Papers associated with posterior hypothalamus (and gal.2)

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	EBF factors drive expression of multiple classes of target genes governing neuronal development., Green YS., Neural Dev. April 30, 2011; 6 19.
	Gsx transcription factors repress Iroquois gene expression., Winterbottom EF., Dev Dyn. June 1, 2011; 240 (6): 1422-9.
	EBF proteins participate in transcriptional regulation of Xenopus muscle development., Green YS., Dev Biol. October 1, 2011; 358 (1): 240-50.
	The forkhead transcription factor FoxB1 regulates the dorsal-ventral and anterior-posterior patterning of the ectoderm during early Xenopus embryogenesis., Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.
	Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
	xCOUP-TF-B regulates xCyp26 transcription and modulates retinoic acid signaling for anterior neural patterning in Xenopus., Tanibe M., Int J Dev Biol. January 1, 2012; 56 (4): 239-44.
	Geminin is required for zygotic gene expression at the Xenopus mid-blastula transition., Kerns SL., PLoS One. January 1, 2012; 7 (5): e38009.
	mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells., Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
	Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	The RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus., Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.
	A hindbrain-repressive Wnt3a/Meis3/Tsh1 circuit promotes neuronal differentiation and coordinates tissue maturation., Elkouby YM., Development. April 1, 2012; 139 (8): 1487-97.
	Exons 5-15 of kazrin are dispensable for murine epidermal morphogenesis and homeostasis., Chhatriwala MK., J Invest Dermatol. August 1, 2012; 132 (8): 1977-87.
	Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development., Xu Y, Xu Y., Cell. December 7, 2012; 151 (6): 1200-13.
	Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Mutually exclusive signaling signatures define the hepatic and pancreatic progenitor cell lineage divergence., Rodríguez-Seguel E., Genes Dev. September 1, 2013; 27 (17): 1932-46.
	RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.
	Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling., Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.
	NumbL is essential for Xenopus primary neurogenesis., Nieber F., BMC Dev Biol. October 14, 2013; 13 36.
	Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein., Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
	PV.1 suppresses the expression of FoxD5b during neural induction in Xenopus embryos., Yoon J., Mol Cells. March 1, 2014; 37 (3): 220-5.
	A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis., Dubaissi E., Development. April 1, 2014; 141 (7): 1514-25.
	RFX7 is required for the formation of cilia in the neural tube., Manojlovic Z., Mech Dev. May 1, 2014; 132 28-37.

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