Papers associated with vein (and tbx2)

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	Endogenous gradients of resting potential instructively pattern embryonic neural tissue via Notch signaling and regulation of proliferation., Pai VP., J Neurosci. March 11, 2015; 35 (10): 4366-85.
	MiR-142-3p controls the specification of definitive hemangioblasts during ontogeny., Nimmo R., Dev Cell. August 12, 2013; 26 (3): 237-49.
	Uncoupling VEGFA functions in arteriogenesis and hematopoietic stem cell specification., Leung A., Dev Cell. January 28, 2013; 24 (2): 144-58.
	A large scale screen for neural stem cell markers in Xenopus retina., Parain K., Dev Neurobiol. April 1, 2012; 72 (4): 491-506.
	The spatio-temporal expression of ProSAP/shank family members and their interaction partner LAPSER1 during Xenopus laevis development., Gessert S., Dev Dyn. June 1, 2011; 240 (6): 1528-36.
	Programming pluripotent precursor cells derived from Xenopus embryos to generate specific tissues and organs., Borchers A., Genes (Basel). November 18, 2010; 1 (3): 413-26.
	Claudin-like protein 24 interacts with the VEGFR-2 and VEGFR-3 pathways and regulates lymphatic vessel development., Saharinen P., Genes Dev. May 1, 2010; 24 (9): 875-80.
	The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Expression of complement components coincides with early patterning and organogenesis in Xenopus laevis., McLin VA., Int J Dev Biol. January 1, 2008; 52 (8): 1123-33.
	Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo., Cox CM., Dev Biol. August 1, 2006; 296 (1): 177-89.
	GABAergic specification in the basal forebrain is controlled by the LIM-hd factor Lhx7., Bachy I., Dev Biol. March 15, 2006; 291 (2): 218-26.
	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.
	Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.
	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.
	Endoderm is required for vascular endothelial tube formation, but not for angioblast specification., Vokes SA., Development. February 1, 2002; 129 (3): 775-85.
	Vascular control in larval Xenopus laevis: the role of endothelial-derived factors., Schwerte T., J Exp Biol. January 1, 2002; 205 (Pt 2): 225-32.
	VEGF mediates angioblast migration during development of the dorsal aorta in Xenopus., Cleaver O., Development. October 1, 1998; 125 (19): 3905-14.
	An essential role for retinoid signaling in anteroposterior neural patterning., Blumberg B., Development. January 1, 1997; 124 (2): 373-9.
	Control of melanoblast differentiation in amphibia by alpha-melanocyte stimulating hormone, a serum melanization factor, and a melanization inhibiting factor., Fukuzawa T., Pigment Cell Res. January 1, 1989; 2 (3): 171-81.

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