Papers associated with tail region (and hoxa9)

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	Retinoic acid can mimic endogenous signals involved in transformation of the Xenopus nervous system., Sharpe CR., Neuron. August 1, 1991; 7 (2): 239-47.
	A Xenopus borealis homeobox gene expressed preferentially in posterior ectoderm., Stickland JE., Gene. July 15, 1992; 116 (2): 269-73.
	Overexpression of a cellular retinoic acid binding protein (xCRABP) causes anteroposterior defects in developing Xenopus embryos., Dekker EJ., Development. April 1, 1994; 120 (4): 973-85.
	Caudalization of neural fate by tissue recombination and bFGF., Cox WG., Development. December 1, 1995; 121 (12): 4349-58.
	Disruption of BMP signals in embryonic Xenopus ectoderm leads to direct neural induction., Hawley SH., Genes Dev. December 1, 1995; 9 (23): 2923-35.
	Xenopus mothers against decapentaplegic is an embryonic ventralizing agent that acts downstream of the BMP-2/4 receptor., Thomsen GH., Development. August 1, 1996; 122 (8): 2359-66.
	A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME., Development. May 1, 1997; 124 (9): 1689-98.
	Xenopus Zic3, a primary regulator both in neural and neural crest development., Nakata K., Proc Natl Acad Sci U S A. October 28, 1997; 94 (22): 11980-5.
	Expression of Xfz3, a Xenopus frizzled family member, is restricted to the early nervous system., Shi DL., Mech Dev. January 1, 1998; 70 (1-2): 35-47.
	Midkine counteracts the activin signal in mesoderm induction and promotes neural formation., Yokota C., J Biochem. February 1, 1998; 123 (2): 339-46.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	Post-transcriptional regulation of Xwnt-8 expression is required for normal myogenesis during vertebrate embryonic development., Tian Q., Development. August 1, 1999; 126 (15): 3371-80.
	Abdominal B-type Hox gene expression in Xenopus laevis., Lombardo A., Mech Dev. August 1, 2001; 106 (1-2): 191-5.
	FoxI1e activates ectoderm formation and controls cell position in the Xenopus blastula., Mir A., Development. February 1, 2007; 134 (4): 779-88.
	Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis., Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.
	The RING finger protein MSL2 in the MOF complex is an E3 ubiquitin ligase for H2B K34 and is involved in crosstalk with H3 K4 and K79 methylation., Wu L., Mol Cell. July 8, 2011; 43 (1): 132-44.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Morphological and transcriptomic analyses reveal three discrete primary stages of postembryonic development in the common fire salamander, Salamandra salamandra., Sanchez E., J Exp Zool B Mol Dev Evol. March 1, 2018; 330 (2): 96-108.
	Tril dampens Nodal signaling through Pellino2- and Traf6-mediated activation of Nedd4l., Kim HS., Proc Natl Acad Sci U S A. September 7, 2021; 118 (36):
	Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH., Dev Biol. March 1, 2022; 483 157-168.

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