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Summary Anatomy Item Literature (33) Expression Attributions Wiki
XB-ANAT-1641

Papers associated with vitelline vein

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The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly., Smith SJ., Dev Biol. August 15, 2016; 416 (2): 373-88.                                                      


Suppression of vascular network formation by chronic hypoxia and prolyl-hydroxylase 2 (phd2) deficiency during vertebrate development., Metikala S., Angiogenesis. April 1, 2016; 19 (2): 119-31.  


Expression and localization of Rdd proteins in Xenopus embryo., Lim JC., Anat Cell Biol. March 1, 2014; 47 (1): 18-27.          


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.            


CASZ1 promotes vascular assembly and morphogenesis through the direct regulation of an EGFL7/RhoA-mediated pathway., Charpentier MS., Dev Cell. April 29, 2013; 25 (2): 132-43.        


sox4 and sox11 function during Xenopus laevis eye development., Cizelsky W., PLoS One. January 1, 2013; 8 (7): e69372.              


Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos., Canning CA., Dev Dyn. August 1, 2011; 240 (8): 1958-63.                                                  


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.                      


Xenopus er71 is involved in vascular development., Neuhaus H., Dev Dyn. December 1, 2010; 239 (12): 3436-45.            


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.                                                


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.                                    


XRASGRP2 is essential for blood vessel formation during Xenopus development., Suzuki K., Int J Dev Biol. January 1, 2010; 54 (4): 609-15.            


FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy., Wuebbles RD., Dis Model Mech. May 1, 2009; 2 (5-6): 267-74.                  


Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.              


spib is required for primitive myeloid development in Xenopus., Costa RM., Blood. September 15, 2008; 112 (6): 2287-96.                                      


XRASGRP2 expression during early development of Xenopus embryos., Nagamine K., Biochem Biophys Res Commun. August 8, 2008; 372 (4): 886-91.        


A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development., Rodrigues CO., Development. June 1, 2008; 135 (11): 1903-11.              


HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.                        


Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.                                


Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.                


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.        


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.                      


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.          


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.    


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.              


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 origins of primitive blood in Xenopus: implications for axial patterning., Lane MC., Development. February 1, 1999; 126 (3): 423-34.            


Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins., Sparrow DB., Mech Dev. February 1, 1998; 71 (1-2): 151-63.            


Neovascularization of the Xenopus embryo., Cleaver O., Dev Dyn. September 1, 1997; 210 (1): 66-77.        


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.        


Intraembryonic origin of hepatic hematopoiesis in Xenopus laevis., Chen XD., J Immunol. March 15, 1995; 154 (6): 2557-67.


A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus., Dent JA., Development. January 1, 1989; 105 (1): 61-74.                      

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