Papers associated with primary germ layer (and mlc1)

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	Ectoderm to mesoderm transition by down-regulation of actomyosin contractility., Kashkooli L., PLoS Biol. January 6, 2021; 19 (1): e3001060.
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.
	Variable combinations of specific ephrin ligand/Eph receptor pairs control embryonic tissue separation., Rohani N., PLoS Biol. September 23, 2014; 12 (9): e1001955.
	GEF-H1 functions in apical constriction and cell intercalations and is essential for vertebrate neural tube closure., Itoh K., J Cell Sci. June 1, 2014; 127 (Pt 11): 2542-53.
	The Xenopus homologue of Down syndrome critical region protein 6 drives dorsoanterior gene expression and embryonic axis formation by antagonising polycomb group proteins., Li HY., Development. December 1, 2013; 140 (24): 4903-13.
	The tumor-associated EpCAM regulates morphogenetic movements through intracellular signaling., Maghzal N., J Cell Biol. November 1, 2010; 191 (3): 645-59.
	The involvement of lethal giant larvae and Wnt signaling in bottle cell formation in Xenopus embryos., Choi SC., Dev Biol. December 1, 2009; 336 (1): 68-75.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
	Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
	Redundancy and evolution of GATA factor requirements in development of the myocardium., Peterkin T., Dev Biol. November 15, 2007; 311 (2): 623-35.
	Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development., Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
	The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart., Smith SJ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.
	Connective-tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex., Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.
	Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants., Latinkić BV., Development. August 1, 2003; 130 (16): 3865-76.
	Xenopus bagpipe-related gene, koza, may play a role in regulation of cell proliferation., Newman CS., Dev Dyn. December 1, 2002; 225 (4): 571-80.
	An anterior signalling centre in Xenopus revealed by the homeobox gene XHex., Jones CM., Curr Biol. September 9, 1999; 9 (17): 946-54.
	In vitro cytotoxicity in adult Xenopus generated against larval targets and minor histocompatibility antigens., Horton TL., Transplantation. May 1, 1989; 47 (5): 880-2.
	Impaired rejection of minor-histocompatibility-antigen-disparate skin grafts and acquisition of tolerance to thymus donor antigens in allothymus-implanted, thymectomized Xenopus., Arnall JC., Transplantation. June 1, 1986; 41 (6): 766-76.
	Induction of T cell differentiation in early-thymectomized Xenopus by grafting adult thymuses from either MHC-matched or from partially or totally MHC-mismatched donors., Nagata S., Thymus. January 1, 1984; 6 (1-2): 89-103.

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