Papers associated with tail bud (and lgals4.2)

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	Caspase-9 has a nonapoptotic function in Xenopus embryonic primitive blood formation., Tran HT., J Cell Sci. July 15, 2017; 130 (14): 2371-2381.
	The Inner Nuclear Membrane Protein Nemp1 Is a New Type of RanGTP-Binding Protein in Eukaryotes., Shibano T., PLoS One. May 6, 2015; 10 (5): e0127271.
	β-Catenin-independent activation of TCF1/LEF1 in human hematopoietic tumor cells through interaction with ATF2 transcription factors., Grumolato L., PLoS Genet. January 1, 2013; 9 (8): e1003603.
	Mef2d acts upstream of muscle identity genes and couples lateral myogenesis to dermomyotome formation in Xenopus laevis., Della Gaspera B., PLoS One. January 1, 2012; 7 (12): e52359.
	Xenopus Dbx2 is involved in primary neurogenesis and early neural plate patterning., Ma P., Biochem Biophys Res Commun. August 19, 2011; 412 (1): 170-4.
	Conservation and diversification of an ancestral chordate gene regulatory network for dorsoventral patterning., Kozmikova I., PLoS One. February 3, 2011; 6 (2): e14650.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	Xenopus galectin-VIa shows highly specific expression in cement glands and is regulated by canonical Wnt signaling., Michiue T., Gene Expr Patterns. October 1, 2007; 7 (8): 852-7.
	Neofunctionalization in vertebrates: the example of retinoic acid receptors., Escriva H., PLoS Genet. July 1, 2006; 2 (7): e102.
	XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.
	MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.
	Sequences downstream of the bHLH domain of the Xenopus hairy-related transcription factor-1 act as an extended dimerization domain that contributes to the selection of the partners., Taelman V., Dev Biol. December 1, 2004; 276 (1): 47-63.
	Characterization of the Xenopus galectin family. Three structurally different types as in mammals and regulated expression during embryogenesis., Shoji H., J Biol Chem. April 4, 2003; 278 (14): 12285-93.
	Identification of putative interaction partners for the Xenopus Polycomb-group protein Xeed., Showell C., Gene. May 29, 2002; 291 (1-2): 95-104.
	FOR, a novel orphan nuclear receptor related to farnesoid X receptor., Seo YW., J Biol Chem. May 17, 2002; 277 (20): 17836-44.
	Isolation and characterization of XKaiso, a transcriptional repressor that associates with the catenin Xp120(ctn) in Xenopus laevis., Kim SW., J Biol Chem. March 8, 2002; 277 (10): 8202-8.
	Hes6 acts in a positive feedback loop with the neurogenins to promote neuronal differentiation., Koyano-Nakagawa N., Development. October 1, 2000; 127 (19): 4203-16.
	Regulation of Wnt signaling by Sox proteins: XSox17 alpha/beta and XSox3 physically interact with beta-catenin., Zorn AM., Mol Cell. October 1, 1999; 4 (4): 487-98.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.
	A role for Xenopus Gli-type zinc finger proteins in the early embryonic patterning of mesoderm and neuroectoderm., Marine JC., Mech Dev. May 1, 1997; 63 (2): 211-25.

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