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Summary Anatomy Item Literature (21411) Expression Attributions Wiki
XB-ANAT-3710

Papers associated with multicellular anatomical structure (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.                                                    


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.                


Molecular markers for corneal epithelial cells in larval vs. adult Xenopus frogs., Sonam S., Exp Eye Res. July 1, 2019; 184 107-125.                        


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.            


Opposite T3 Response of ACTG1-FOS Subnetwork Differentiate Tailfin Fate in Xenopus Tadpole and Post-hatching Axolotl., Kerdivel G., Front Endocrinol (Lausanne). January 25, 2019; 10 194.              


Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.                      


Developmental gene expression patterns in the brain and liver of Xenopus tropicalis during metamorphosis climax., Yaoita Y., Genes Cells. December 1, 2018; 23 (12): 998-1008.              


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.    


MMP14 Regulates Cranial Neural Crest Epithelial-to-Mesenchymal Transition and Migration., Garmon T., Dev Dyn. September 1, 2018; 247 (9): 1083-1092.            


Redistribution of Adhesive Forces through Src/FAK Drives Contact Inhibition of Locomotion in Neural Crest., Roycroft A., Dev Cell. June 4, 2018; 45 (5): 565-579.e3.                                        


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.                                


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.            


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.                                            


Predicting Variabilities in Cardiac Gene Expression with a Boolean Network Incorporating Uncertainty., Grieb M., PLoS One. July 16, 2015; 10 (7): e0131832.        


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.        


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.                        


Activation of voltage gated K⁺ channel Kv1.5 by β-catenin., Munoz C., Biochem Biophys Res Commun. January 13, 2012; 417 (2): 692-6.


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.                        


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.                      


Stimulation of HERG channel activity by β-catenin., Munoz C., PLoS One. January 1, 2012; 7 (8): e43353.          


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.                              


β-catenin is a molecular switch that regulates transition of cell-cell adhesion to fusion., Takezawa Y., Sci Rep. January 1, 2011; 1 68.          


Retinal patterning by Pax6-dependent cell adhesion molecules., Rungger-Brändle E., Dev Neurobiol. September 15, 2010; 70 (11): 764-80.                


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.                      


Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL., Chitalia VC., Nat Cell Biol. October 1, 2008; 10 (10): 1208-16.        


Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.          


Modulation of human Kv1.5 channel kinetics by N-cadherin., Koutsouki E., Biochem Biophys Res Commun. November 9, 2007; 363 (1): 18-23.


Transgenic overexpression of connexin50 induces cataracts., Chung J., Exp Eye Res. March 1, 2007; 84 (3): 513-28.


Expression of N-cadherin, N-CAM, fibronectin and tenascin is stimulated by TGF-beta1, beta2, beta3 and beta5 during the formation of precartilage condensations., Chimal-Monroy J., Int J Dev Biol. January 1, 1999; 43 (1): 59-67.


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.


Xenopus cadherin-11 (Xcadherin-11) expression requires the Wg/Wnt signal., Hadeball B., Mech Dev. March 1, 1998; 72 (1-2): 101-13.        

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