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Summary Anatomy Item Literature (813) Expression Attributions Wiki
XB-ANAT-448

Papers associated with circulatory system (and odc1)

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maea affects head formation through ß-catenin degradation during early Xenopus laevis development., Goto T., Dev Growth Differ. January 1, 2023; 65 (1): 29-36.                  


The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus., Melchert J., Dev Biol. March 15, 2020; 459 (2): 138-148.                                


Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.                                    


Xenopus embryonic epidermis as a mucociliary cellular ecosystem to assess the effect of sex hormones in a non-reproductive context., Castillo-Briceno P., Front Zool. February 6, 2014; 11 (1): 9.                


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.            


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.            


zfp36 expression delineates both myeloid cells and cells localized to the fusing neural folds in Xenopus tropicalis., Noiret M., Int J Dev Biol. January 1, 2014; 58 (10-12): 751-5.                


Myb promotes centriole amplification and later steps of the multiciliogenesis program., Tan FE., Development. October 1, 2013; 140 (20): 4277-86.                


ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3., Hoff S., Nat Genet. August 1, 2013; 45 (8): 951-6.                                


β-Adrenergic signaling promotes posteriorization in Xenopus early development., Mori S., Dev Growth Differ. April 1, 2013; 55 (3): 350-8.            


Uncoupling VEGFA functions in arteriogenesis and hematopoietic stem cell specification., Leung A., Dev Cell. January 28, 2013; 24 (2): 144-58.                                


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.                      


Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart., Puskaric S., Hum Mol Genet. December 1, 2010; 19 (23): 4625-33.            


Tel1/ETV6 specifies blood stem cells through the agency of VEGF signaling., Ciau-Uitz A., Dev Cell. April 20, 2010; 18 (4): 569-78.                


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


Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.                  


Amphibian in vitro heart induction: a simple and reliable model for the study of vertebrate cardiac development., Ariizumi T., Int J Dev Biol. September 1, 2003; 47 (6): 405-10.      


Isolation and characterization of three novel serine protease genes from Xenopus laevis., Yamada K., Gene. July 11, 2000; 252 (1-2): 209-16.        


FOG acts as a repressor of red blood cell development in Xenopus., Deconinck AE., Development. May 1, 2000; 127 (10): 2031-40.              


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.      

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