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Summary Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-86

Papers associated with tail region (and prl.2)

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Dual control of pcdh8l/PCNS expression and function in Xenopus laevis neural crest cells by adam13/33 via the transcription factors tfap2α and arid3a., Khedgikar V., Elife. August 22, 2017; 6                                                             


Multiple functions of FADD in apoptosis, NF-κB-related signaling, and heart development in Xenopus embryos., Sakamaki K., Genes Cells. November 1, 2012; 17 (11): 875-96.                                  


Comparative expression analysis of the H3K27 demethylases, JMJD3 and UTX, with the H3K27 methylase, EZH2, in Xenopus., Kawaguchi A., Int J Dev Biol. January 1, 2012; 56 (4): 295-300.                                          


Xenopus Dbx2 is involved in primary neurogenesis and early neural plate patterning., Ma P., Biochem Biophys Res Commun. August 19, 2011; 412 (1): 170-4.            


A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA., Dev Biol. March 15, 2011; 351 (2): 297-310.                            


Corticosteroids disrupt amphibian metamorphosis by complex modes of action including increased prolactin expression., Lorenz C., Comp Biochem Physiol C Toxicol Pharmacol. August 1, 2009; 150 (2): 314-21.


HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.                        


One of the duplicated matrix metalloproteinase-9 genes is expressed in regressing tail during anuran metamorphosis., Fujimoto K., Dev Growth Differ. May 1, 2006; 48 (4): 223-41.            


Temporal and spatial expression patterns of FoxN genes in Xenopus laevis embryos., Schuff M., Int J Dev Biol. January 1, 2006; 50 (4): 429-34.      


Tissue-specific regulation of type III iodothyronine 5-deiodinase gene expression mediates the effects of prolactin and growth hormone in Xenopus metamorphosis., Shintani N., Dev Growth Differ. August 1, 2002; 44 (4): 327-35.


Expression and function of Xenopus laevis p75(NTR) suggest evolution of developmental regulatory mechanisms., Hutson LD., J Neurobiol. November 5, 2001; 49 (2): 79-98.                      


Xebf3 is a regulator of neuronal differentiation during primary neurogenesis in Xenopus., Pozzoli O., Dev Biol. May 15, 2001; 233 (2): 495-512.            


Xenopus frizzled-5: a frizzled family member expressed exclusively in the neural retina of the developing eye., Sumanas S., Mech Dev. May 1, 2001; 103 (1-2): 133-6.  


Cloning of a cDNA for Xenopus prolactin receptor and its metamorphic expression profile., Yamamoto T., Dev Growth Differ. April 1, 2000; 42 (2): 167-74.          


Prolactin is not a juvenile hormone in Xenopus laevis metamorphosis., Huang H., Proc Natl Acad Sci U S A. January 4, 2000; 97 (1): 195-9.


Contrasting patterns of expression of thyroid hormone and retinoid X receptor genes during hormonal manipulation of Xenopus tadpole tail regression in culture., Iwamuro S., Mol Cell Endocrinol. September 22, 1995; 113 (2): 235-43.


Hormonal regulation of programmed cell death during amphibian metamorphosis., Tata JR., Biochem Cell Biol. January 1, 1994; 72 (11-12): 581-8.


Isolation and characterization of two forms of Xenopus prolactin., Yamashita K., Gen Comp Endocrinol. September 1, 1993; 91 (3): 307-17.


Prolactin inhibits both thyroid hormone-induced morphogenesis and cell death in cultured amphibian larval tissues., Tata JR., Dev Biol. July 1, 1991; 146 (1): 72-80.

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