Papers associated with mesoderm (and cdh1)

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	The Wnt/PCP formin Daam1 drives cell-cell adhesion during nephron development., Krneta-Stankic V., Cell Rep. July 6, 2021; 36 (1): 109340.
	Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
	Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation., Nasr T., Dev Cell. December 16, 2019; 51 (6): 665-674.e6.
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	The atypical mitogen-activated protein kinase ERK3 is essential for establishment of epithelial architecture., Takahashi C., J Biol Chem. June 1, 2018; 293 (22): 8342-8361.
	Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling., Vacca B., Sci Rep. January 19, 2018; 8 (1): 1204.
	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.
	A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates., Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
	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.
	Caspase-9 has a nonapoptotic function in Xenopus embryonic primitive blood formation., Tran HT., J Cell Sci. July 15, 2017; 130 (14): 2371-2381.
	Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2., Scerbo P., Elife. June 27, 2017; 6
	Folate receptor 1 is necessary for neural plate cell apical constriction during Xenopus neural tube formation., Balashova OA., Development. April 15, 2017; 144 (8): 1518-1530.
	Role of JNK during buccopharyngeal membrane perforation, the last step of embryonic mouth formation., Houssin NS., Dev Dyn. February 1, 2017; 246 (2): 100-115.
	Syndecan4 coordinates Wnt/JNK and BMP signaling to regulate foregut progenitor development., Zhang Z, Zhang Z., Dev Biol. August 1, 2016; 416 (1): 187-199.
	E-cadherin is required for cranial neural crest migration in Xenopus laevis., Huang C., Dev Biol. March 15, 2016; 411 (2): 159-171.
	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.
	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.
	Paraxis is required for somite morphogenesis and differentiation in Xenopus laevis., Sánchez RS., Dev Dyn. August 1, 2015; 244 (8): 973-87.
	Myocyte enhancer factor 2D regulates ectoderm specification and adhesion properties of animal cap cells in the early Xenopus embryo., Katz Imberman S., FEBS J. August 1, 2015; 282 (15): 2930-47.
	A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance., Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Different thresholds of Wnt-Frizzled 7 signaling coordinate proliferation, morphogenesis and fate of endoderm progenitor cells., Zhang Z., Dev Biol. June 1, 2013; 378 (1): 1-12.
	The hypoxia factor Hif-1α controls neural crest chemotaxis and epithelial to mesenchymal transition., Barriga EH., J Cell Biol. May 27, 2013; 201 (5): 759-76.
	Jun N-terminal kinase maintains tissue integrity during cell rearrangement in the gut., Dush MK., Development. April 1, 2013; 140 (7): 1457-66.
	The Mix family of homeobox genes--key regulators of mesendoderm formation during vertebrate development., Pereira LA., Dev Biol. July 15, 2012; 367 (2): 163-77.
	fus/TLS orchestrates splicing of developmental regulators during gastrulation., Dichmann DS., Genes Dev. June 15, 2012; 26 (12): 1351-63.
	Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo., Ninomiya H., J Cell Sci. April 15, 2012; 125 (Pt 8): 1877-83.
	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.
	Transcriptional activation by Oct4 is sufficient for the maintenance and induction of pluripotency., Hammachi F., Cell Rep. February 23, 2012; 1 (2): 99-109.
	Foxi2 is an animally localized maternal mRNA in Xenopus, and an activator of the zygotic ectoderm activator Foxi1e., Cha SW., PLoS One. January 1, 2012; 7 (7): e41782.
	Dystroglycan is involved in skin morphogenesis downstream of the Notch signaling pathway., Sirour C., Mol Biol Cell. August 15, 2011; 22 (16): 2957-69.
	IGF-1 increases invasive potential of MCF 7 breast cancer cells and induces activation of latent TGF-β1 resulting in epithelial to mesenchymal transition., Walsh LA., Cell Commun Signal. May 2, 2011; 9 (1): 10.
	B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.
	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.
	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.
	Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex., Verstappen G., Hum Mol Genet. April 15, 2008; 17 (8): 1175-83.
	Medial cell mixing during axial morphogenesis of the amphibian embryo requires cadherin function., Delarue M., Dev Dyn. November 1, 1998; 213 (3): 248-60.
	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.
	Molecular cloning of cDNA for XTCAD-1, a novel Xenopus cadherin, and its expression in adult tissues and embryos of Xenopus laevis., Tooi O., Biochim Biophys Acta. September 13, 1994; 1219 (1): 121-8.
	Regulation of C-cadherin function during activin induced morphogenesis of Xenopus animal caps., Brieher WM., J Cell Biol. July 1, 1994; 126 (2): 519-27.
	Catenins in Xenopus embryogenesis and their relation to the cadherin-mediated cell-cell adhesion system., Schneider S., Development. June 1, 1993; 118 (2): 629-40.
	EP-cadherin in muscles and epithelia of Xenopus laevis embryos., Levi G., Development. December 1, 1991; 113 (4): 1335-44.
	Differential expression of two cadherins in Xenopus laevis., Angres B., Development. March 1, 1991; 111 (3): 829-44.
	The distribution of E-cadherin during Xenopus laevis development., Levi G., Development. January 1, 1991; 111 (1): 159-69.
	Identification of Ca2(+)-dependent cell adhesion molecules in Xenopus by the use of interspecies homology., Herzberg F., Differentiation. July 1, 1990; 44 (1): 1-7.
	Expression of cell adhesion molecule E-cadherin in Xenopus embryos begins at gastrulation and predominates in the ectoderm., Choi YS., J Cell Biol. June 1, 1989; 108 (6): 2449-58.

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