor Ex-527 causes neural tube defects, ventral edema formations, and gastrointestinal malformations in Xenopus laevis embryos., Ohata Y., Dev Growth Differ. August 1, 2014; 56 (6): 460-8.
	Pou-V factor Oct25 regulates early morphogenesis in Xenopus laevis., Julier A., Dev Growth Differ. September 1, 2012; 54 (7): 702-16.
	A developmental requirement for HIRA-dependent H3.3 deposition revealed at gastrulation in Xenopus., Szenker E., Cell Rep. June 28, 2012; 1 (6): 730-40.
	The roles of maternal Vangl2 and aPKC in Xenopus oocyte and embryo patterning., Cha SW., Development. September 1, 2011; 138 (18): 3989-4000.
	Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53., Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
	Expression of Sox1 during Xenopus early embryogenesis., Nitta KR., Biochem Biophys Res Commun. December 8, 2006; 351 (1): 287-93.
	The RNA-binding protein, Vg1RBP, is required for pancreatic fate specification., Spagnoli FM., Dev Biol. April 15, 2006; 292 (2): 442-56.
	The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C., Development. October 1, 2005; 132 (20): 4575-86.
	Xenopus ILK (integrin-linked kinase) is required for morphogenetic movements during gastrulation., Yasunaga T., Genes Cells. April 1, 2005; 10 (4): 369-79.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	Patterning and tissue movements in a novel explant preparation of the marginal zone of Xenopus laevis., Davidson LA., Gene Expr Patterns. July 1, 2004; 4 (4): 457-66.
	Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants., Latinkić BV., Development. August 1, 2003; 130 (16): 3865-76.
	Mutual antagonism between dickkopf1 and dickkopf2 regulates Wnt/beta-catenin signalling., Wu W., Curr Biol. December 1, 2000; 10 (24): 1611-4.
	Mesendoderm induction and reversal of left-right pattern by mouse Gdf1, a Vg1-related gene., Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.

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