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Summary Anatomy Item Literature (48) Expression Attributions Wiki
XB-ANAT-81

Papers associated with circumblastoporal collar (and tbxt)

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RARγ is required for mesodermal gene expression prior to gastrulation in Xenopus., Janesick A., Development. September 17, 2018; 145 (18):                           


Intracellular calcium signal at the leading edge regulates mesodermal sheet migration during Xenopus gastrulation., Hayashi K., Sci Rep. February 5, 2018; 8 (1): 2433.              


Identification of p62/SQSTM1 as a component of non-canonical Wnt VANGL2-JNK signalling in breast cancer., Puvirajesinghe TM., Nat Commun. January 12, 2016; 7 10318.                                  


The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS., Cell Rep. February 3, 2015; 10 (4): 527-36.                    


Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.                      


Competition for ligands between FGFR1 and FGFR4 regulates Xenopus neural development., Yamagishi M., Int J Dev Biol. January 1, 2010; 54 (1): 93-104.          


Gastrulation of Gastrotheca riobambae in comparison with other frogs., Moya IM., Dev Biol. April 15, 2007; 304 (2): 467-78.


ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.                


Function of the two Xenopus smad4s in early frog development., Chang C., J Biol Chem. October 13, 2006; 281 (41): 30794-803.                


Heading in a new direction: implications of the revised fate map for understanding Xenopus laevis development., Lane MC., Dev Biol. August 1, 2006; 296 (1): 12-28.                


Interaction between X-Delta-2 and Hox genes regulates segmentation and patterning of the anteroposterior axis., Peres JN., Mech Dev. April 1, 2006; 123 (4): 321-33.                          


The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.                              


Timed interactions between the Hox expressing non-organiser mesoderm and the Spemann organiser generate positional information during vertebrate gastrulation., Wacker SA., Dev Biol. April 1, 2004; 268 (1): 207-19.            


The initiation of Hox gene expression in Xenopus laevis is controlled by Brachyury and BMP-4., Wacker SA., Dev Biol. February 1, 2004; 266 (1): 123-37.                  


The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW., Dev Biol. October 15, 2001; 238 (2): 303-14.              


XCL-2 is a novel m-type calpain and disrupts morphogenetic movements during embryogenesis in Xenopus laevis., Cao Y., Dev Growth Differ. October 1, 2001; 43 (5): 563-71.              


Making mesoderm--upstream and downstream of Xbra., Smith JC., Int J Dev Biol. January 1, 2001; 45 (1): 219-24.    


Gli2 functions in FGF signaling during antero-posterior patterning., Brewster R., Development. October 1, 2000; 127 (20): 4395-405.            


Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth., Beck CW., Mech Dev. March 1, 1998; 72 (1-2): 41-52.                                                                


The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos., Zorn AM., Genes Dev. September 1, 1997; 11 (17): 2176-90.                  


Tail formation as a continuation of gastrulation: the multiple cell populations of the Xenopus tailbud derive from the late blastopore lip., Gont LK., Development. December 1, 1993; 119 (4): 991-1004.                

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