Papers associated with primary germ layer (and cdh2)

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	In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives., Griffin C., Dev Biol. February 1, 2024; 506 20-30.
	Global analysis of cell behavior and protein dynamics reveals region-specific roles for Shroom3 and N-cadherin during neural tube closure., Baldwin AT., Elife. March 4, 2022; 11
	Non-junctional role of Cadherin3 in cell migration and contact inhibition of locomotion via domain-dependent, opposing regulation of Rac1., Ichikawa T., Sci Rep. October 15, 2020; 10 (1): 17326.
	The transcription factor Hypermethylated in Cancer 1 (Hic1) regulates neural crest migration via interaction with Wnt signaling., Ray H., Dev Biol. July 15, 2020; 463 (2): 169-181.
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	The neural border: Induction, specification and maturation of the territory that generates neural crest cells., Pla P., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.
	Cadherins function during the collective cell migration of Xenopus Cranial Neural Crest cells: revisiting the role of E-cadherin., Cousin H., Mech Dev. December 1, 2017; 148 79-88.
	PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	E-cadherin is required for cranial neural crest migration in Xenopus laevis., Huang C., Dev Biol. March 15, 2016; 411 (2): 159-171.
	Cadherin Switch during EMT in Neural Crest Cells Leads to Contact Inhibition of Locomotion via Repolarization of Forces., Scarpa E., Dev Cell. August 24, 2015; 34 (4): 421-34.
	Role of the hypoxia response pathway in lens formation during embryonic development of Xenopus laevis., Baba K., FEBS Open Bio. October 23, 2013; 3 490-5.
	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.
	Induction of the neural crest state: control of stem cell attributes by gene regulatory, post-transcriptional and epigenetic interactions., Prasad MS., Dev Biol. June 1, 2012; 366 (1): 10-21.
	Cell movements of the deep layer of non-neural ectoderm underlie complete neural tube closure in Xenopus., Morita H., Development. April 1, 2012; 139 (8): 1417-26.
	Regulation of classical cadherin membrane expression and F-actin assembly by alpha-catenins, during Xenopus embryogenesis., Nandadasa S., PLoS One. January 1, 2012; 7 (6): e38756.
	Complement fragment C3a controls mutual cell attraction during collective cell migration., Carmona-Fontaine C., Dev Cell. December 13, 2011; 21 (6): 1026-37.
	Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	Collective chemotaxis requires contact-dependent cell polarity., Theveneau E., Dev Cell. July 20, 2010; 19 (1): 39-53.
	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.
	Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis., Morita H., Development. April 1, 2010; 137 (8): 1315-25.
	Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.
	Stepwise maturation of apicobasal polarity of the neuroepithelium is essential for vertebrate neurulation., Yang X., J Neurosci. September 16, 2009; 29 (37): 11426-40.
	N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	Xenopus cadherin-11 (Xcadherin-11) expression requires the Wg/Wnt signal., Hadeball B., Mech Dev. March 1, 1998; 72 (1-2): 101-13.
	Cadherin-mediated cell interactions are necessary for the activation of MyoD in Xenopus mesoderm., Holt CE., Proc Natl Acad Sci U S A. November 8, 1994; 91 (23): 10844-8.
	Structure and distribution of N-cadherin in developing zebrafish embryos: morphogenetic effects of ectopic over-expression., Bitzur S., Dev Dyn. October 1, 1994; 201 (2): 121-36.
	Selective disruption of E-cadherin function in early Xenopus embryos by a dominant negative mutant., Levine E., Development. April 1, 1994; 120 (4): 901-9.
	Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos., Coffman CR., Cell. May 21, 1993; 73 (4): 659-71.
	N-cadherin transcripts in Xenopus laevis from early tailbud to tadpole., Simonneau L., Dev Dyn. August 1, 1992; 194 (4): 247-60.
	Regulation of embryonic cell adhesion by the cadherin cytoplasmic domain., Kintner C., Cell. April 17, 1992; 69 (2): 225-36.
	Expression of a novel cadherin (EP-cadherin) in unfertilized eggs and early Xenopus embryos., Ginsberg D., Development. February 1, 1991; 111 (2): 315-25.
	Enhanced c-myc gene expression during forelimb regenerative outgrowth in the young Xenopus laevis., Géraudie J., Proc Natl Acad Sci U S A. May 1, 1990; 87 (10): 3797-801.
	The effects of N-cadherin misexpression on morphogenesis in Xenopus embryos., Detrick RJ., Neuron. April 1, 1990; 4 (4): 493-506.
	Cadherin subclasses: differential expression and their roles in neural morphogenesis., Takeichi M., Cold Spring Harb Symp Quant Biol. January 1, 1990; 55 319-25.

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