Papers associated with primary germ layer (and en1)

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	Injury-induced Erk1/2 signaling tissue-specifically interacts with Ca2+ activity and is necessary for regeneration of spinal cord and skeletal muscle., Levin JB., Cell Calcium. March 1, 2022; 102 102540.
	Bioinformatics Screening of Genes Specific for Well-Regenerating Vertebrates Reveals c-answer, a Regulator of Brain Development and Regeneration., Korotkova DD., Cell Rep. October 22, 2019; 29 (4): 1027-1040.e6.
	A model for investigating developmental eye repair in Xenopus laevis., Kha CX., Exp Eye Res. April 1, 2018; 169 38-47.
	RARβ2 is required for vertebrate somitogenesis., Janesick A., Development. June 1, 2017; 144 (11): 1997-2008.
	Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability., Twigg SR., Am J Hum Genet. September 3, 2015; 97 (3): 378-88.
	Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome., Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57.
	Transient downregulation of Bmp signalling induces extra limbs in vertebrates., Christen B., Development. July 1, 2012; 139 (14): 2557-65.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Lymph heart musculature is under distinct developmental control from lymphatic endothelium., Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.
	Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.
	Neogenin and RGMa control neural tube closure and neuroepithelial morphology by regulating cell polarity., Kee N., J Neurosci. November 26, 2008; 28 (48): 12643-53.
	Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	Hedgehog regulation of superficial slow muscle fibres in Xenopus and the evolution of tetrapod trunk myogenesis., Grimaldi A., Development. July 1, 2004; 131 (14): 3249-62.
	Primitive roles for inhibitory interneurons in developing frog spinal cord., Li WC., J Neurosci. June 23, 2004; 24 (25): 5840-8.
	Differential gene expression between the embryonic tail bud and regenerating larval tail in Xenopus laevis., Sugiura T., Dev Growth Differ. February 1, 2004; 46 (1): 97-105.
	Xenopus eomesodermin is expressed in neural differentiation., Ryan K., Mech Dev. July 1, 1998; 75 (1-2): 155-8.
	Comparative analysis of Engrailed-1 and Wnt-1 expression in the developing central nervous system of Xenopus laevis., Eizema K., Int J Dev Biol. December 1, 1994; 38 (4): 623-32.
	Examining pattern formation in mouse, chicken and frog embryos with an En-specific antiserum., Davis CA., Development. February 1, 1991; 111 (2): 287-98.

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