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Summary Anatomy Item Literature (2231) Expression Attributions Wiki
XB-ANAT-3282

Papers associated with posterior hypothalamus (and aplnr)

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VEGF mediates angioblast migration during development of the dorsal aorta in Xenopus., Cleaver O., Development. October 1, 1998; 125 (19): 3905-14.          


Endoderm is required for vascular endothelial tube formation, but not for angioblast specification., Vokes SA., Development. February 1, 2002; 129 (3): 775-85.            


Embryonic expression of Xenopus laevis SOX7., Fawcett SR., Gene Expr Patterns. January 1, 2004; 4 (1): 29-33.          


Genomic analysis of Xenopus organizer function., Hufton AL., BMC Dev Biol. June 6, 2006; 6 27.                  


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.                  


Cloning and activation of the bullfrog apelin receptor: Gi/o coupling and high affinity for [Pro1]apelin-13., Moon MJ., Mol Cell Endocrinol. October 15, 2007; 277 (1-2): 51-60.


A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.                  


The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development., Kazanskaya O., Development. November 1, 2008; 135 (22): 3655-64.                


A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds., Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.                


Rasip1 is required for endothelial cell motility, angiogenesis and vessel formation., Xu K., Dev Biol. May 15, 2009; 329 (2): 269-79.      


Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.          


Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.                


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


Notch signaling, wt1 and foxc2 are key regulators of the podocyte gene regulatory network in Xenopus., White JT., Development. June 1, 2010; 137 (11): 1863-73.                            


Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.                          


Hippo signaling components, Mst1 and Mst2, act as a switch between self-renewal and differentiation in Xenopus hematopoietic and endothelial progenitors., Nejigane S., Int J Dev Biol. January 1, 2013; 57 (5): 407-14.                      


Regulation of primitive hematopoiesis by class I histone deacetylases., Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.              


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.        


Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4., Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.            

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