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Summary Anatomy Item Literature (2349) Expression Attributions Wiki
XB-ANAT-4083

Papers associated with tadpole (and wnt5a)

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Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax., Wang S., Cell Biosci. February 23, 2023; 13 (1): 40.              

Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH., Dev Biol. March 1, 2022; 483 157-168.                  

Xenopus laevis il11ra.L is an experimentally proven interleukin-11 receptor component that is required for tadpole tail regeneration., Suzuki S., Sci Rep. February 3, 2022; 12 (1): 1903.                      

Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs., Aztekin C., Development. June 1, 2021; 148 (11):                                             

Thyroid Hormone Receptor Is Essential for Larval Epithelial Apoptosis and Adult Epithelial Stem Cell Development but Not Adult Intestinal Morphogenesis during Xenopus tropicalis Metamorphosis., Shibata Y., Cells. March 3, 2021; 10 (3):                             

The Secreted Protein Disulfide Isomerase Ag1 Lost by Ancestors of Poorly Regenerating Vertebrates Is Required for Xenopus laevis Tail Regeneration., Ivanova AS., Front Cell Dev Biol. January 1, 2021; 9 738940.                  

Thyroid hormone-induced expression of Foxl1 in subepithelial fibroblasts correlates with adult stem cell development during Xenopus intestinal remodeling., Hasebe T., Sci Rep. November 26, 2020; 10 (1): 20715.                

Xvent-2 expression in regenerating Xenopus tails., Pshennikova ES., Stem Cell Investig. July 20, 2020; 7 13.  

Thyroid hormone receptor beta is critical for intestinal remodeling during Xenopus tropicalis metamorphosis., Shibata Y., Cell Biosci. March 27, 2020; 10 46.                            

Bioinformatics Screening of Genes Specific for Well-Regenerating Vertebrates Reveals c-answer, a Regulator of Brain Development and Regeneration., Korotkova DD., Cell Rep. October 22, 2019; 29 (4): 1027-1040.e6.                              

Cholesterol-rich membrane microdomains modulate Wnt/β-catenin morphogen gradient during Xenopus development., Reis AH., Mech Dev. November 1, 2016; 142 30-39.                        

Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  

Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.                            

Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling., Sheng R., Nat Commun. July 15, 2014; 5 4393.              

Thyroid hormone-regulated Wnt5a/Ror2 signaling is essential for dedifferentiation of larval epithelial cells into adult stem cells in the Xenopus laevis intestine., Ishizuya-Oka A., PLoS One. January 1, 2014; 9 (9): e107611.                            

Mutually exclusive signaling signatures define the hepatic and pancreatic progenitor cell lineage divergence., Rodríguez-Seguel E., Genes Dev. September 1, 2013; 27 (17): 1932-46.    

Imparting regenerative capacity to limbs by progenitor cell transplantation., Lin G., Dev Cell. January 14, 2013; 24 (1): 41-51.                          

Rspo3 binds syndecan 4 and induces Wnt/PCP signaling via clathrin-mediated endocytosis to promote morphogenesis., Ohkawara B., Dev Cell. March 15, 2011; 20 (3): 303-14.                        

Wnt5a/Ror2-induced upregulation of xPAPC requires xShcA., Feike AC., Biochem Biophys Res Commun. October 1, 2010; 400 (4): 500-6.              

XsFRP5 modulates endodermal organogenesis in Xenopus laevis., Damianitsch K., Dev Biol. May 15, 2009; 329 (2): 327-37.      

Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis., Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.                                

Xenopus Wnt-5a induces an ectopic larval tail at injured site, suggesting a crucial role for noncanonical Wnt signal in tail regeneration., Sugiura T., Mech Dev. January 1, 2009; 126 (1-2): 56-67.    

Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.              

Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK., Cell Commun Signal. October 19, 2005; 3 12.          

Regulation of Msx genes by a Bmp gradient is essential for neural crest specification., Tribulo C., Development. December 1, 2003; 130 (26): 6441-52.            

Mutual antagonism between dickkopf1 and dickkopf2 regulates Wnt/beta-catenin signalling., Wu W., Curr Biol. December 1, 2000; 10 (24): 1611-4.        

The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.              

Evolutionary relationships between the amphibian, avian, and mammalian stomachs., Smith DM., Evol Dev. January 1, 2000; 2 (6): 348-59.

Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.                  

Xwnt-5A: a maternal Wnt that affects morphogenetic movements after overexpression in embryos of Xenopus laevis., Moon RT., Development. September 1, 1993; 119 (1): 97-111.                  

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