Papers associated with hindbrain (and acta4)

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	T-type Calcium Channel Regulation of Neural Tube Closure and EphrinA/EPHA Expression., Abdul-Wajid S., Cell Rep. October 27, 2015; 13 (4): 829-839.
	Characterization of the hypothalamus of Xenopus laevis during development. II. The basal regions., Domínguez L., J Comp Neurol. April 1, 2014; 522 (5): 1102-31.
	A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle., Sartelet A., Dis Model Mech. January 1, 2014; 7 (1): 119-28.
	Calponin 2 acts as an effector of noncanonical Wnt-mediated cell polarization during neural crest cell migration., Ulmer B., Cell Rep. March 28, 2013; 3 (3): 615-21.
	The Anolis lizard genome: an amniote genome without isochores., Fujita MK., Genome Biol Evol. January 1, 2011; 3 974-84.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Developmental expression of retinoic acid receptors (RARs)., Dollé P., Nucl Recept Signal. May 12, 2009; 7 e006.
	Neuronal leucine-rich repeat 6 (XlNLRR-6) is required for late lens and retina development in Xenopus laevis., Wolfe AD., Dev Dyn. April 1, 2006; 235 (4): 1027-41.
	Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.
	Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.
	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.
	Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development., Baker JC., Genes Dev. December 1, 1999; 13 (23): 3149-59.
	A role for xGCNF in midbrain-hindbrain patterning in Xenopus laevis., Song K., Dev Biol. September 1, 1999; 213 (1): 170-9.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	The role of intracellular alkalinization in the establishment of anterior neural fate in Xenopus., Uzman JA., Dev Biol. January 1, 1998; 193 (1): 10-20.
	Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus., McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Caudalization of neural fate by tissue recombination and bFGF., Cox WG., Development. December 1, 1995; 121 (12): 4349-58.
	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.
	A Xenopus homebox gene defines dorsal-ventral domains in the developing brain., Saha MS., Development. May 1, 1993; 118 (1): 193-202.

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