Papers associated with tail (and prl.2)

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	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.
	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.
	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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