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

Papers associated with tail region (and prl.1)

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Mcrs1 interacts with Six1 to influence early craniofacial and otic development., Neilson KM., Dev Biol. November 1, 2020; 467 (1-2): 39-50.                  


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                                                             


Gene switching at Xenopus laevis metamorphosis., Mukhi S., Dev Biol. February 15, 2010; 338 (2): 117-26.                


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.


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.


Xenopus Cdc42 regulates convergent extension movements during gastrulation through Wnt/Ca2+ signaling pathway., Choi SC., Dev Biol. April 15, 2002; 244 (2): 342-57.                  


Overexpression of the Xenopus tight-junction protein claudin causes randomization of the left-right body axis., Brizuela BJ., Dev Biol. February 15, 2001; 230 (2): 217-29.                


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.


The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation., Kim SH., Development. December 1, 1998; 125 (23): 4681-90.                      


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.


Patterning of the neural ectoderm of Xenopus laevis by the amino-terminal product of hedgehog autoproteolytic cleavage., Lai CJ., Development. August 1, 1995; 121 (8): 2349-60.            


Zebrafish wnt8 and wnt8b share a common activity but are involved in distinct developmental pathways., Kelly GM., Development. June 1, 1995; 121 (6): 1787-99.  


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.


Gonadal hormones inhibit the induction of metamorphosis by thyroid hormones in Xenopus laevis tadpoles in vivo, but not in vitro., Gray KM., Gen Comp Endocrinol. February 1, 1990; 77 (2): 202-11.


Prolactin stabilizing action on the lysosomes in the tail and gut from Rana temporaria tadpoles at prometamorphosis., Giunta C., Gen Comp Endocrinol. June 1, 1972; 18 (3): 568-71.

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