Papers associated with anterior (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.
	The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programs., Herchenröther A., Nat Commun. January 28, 2023; 14 (1): 472.
	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
	Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
	PDGF-B: The missing piece in the mosaic of PDGF family role in craniofacial development., Corsinovi D., Dev Dyn. July 1, 2019; 248 (7): 603-612.
	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.
	The Ric-8A/Gα13/FAK signalling cascade controls focal adhesion formation during neural crest cell migration in Xenopus., Toro-Tapia G., Development. November 21, 2018; 145 (22):
	MMP14 Regulates Cranial Neural Crest Epithelial-to-Mesenchymal Transition and Migration., Garmon T., Dev Dyn. September 1, 2018; 247 (9): 1083-1092.
	PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.
	Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration., Simon E., Biol Open. October 15, 2017; 6 (10): 1528-1540.
	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.
	Distinct intracellular Ca2+ dynamics regulate apical constriction and differentially contribute to neural tube closure., Suzuki M., Development. April 1, 2017; 144 (7): 1307-1316.
	Elongator Protein 3 (Elp3) stabilizes Snail1 and regulates neural crest migration in Xenopus., Yang X., Sci Rep. May 18, 2016; 6 26238.
	DIPA-family coiled-coils bind conserved isoform-specific head domain of p120-catenin family: potential roles in hydrocephalus and heterotopia., Markham NO., Mol Biol Cell. September 1, 2014; 25 (17): 2592-603.
	Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
	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.
	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.
	CRIM1 complexes with ß-catenin and cadherins, stabilizes cell-cell junctions and is critical for neural morphogenesis., Ponferrada VG., PLoS One. January 1, 2012; 7 (3): e32635.
	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.
	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.
	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.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	Anterior structural defects by misexpression of Xgbx-2 in early Xenopus embryos are associated with altered expression of cell adhesion molecules., King MW, King MW., Dev Dyn. August 1, 1998; 212 (4): 563-79.
	Activities of the Wnt-1 class of secreted signaling factors are antagonized by the Wnt-5A class and by a dominant negative cadherin in early Xenopus development., Torres MA., J Cell Biol. June 1, 1996; 133 (5): 1123-37.
	Cloning and expression studies of cDNA for a novel Xenopus cadherin (XmN-cadherin), expressed maternally and later neural-specifically in embryogenesis., Tashiro K., Mech Dev. February 1, 1996; 54 (2): 161-71.
	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.

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