Papers associated with spinal cord (and nrp1)

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	Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development., Yan B., Dev Dyn. February 1, 2015; 244 (2): 181-210.
	Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates., Yajima H., BMC Biol. May 29, 2014; 12 40.
	Nkx6 genes pattern the frog neural plate and Nkx6.1 is necessary for motoneuron axon projection., Dichmann DS., Dev Biol. January 15, 2011; 349 (2): 378-86.
	Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.
	BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus., Wills AE., Dev Biol. January 15, 2010; 337 (2): 335-50.
	Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function., Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.
	Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis., Koestner U., Dev Dyn. December 1, 2008; 237 (12): 3853-63.
	Vertebrate Ctr1 coordinates morphogenesis and progenitor cell fate and regulates embryonic stem cell differentiation., Haremaki T., Proc Natl Acad Sci U S A. July 17, 2007; 104 (29): 12029-34.
	Role of X-Delta-2 in the early neural development of Xenopus laevis., Peres JN., Dev Dyn. March 1, 2006; 235 (3): 802-10.
	Cooperative non-cell and cell autonomous regulation of Nodal gene expression and signaling by Lefty/Antivin and Brachyury in Xenopus., Cha YR., Dev Biol. February 15, 2006; 290 (2): 246-64.
	Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis., Shibata M., Mech Dev. December 1, 2005; 122 (12): 1322-39.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation., Hartley KO., Dev Biol. October 1, 2001; 238 (1): 168-84.
	XMeis3 protein activity is required for proper hindbrain patterning in Xenopus laevis embryos., Dibner C., Development. September 1, 2001; 128 (18): 3415-26.
	The Alzheimer-related gene presenilin-1 facilitates sonic hedgehog expression in Xenopus primary neurogenesis., Paganelli AR., Mech Dev. September 1, 2001; 107 (1-2): 119-31.
	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.
	Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis., Ribisi S., Dev Biol. November 1, 2000; 227 (1): 183-96.
	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.
	Functional association of retinoic acid and hedgehog signaling in Xenopus primary neurogenesis., Franco PG., Development. October 1, 1999; 126 (19): 4257-65.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	A Meis family protein caudalizes neural cell fates in Xenopus., Salzberg A., Mech Dev. January 1, 1999; 80 (1): 3-13.
	XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.
	Patterning of the neural ectoderm of Xenopus laevis by the amino-terminal product of hedgehog autoproteolytic cleavage., Lai CJ., Development. August 1, 1995; 121 (8): 2349-60.
	Dorsal-ventral patterning and differentiation of noggin-induced neural tissue in the absence of mesoderm., Knecht AK., Development. June 1, 1995; 121 (6): 1927-35.
	An aberrant retinal pathway and visual centers in Xenopus tadpoles share a common cell surface molecule, A5 antigen., Fujisawa H., Dev Biol. October 1, 1989; 135 (2): 231-40.

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