Papers associated with tail bud (and mst1)

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	Hippo signaling components, Mst1 and Mst2, act as a switch between self-renewal and differentiation in Xenopus hematopoietic and endothelial progenitors., Nejigane S., Int J Dev Biol. January 1, 2013; 57 (5): 407-14.
	The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
	A dual requirement for Iroquois genes during Xenopus kidney development., Alarcón P., Development. October 1, 2008; 135 (19): 3197-207.
	Xiro homeoproteins coordinate cell cycle exit and primary neuron formation by upregulating neuronal-fate repressors and downregulating the cell-cycle inhibitor XGadd45-gamma., de la Calle-Mustienes E., Mech Dev. November 1, 2002; 119 (1): 69-80.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	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.
	A member of the Met/HGF-receptor family is expressed in a BMP-4-like pattern in the ectoderm of Xenopus gastrulae., Aberger F., Biochem Biophys Res Commun. February 3, 1997; 231 (1): 191-5.
	Involvement of Livertine, a hepatocyte growth factor family member, in neural morphogenesis., Ruiz i Altaba A., Mech Dev. December 1, 1996; 60 (2): 207-20.
	Cloning and expression of Xenopus HGF-like protein (HLP) and Ron/HLP receptor implicate their involvement in early neural development., Nakamura T., Biochem Biophys Res Commun. July 16, 1996; 224 (2): 564-73.

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