Papers associated with primary germ layer (and ighx)

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	Roles of two types of heparan sulfate clusters in Wnt distribution and signaling in Xenopus., Mii Y., Nat Commun. December 7, 2017; 8 (1): 1973.
	Ouro proteins are not essential to tail regression during Xenopus tropicalis metamorphosis., Nakai Y., Genes Cells. March 1, 2016; 21 (3): 275-86.
	Immunomodulation in post-metamorphic northern leopard frogs, Lithobates pipiens, following larval exposure to polybrominated diphenyl ether., Cary TL., Environ Sci Technol. May 20, 2014; 48 (10): 5910-9.
	Generation of monoclonal antibodies against the Galβ1-4Gal epitope: a key tool in studies of species-specific glycans expressed in fish, amphibians and birds., Suzuki N., Glycobiology. January 1, 2013; 23 (1): 91-105.
	Immune defenses against Batrachochytrium dendrobatidis, a fungus linked to global amphibian declines, in the South African clawed frog, Xenopus laevis., Ramsey JP., Infect Immun. September 1, 2010; 78 (9): 3981-92.
	Larval antigen molecules recognized by adult immune cells of inbred Xenopus laevis: partial characterization and implication in metamorphosis., Izutsu Y., Dev Growth Differ. December 1, 2002; 44 (6): 477-88.
	Possible role of the 38 kDa protein, lacking in the gastrula-arrested Xenopus mutant, in gastrulation., Tanaka TS., Dev Growth Differ. February 1, 2002; 44 (1): 23-33.
	Skin xenograft rejection in Xenopus--immunohistology and effect of thymectomy., Horton JD., Transplantation. February 1, 1992; 53 (2): 473-6.
	Immune responses of thymus/lymphocyte embryonic chimeras: studies on tolerance and major histocompatibility complex restriction in Xenopus., Flajnik MF., Eur J Immunol. June 1, 1985; 15 (6): 540-7.

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