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Summary Anatomy Item Literature (2148) Expression Attributions Wiki
XB-ANAT-1602

Papers associated with regenerating tail (and pax2)

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Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.                      


Rdh10a Provides a Conserved Critical Step in the Synthesis of Retinoic Acid during Zebrafish Embryogenesis., D'Aniello E., PLoS One. September 1, 2015; 10 (9): e0138588.                  


Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.                        


Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney., Sauert K., PLoS One. January 1, 2012; 7 (3): e33522.                  


Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.                        


PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B., BMC Dev Biol. June 10, 2011; 11 36.                          


Retinoic acid is a key regulatory switch determining the difference between lung and thyroid fates in Xenopus laevis., Wang JH., BMC Dev Biol. January 26, 2011; 11 75.                            


In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      


Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          


Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.                                


Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development., Fujimi TJ., Gene Expr Patterns. July 1, 2008; 8 (6): 376-381.                          


Cadherin-6 is required for zebrafish nephrogenesis during early development., Kubota F., Int J Dev Biol. January 1, 2007; 51 (2): 123-9.


Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.                  


Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.                          


Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.                


Conserved expression control and shared activity between cognate T-box genes Tbx2 and Tbx3 in connection with Sonic hedgehog signaling during Xenopus eye development., Takabatake Y., Dev Growth Differ. August 1, 2002; 44 (4): 257-71.              


A role for Xlim-1 in pronephros development in Xenopus laevis., Chan TC., Dev Biol. December 15, 2000; 228 (2): 256-69.      


Notch regulates cell fate in the developing pronephros., McLaughlin KA., Dev Biol. November 15, 2000; 227 (2): 567-80.            


Evidence for non-axial A/P patterning in the nonneural ectoderm of Xenopus and zebrafish pregastrula embryos., Read EM., Int J Dev Biol. September 1, 1998; 42 (6): 763-74.    

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