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Summary Anatomy Item Literature (1058) Expression Attributions Wiki
XB-ANAT-4103

Papers associated with septum (and snai2)

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Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              

GSK3 and Polo-like kinase regulate ADAM13 function during cranial neural crest cell migration., Abbruzzese G., Mol Biol Cell. December 15, 2014; 25 (25): 4072-82.                                    

Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.                              

A noncanonical Frizzled2 pathway regulates epithelial-mesenchymal transition and metastasis., Gujral TS., Cell. November 6, 2014; 159 (4): 844-56.              

The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.                            

In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity., Kuriyama S., J Cell Biol. July 7, 2014; 206 (1): 113-27.                                

Role of the Rap2/TNIK kinase pathway in regulation of LRP6 stability for Wnt signaling., Park DS., Biochem Biophys Res Commun. June 28, 2013; 436 (2): 338-43.        

Calponin 2 acts as an effector of noncanonical Wnt-mediated cell polarization during neural crest cell migration., Ulmer B., Cell Rep. March 28, 2013; 3 (3): 615-21.              

Xnr3 affects brain patterning via cell migration in the neural-epidermal tissue boundary during early Xenopus embryogenesis., Morita M., Int J Dev Biol. January 1, 2013; 57 (9-10): 779-86.          

Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.                  

Cloning and spatiotemporal expression of RIC-8 in Xenopus embryogenesis., Maldonado-Agurto R., Gene Expr Patterns. October 1, 2011; 11 (7): 401-8.          

V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.                        

Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.                    

Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9.                                    

XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms., van Grunsven LA., Dev Biol. June 1, 2007; 306 (1): 34-49.            

Cardiac neural crest ablation alters Id2 gene expression in the developing heart., Martinsen BJ., Dev Biol. August 1, 2004; 272 (1): 176-90.          

Wise, a context-dependent activator and inhibitor of Wnt signalling., Itasaki N., Development. September 1, 2003; 130 (18): 4295-305.                

Expression of Xenopus snail in mesoderm and prospective neural fold ectoderm., Essex LJ., Dev Dyn. October 1, 1993; 198 (2): 108-22.              

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