Papers associated with cement gland (and hba1)

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	Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.
	Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.
	Xenopus nucleosome assembly protein becomes tissue-restricted during development and can alter the expression of specific genes., Steer WM., Mech Dev. September 1, 2003; 120 (9): 1045-57.
	Common and distinct signals specify the distribution of blood and vascular cell lineages in Xenopus laevis embryos., Iraha F., Dev Growth Differ. October 1, 2002; 44 (5): 395-407.
	Endoderm specification and differentiation in Xenopus embryos., Horb ME., Dev Biol. August 15, 2001; 236 (2): 330-43.
	Use of large-scale expression cloning screens in the Xenopus laevis tadpole to identify gene function., Grammer TC., Dev Biol. December 15, 2000; 228 (2): 197-210.
	OAZ uses distinct DNA- and protein-binding zinc fingers in separate BMP-Smad and Olf signaling pathways., Hata A., Cell. January 21, 2000; 100 (2): 229-40.
	A truncated bone morphogenetic protein 4 receptor alters the fate of ventral mesoderm to dorsal mesoderm: roles of animal pole tissue in the development of ventral mesoderm., Maéno M., Proc Natl Acad Sci U S A. October 25, 1994; 91 (22): 10260-4.
	Localization of specific mRNAs in Xenopus embryos by whole-mount in situ hybridization., Hemmati-Brivanlou A., Development. October 1, 1990; 110 (2): 325-30.

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