Papers associated with posterior cardinal vein

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	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.
	VEGF mediates angioblast migration during development of the dorsal aorta in Xenopus., Cleaver O., Development. October 1, 1998; 125 (19): 3905-14.
	Towards a molecular anatomy of the Xenopus pronephric kidney., Brändli AW., Int J Dev Biol. January 1, 1999; 43 (5): 381-95.
	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.
	Comparative analysis of embryonic gene expression defines potential interaction sites for Xenopus EphB4 receptors with ephrin-B ligands., Helbling PM., Dev Dyn. December 1, 1999; 216 (4-5): 361-73.
	The receptor tyrosine kinase EphB4 and ephrin-B ligands restrict angiogenic growth of embryonic veins in Xenopus laevis., Helbling PM., Development. January 1, 2000; 127 (2): 269-78.
	Distinct origins of adult and embryonic blood in Xenopus., Ciau-Uitz A., Cell. September 15, 2000; 102 (6): 787-96.
	Distinct enhancer elements control Hex expression during gastrulation and early organogenesis., Rodriguez TA., Dev Biol. June 15, 2001; 234 (2): 304-16.
	Endoderm is required for vascular endothelial tube formation, but not for angioblast specification., Vokes SA., Development. February 1, 2002; 129 (3): 775-85.
	Degradation of hyaluronan by a Hyal2-type hyaluronidase affects pattern formation of vitelline vessels during embryogenesis of Xenopus laevis., Müllegger J., Mech Dev. February 1, 2002; 111 (1-2): 25-35.
	Cloning and developmental expression of Baf57 in Xenopus laevis., Domingos PM., Mech Dev. August 1, 2002; 116 (1-2): 177-81.
	Fluorescent labeling of endothelial cells allows in vivo, continuous characterization of the vascular development of Xenopus laevis., Levine AJ., Dev Biol. February 1, 2003; 254 (1): 50-67.
	Xenopus Cyr61 regulates gastrulation movements and modulates Wnt signalling., Latinkic BV., Development. June 1, 2003; 130 (11): 2429-41.
	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.
	Comparative genomic and expression analysis of the conserved NTPDase gene family in Xenopus., Massé K., Genomics. March 1, 2006; 87 (3): 366-81.
	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.
	A novel gene, Ami is expressed in vascular tissue in Xenopus laevis., Inui M., Gene Expr Patterns. August 1, 2006; 6 (6): 613-9.
	Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.
	Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
	Paracrine and autocrine mechanisms of apelin signaling govern embryonic and tumor angiogenesis., Kälin RE., Dev Biol. May 15, 2007; 305 (2): 599-614.
	A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
	A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development., Rodrigues CO., Development. June 1, 2008; 135 (11): 1903-11.
	A functional screen for genes involved in Xenopus pronephros development., Kyuno J., Mech Dev. July 1, 2008; 125 (7): 571-86.
	XRASGRP2 expression during early development of Xenopus embryos., Nagamine K., Biochem Biophys Res Commun. August 8, 2008; 372 (4): 886-91.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis., Koestner U., Dev Dyn. December 1, 2008; 237 (12): 3853-63.
	Combinatorial regulation of endothelial gene expression by ets and forkhead transcription factors., De Val S., Cell. December 12, 2008; 135 (6): 1053-64.
	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.
	FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy., Wuebbles RD., Dis Model Mech. January 1, 2009; 2 (5-6): 267-74.
	Kruppel-like factor 2 cooperates with the ETS family protein ERG to activate Flk1 expression during vascular development., Meadows SM., Development. April 1, 2009; 136 (7): 1115-25.
	Rasip1 is required for endothelial cell motility, angiogenesis and vessel formation., Xu K., Dev Biol. May 15, 2009; 329 (2): 269-79.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Ectophosphodiesterase/nucleotide phosphohydrolase (Enpp) nucleotidases: cloning, conservation and developmental restriction., Massé K., Int J Dev Biol. January 1, 2010; 54 (1): 181-93.
	XRASGRP2 is essential for blood vessel formation during Xenopus development., Suzuki K., Int J Dev Biol. January 1, 2010; 54 (4): 609-15.
	ETS family protein ETV2 is required for initiation of the endothelial lineage but not the hematopoietic lineage in the Xenopus embryo., Salanga MC., Dev Dyn. April 1, 2010; 239 (4): 1178-87.
	Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9.
	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.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	Role of synectin in lymphatic development in zebrafish and frogs., Hermans K., Blood. October 28, 2010; 116 (17): 3356-66.
	Xenopus er71 is involved in vascular development., Neuhaus H., Dev Dyn. December 1, 2010; 239 (12): 3436-45.
	The transcriptional coactivators Yap and TAZ are expressed during early Xenopus development., Nejigane S., Int J Dev Biol. January 1, 2011; 55 (1): 121-6.
	EBF factors drive expression of multiple classes of target genes governing neuronal development., Green YS., Neural Dev. April 30, 2011; 6 19.
	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.
	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.
	Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration., Love NR., BMC Dev Biol. November 15, 2011; 11 70.
	Expression analysis of the peroxiredoxin gene family during early development in Xenopus laevis., Shafer ME., Gene Expr Patterns. December 1, 2011; 11 (8): 511-6.
	Activity-based labeling of matrix metalloproteinases in living vertebrate embryos., Keow JY., PLoS One. January 1, 2012; 7 (8): e43434.
	Evolutionarily repurposed networks reveal the well-known antifungal drug thiabendazole to be a novel vascular disrupting agent., Cha HJ., PLoS Biol. January 1, 2012; 10 (8): e1001379.
	Maturation of the gastric microvasculature in Xenopus laevis (Lissamphibia, Anura) occurs at the transition from the herbivorous to the carnivorous lifestyle, predominantly by intussuceptive microvascular growth (IMG): a scanning electron microscope study of microvascular corrosion casts and correlative light microscopy., Lametschwandtner A., Anat Sci Int. June 1, 2012; 87 (2): 88-100.

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