Papers associated with tail bud (and vegfa)

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	HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes., Grand K., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.
	Nodal signalling in Xenopus: the role of Xnr5 in left/right asymmetry and heart development., Tadjuidje E., Open Biol. August 1, 2016; 6 (8):
	Expression and localization of Rdd proteins in Xenopus embryo., Lim JC., Anat Cell Biol. March 1, 2014; 47 (1): 18-27.
	A transgenic Xenopus laevis reporter model to study lymphangiogenesis., Ny A., Biol Open. July 11, 2013; 2 (9): 882-90.
	A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling., Peyrot SM., Dev Biol. April 15, 2011; 352 (2): 254-66.
	Isthmin is a novel secreted angiogenesis inhibitor that inhibits tumour growth in mice., Xiang W., J Cell Mol Med. February 1, 2011; 15 (2): 359-74.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development., Kazanskaya O., Development. November 1, 2008; 135 (22): 3655-64.
	Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
	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.
	VEGF mediates angioblast migration during development of the dorsal aorta in Xenopus., Cleaver O., Development. October 1, 1998; 125 (19): 3905-14.
	Neovascularization of the Xenopus embryo., Cleaver O., Dev Dyn. September 1, 1997; 210 (1): 66-77.

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