Papers associated with sensory system (and hand2)

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	Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish., Bisgrove BW., Elife. November 15, 2017; 6
	Noggin is required for first pharyngeal arch differentiation in the frog Xenopus tropicalis., Young JJ., Dev Biol. June 15, 2017; 426 (2): 245-254.
	CUG-BP, Elav-like family member 1 (CELF1) is required for normal myofibrillogenesis, morphogenesis, and contractile function in the embryonic heart., Blech-Hermoni Y., Dev Dyn. August 1, 2016; 245 (8): 854-73.
	A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements., Square T., Dev Biol. January 15, 2015; 397 (2): 293-304.
	Ascl1 as a novel player in the Ptf1a transcriptional network for GABAergic cell specification in the retina., Mazurier N., PLoS One. March 18, 2014; 9 (3): e92113.
	Serotonin 2B receptor signaling is required for craniofacial morphogenesis and jaw joint formation in Xenopus., Reisoli E., Development. September 1, 2010; 137 (17): 2927-37.
	Xenopus zinc finger transcription factor IA1 (Insm1) expression marks anteroventral noradrenergic neuron progenitors in Xenopus embryos., Parlier D., Dev Dyn. August 1, 2008; 237 (8): 2147-57.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	The mych gene is required for neural crest survival during zebrafish development., Hong SK., PLoS One. April 9, 2008; 3 (4): e2029.
	Conservation of sequence and expression of Xenopus and zebrafish dHAND during cardiac, branchial arch and lateral mesoderm development., Angelo S., Mech Dev. July 1, 2000; 95 (1-2): 231-7.

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