Papers associated with cranium (and foxg1)

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	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	Isoquercitrin suppresses colon cancer cell growth in vitro by targeting the Wnt/β-catenin signaling pathway., Amado NG., J Biol Chem. December 19, 2014; 289 (51): 35456-67.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation., Juraver-Geslin HA., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.
	Integration of telencephalic Wnt and hedgehog signaling center activities by Foxg1., Danesin C., Dev Cell. April 1, 2009; 16 (4): 576-87.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	Regulation of vertebrate eye development by Rx genes., Bailey TJ., Int J Dev Biol. January 1, 2004; 48 (8-9): 761-70.
	FGF signaling and the anterior neural induction in Xenopus., Hongo I., Dev Biol. December 15, 1999; 216 (2): 561-81.

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