Papers associated with dorsal aorta

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	The distribution of fibronectin and tenascin along migratory pathways of the neural crest in the trunk of amphibian embryos., Epperlein HH., Development. August 1, 1988; 103 (4): 743-56.
	Ontogeny and tissue distribution of leukocyte-common antigen bearing cells during early development of Xenopus laevis., Ohinata H., Development. November 1, 1989; 107 (3): 445-52.
	Vital dye labelling of Xenopus laevis trunk neural crest reveals multipotency and novel pathways of migration., Collazo A., Development. June 1, 1993; 118 (2): 363-76.
	[Ontogeny of the pronephros and mesonephros in the South African clawed frog, Xenopus laevis Daudin, with special reference to the appearance and movement of the renin-immunopositive cells]., Tahara T., Jikken Dobutsu. October 1, 1993; 42 (4): 601-10.
	Expression of a new G protein-coupled receptor X-msr is associated with an endothelial lineage in Xenopus laevis., Devic E., Mech Dev. October 1, 1996; 59 (2): 129-40.
	Neovascularization of the Xenopus embryo., Cleaver O., Dev Dyn. September 1, 1997; 210 (1): 66-77.
	VEGF mediates angioblast migration during development of the dorsal aorta in Xenopus., Cleaver O., Development. October 1, 1998; 125 (19): 3905-14.
	Elucidating the origins of the vascular system: a fate map of the vascular endothelial and red blood cell lineages in Xenopus laevis., Mills KR., Dev Biol. May 15, 1999; 209 (2): 352-68.
	Response kinetics and pharmacological properties of heteromeric receptors formed by coassembly of GABA rho- and gamma 2-subunits., Qian H., Proc Biol Sci. December 7, 1999; 266 (1436): 2419-25.
	Endoderm patterning by the notochord: development of the hypochord in Xenopus., Cleaver O., Development. February 1, 2000; 127 (4): 869-79.
	Distinct origins of adult and embryonic blood in Xenopus., Ciau-Uitz A., Cell. September 15, 2000; 102 (6): 787-96.
	Isolation and expression analysis of three zebrafish angiopoietin genes., Pham VN., Dev Dyn. August 1, 2001; 221 (4): 470-4.
	Induction of pancreatic differentiation by signals from blood vessels., Lammert E., Science. October 19, 2001; 294 (5542): 564-7.
	Endoderm is required for vascular endothelial tube formation, but not for angioblast specification., Vokes SA., Development. February 1, 2002; 129 (3): 775-85.
	Primitive and definitive blood share a common origin in Xenopus: a comparison of lineage techniques used to construct fate maps., Lane MC., Dev Biol. August 1, 2002; 248 (1): 52-67.
	Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus., Walmsley M., Development. December 1, 2002; 129 (24): 5683-95.
	A trial for induction of supernumerary primordial germ cells in Xenopus tadpoles by injecting RNA of Xenopus vasa homologue into germline cells of 32-cell embryos., Ikenishi K., Dev Growth Differ. January 1, 2003; 45 (5-6): 417-26.
	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.
	Commentary: the role of cell migration in the ontogeny of the lymphoid system., Moore MA., Stem Cells Dev. February 1, 2004; 13 (1): 1-21.
	Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome., Dagenais SL., Gene Expr Patterns. October 1, 2004; 4 (6): 611-9.
	A vertebrate crossveinless 2 homologue modulates BMP activity and neural crest cell migration., Coles E., Development. November 1, 2004; 131 (21): 5309-17.
	The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development., Seo S., Dev Biol. June 15, 2006; 294 (2): 458-70.
	A novel gene, Ami is expressed in vascular tissue in Xenopus laevis., Inui M., Gene Expr Patterns. August 1, 2006; 6 (6): 613-9.
	The Xdsg protein in presumptive primordial germ cells (pPGCs) is essential to their differentiation into PGCs in Xenopus., Ikenishi K., Dev Biol. September 15, 2006; 297 (2): 483-92.
	Organization of the pronephric kidney revealed by large-scale gene expression mapping., Raciti D., Genome Biol. January 1, 2008; 9 (5): R84.
	Expression of the novel gene Ened during mouse and Xenopus embryonic development., Meszaros R., Int J Dev Biol. January 1, 2008; 52 (8): 1119-22.
	A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development., Rodrigues CO., Development. June 1, 2008; 135 (11): 1903-11.
	Expression study of cadherin7 and cadherin20 in the embryonic and adult rat central nervous system., Takahashi M., BMC Dev Biol. June 23, 2008; 8 87.
	Induction and modulation of smooth muscle differentiation in Xenopus embryonic cells., Barillot W., Dev Dyn. November 1, 2008; 237 (11): 3373-86.
	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.
	A reverse genetic screen in the zebrafish identifies crb2b as a regulator of the glomerular filtration barrier., Ebarasi L., Dev Biol. October 1, 2009; 334 (1): 1-9.
	Genetic control of hematopoietic development in Xenopus and zebrafish., Ciau-Uitz A., Int J Dev Biol. January 1, 2010; 54 (6-7): 1139-49.
	Tel1/ETV6 specifies blood stem cells through the agency of VEGF signaling., Ciau-Uitz A., Dev Cell. April 20, 2010; 18 (4): 569-78.
	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.
	HoxA3 is an apical regulator of haemogenic endothelium., Iacovino M., Nat Cell Biol. January 1, 2011; 13 (1): 72-8.
	Hedgehog signaling regulates size of the dorsal aortae and density of the plexus during avian vascular development., Moran CM., Dev Dyn. June 1, 2011; 240 (6): 1354-64.
	WD repeat-containing protein 5, a ubiquitously expressed histone methyltransferase adaptor protein, regulates smooth muscle cell-selective gene activation through interaction with pituitary homeobox 2., Gan Q., J Biol Chem. June 17, 2011; 286 (24): 21853-64.
	Transcription factor COUP-TFII is indispensable for venous and lymphatic development in zebrafish and Xenopus laevis., Aranguren XL., Biochem Biophys Res Commun. June 24, 2011; 410 (1): 121-6.
	Germ plasm in Eleutherodactylus coqui, a direct developing frog with large eggs., Elinson RP., Evodevo. October 6, 2011; 2 20.
	Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration., Love NR., BMC Dev Biol. November 15, 2011; 11 70.
	Activity-based labeling of matrix metalloproteinases in living vertebrate embryos., Keow JY., PLoS One. January 1, 2012; 7 (8): e43434.
	Uncoupling VEGFA functions in arteriogenesis and hematopoietic stem cell specification., Leung A., Dev Cell. January 28, 2013; 24 (2): 144-58.
	Amputation-induced reactive oxygen species are required for successful Xenopus tadpole tail regeneration., Love NR., Nat Cell Biol. February 1, 2013; 15 (2): 222-8.
	VEGFA-dependent and -independent pathways synergise to drive Scl expression and initiate programming of the blood stem cell lineage in Xenopus., Ciau-Uitz A., Development. June 1, 2013; 140 (12): 2632-42.
	A transgenic Xenopus laevis reporter model to study lymphangiogenesis., Ny A., Biol Open. July 11, 2013; 2 (9): 882-90.
	Xenopus cadherin 5 is specifically expressed in endothelial cells of the developing vascular system., Neuhaus H., Int J Dev Biol. January 1, 2014; 58 (1): 51-6.
	Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.
	Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
	Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos., Chatfield J., Development. June 1, 2014; 141 (12): 2429-40.
	Vangl-dependent planar cell polarity signalling is not required for neural crest migration in mammals., Pryor SE., Development. August 1, 2014; 141 (16): 3153-8.

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