Papers associated with primary germ layer (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.
	Expression of the adhesion G protein-coupled receptor A2 (adgra2) during Xenopus laevis development., Seigfried FA., Gene Expr Patterns. June 1, 2018; 28 54-61.
	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
	Inositol kinase and its product accelerate wound healing by modulating calcium levels, Rho GTPases, and F-actin assembly., Soto X., Proc Natl Acad Sci U S A. July 2, 2013; 110 (27): 11029-34.
	Gene switching at Xenopus laevis metamorphosis., Mukhi S., Dev Biol. February 15, 2010; 338 (2): 117-26.
	Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm., Carmona-Fontaine C., Dev Biol. September 15, 2007; 309 (2): 208-21.
	Xenopus fibrillin regulates directed convergence and extension., Skoglund P., Dev Biol. January 15, 2007; 301 (2): 404-16.
	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.
	A role for xGCNF in midbrain-hindbrain patterning in Xenopus laevis., Song K., Dev Biol. September 1, 1999; 213 (1): 170-9.
	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.
	Frzb, a secreted protein expressed in the Spemann organizer, binds and inhibits Wnt-8., Wang S., Cell. March 21, 1997; 88 (6): 757-66.
	Establishment of the dorso-ventral axis in Xenopus embryos is presaged by early asymmetries in beta-catenin that are modulated by the Wnt signaling pathway., Larabell CA., J Cell Biol. March 10, 1997; 136 (5): 1123-36.
	Overexpression of the homeobox gene Xnot-2 leads to notochord formation in Xenopus., Gont LK., Dev Biol. February 25, 1996; 174 (1): 174-8.
	Specification of the anteroposterior neural axis through synergistic interaction of the Wnt signaling cascade with noggin and follistatin., McGrew LL., Dev Biol. November 1, 1995; 172 (1): 337-42.
	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.
	Isolation and characterization of two forms of Xenopus prolactin., Yamashita K., Gen Comp Endocrinol. September 1, 1993; 91 (3): 307-17.
	Prolactin and interrenal hormone balance in adult specimens of Xenopus laevis exposed to hyperosmotic stress for up to one week., Guardabassi A., J Exp Zool. April 1, 1993; 265 (5): 515-21.
	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.
	Further study on the changes in the concentration of prolactin-binding sites in different organs of Xenopus laevis male and female, kept under dry conditions and then returned to water (their natural habitat)., Muccioli G., Gen Comp Endocrinol. June 1, 1989; 74 (3): 411-7.
	Prolactin binding sites in Xenopus laevis tissues: comparison between normal and dehydrated animals., Guardabassi A., Gen Comp Endocrinol. January 1, 1987; 65 (1): 40-7.

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