Papers associated with tail (and hoxb9)

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	The cytokine FAM3B/PANDER is an FGFR ligand that promotes posterior development in Xenopus., Zhang F., Proc Natl Acad Sci U S A. May 18, 2021; 118 (20):
	What are the roles of retinoids, other morphogens, and Hox genes in setting up the vertebrate body axis?, Durston AJ., Genesis. July 1, 2019; 57 (7-8): e23296.
	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	β-Adrenergic signaling promotes posteriorization in Xenopus early development., Mori S., Dev Growth Differ. April 1, 2013; 55 (3): 350-8.
	xCITED2 Induces Neural Genes in Animal Cap Explants of Xenopus Embryos., Yoon J., Exp Neurobiol. September 1, 2011; 20 (3): 123-9.
	Focal adhesion kinase protein regulates Wnt3a gene expression to control cell fate specification in the developing neural plate., Fonar Y., Mol Biol Cell. July 1, 2011; 22 (13): 2409-21.
	Histone XH2AX is required for Xenopus anterior neural development: critical role of threonine 16 phosphorylation., Lee SY., J Biol Chem. September 17, 2010; 285 (38): 29525-34.
	The RNA-binding protein Seb4/RBM24 is a direct target of MyoD and is required for myogenesis during Xenopus early development., Li HY., Mech Dev. January 1, 2010; 127 (5-6): 281-91.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	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.
	VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development., Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.
	The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	FGF8, Wnt8 and Myf5 are target genes of Tbx6 during anteroposterior specification in Xenopus embryo., Li HY., Dev Biol. February 15, 2006; 290 (2): 470-81.
	Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.
	Conserved cross-interactions in Drosophila and Xenopus between Ras/MAPK signaling and the dual-specificity phosphatase MKP3., Gómez AR., Dev Dyn. March 1, 2005; 232 (3): 695-708.
	Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.
	Twisted gastrulation loss-of-function analyses support its role as a BMP inhibitor during early Xenopus embryogenesis., Blitz IL., Development. October 1, 2003; 130 (20): 4975-88.
	Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.
	Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos., Oelgeschläger M., Dev Cell. February 1, 2003; 4 (2): 219-30.
	Anteroposterior patterning in Xenopus embryos: egg fragment assay system reveals a synergy of dorsalizing and posteriorizing embryonic domains., Fujii H., Dev Biol. December 1, 2002; 252 (1): 15-30.
	The latent-TGFbeta-binding-protein-1 (LTBP-1) is expressed in the organizer and regulates nodal and activin signaling., Altmann CR., Dev Biol. August 1, 2002; 248 (1): 118-27.
	Xenopus Dishevelled signaling regulates both neural and mesodermal convergent extension: parallel forces elongating the body axis., Wallingford JB., Development. July 1, 2001; 128 (13): 2581-92.
	Expression of activated MAP kinase in Xenopus laevis embryos: evaluating the roles of FGF and other signaling pathways in early induction and patterning., Curran KL., Dev Biol. December 1, 2000; 228 (1): 41-56.
	Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.
	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.
	Evidence for non-axial A/P patterning in the nonneural ectoderm of Xenopus and zebrafish pregastrula embryos., Read EM., Int J Dev Biol. September 1, 1998; 42 (6): 763-74.
	Two phases of Hox gene regulation during early Xenopus development., Pownall ME., Curr Biol. May 21, 1998; 8 (11): 673-6.
	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.
	The Spemann organizer of Xenopus is patterned along its anteroposterior axis at the earliest gastrula stage., Zoltewicz JS., Dev Biol. December 15, 1997; 192 (2): 482-91.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	eFGF, Xcad3 and Hox genes form a molecular pathway that establishes the anteroposterior axis in Xenopus., Pownall ME., Development. December 1, 1996; 122 (12): 3881-92.
	Expression patterns of Hoxb genes in the Xenopus embryo suggest roles in anteroposterior specification of the hindbrain and in dorsoventral patterning of the mesoderm., Godsave S., Dev Biol. December 1, 1994; 166 (2): 465-76.
	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.

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