Papers associated with olfactory system (and chrd)

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	Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling., Watanabe T., Genesis. October 1, 2014; .
	Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus., Colozza G., Differentiation. July 1, 2014; 88 (1): 17-26.
	FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.
	Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.
	Regulation of early xenopus embryogenesis by Smad ubiquitination regulatory factor 2., Das S., Dev Dyn. August 1, 2012; 241 (8): 1260-73.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.
	Xenopus Teashirt1 regulates posterior identity in brain and cranial neural crest., Koebernick K., Dev Biol. October 1, 2006; 298 (1): 312-26.
	The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
	An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.
	Tsukushi functions as an organizer inducer by inhibition of BMP activity in cooperation with chordin., Ohta K., Dev Cell. September 1, 2004; 7 (3): 347-358.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	A novel chordin-like protein inhibitor for bone morphogenetic proteins expressed preferentially in mesenchymal cell lineages., Nakayama N., Dev Biol. April 15, 2001; 232 (2): 372-87.
	Wnt antagonism initiates cardiogenesis in Xenopus laevis., Schneider VA., Genes Dev. February 1, 2001; 15 (3): 304-15.
	A direct screen for secreted proteins in Xenopus embryos identifies distinct activities for the Wnt antagonists Crescent and Frzb-1., Pera EM., Mech Dev. September 1, 2000; 96 (2): 183-95.
	Xenopus GDF6, a new antagonist of noggin and a partner of BMPs., Chang C., Development. August 1, 1999; 126 (15): 3347-57.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.

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