Papers associated with connective tissue (and nodal3.1)

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	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	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.
	NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling., Zhang Y., Dev Biol. August 1, 2014; 392 (1): 15-25.
	Calpain2 protease: A new member of the Wnt/Ca(2+) pathway modulating convergent extension movements in Xenopus., Zanardelli S., Dev Biol. December 1, 2013; 384 (1): 83-100.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells., Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	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.
	Vegetally localized Xenopus trim36 regulates cortical rotation and dorsal axis formation., Cuykendall TN., Development. September 1, 2009; 136 (18): 3057-65.
	Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Bone density ligand, Sclerostin, directly interacts with LRP5 but not LRP5G171V to modulate Wnt activity., Ellies DL., J Bone Miner Res. November 1, 2006; 21 (11): 1738-49.
	XIC is required for Siamois activity and dorsoanterior development., Snider L., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	A novel role for a nodal-related protein; Xnr3 regulates convergent extension movements via the FGF receptor., Yokota C., Development. May 1, 2003; 130 (10): 2199-212.
	Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.
	Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus., Smithers LE., Mech Dev. December 1, 2002; 119 (2): 191-200.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	The IGF pathway regulates head formation by inhibiting Wnt signaling in Xenopus., Richard-Parpaillon L., Dev Biol. April 15, 2002; 244 (2): 407-17.
	The role of maternal axin in patterning the Xenopus embryo., Kofron M., Dev Biol. September 1, 2001; 237 (1): 183-201.
	foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
	FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G., Dev Biol. December 15, 2000; 228 (2): 304-14.
	The Toll/IL-1 receptor binding protein MyD88 is required for Xenopus axis formation., Prothmann C., Mech Dev. October 1, 2000; 97 (1-2): 85-92.
	Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.
	Primary structure requirements for Xenopus nodal-related 3 and a comparison with regions required by Xenopus nodal-related 2., Ezal CH., J Biol Chem. May 12, 2000; 275 (19): 14124-31.
	Endodermal Nodal-related signals and mesoderm induction in Xenopus., Agius E., Development. March 1, 2000; 127 (6): 1173-83.
	Amphibian embryos as a model system for organ engineering: in vitro induction and rescue of the heart anlage., Grunz H., Int J Dev Biol. July 1, 1999; 43 (4): 361-4.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.
	Mutant Vg1 ligands disrupt endoderm and mesoderm formation in Xenopus embryos., Joseph EM., Development. July 1, 1998; 125 (14): 2677-85.
	Markers of vertebrate mesoderm induction., Stennard F., Curr Opin Genet Dev. October 1, 1997; 7 (5): 620-7.
	Combinatorial signalling by Xwnt-11 and Xnr3 in the organizer epithelium., Glinka A., Mech Dev. December 1, 1996; 60 (2): 221-31.
	Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S., Genes Dev. November 1, 1996; 10 (21): 2805-17.
	Blastomere derivation and domains of gene expression in the Spemann Organizer of Xenopus laevis., Vodicka MA., Development. November 1, 1995; 121 (11): 3505-18.

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