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Summary Anatomy Item Literature (10392) Expression Attributions Wiki
XB-ANAT-111

Papers associated with embryo (and krt8.1)

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Mechanical and signaling roles for keratin intermediate filaments in the assembly and morphogenesis of Xenopus mesendoderm tissue at gastrulation., Sonavane PR., Development. December 1, 2017; 144 (23): 4363-4376.                            


Clustered Xenopus keratin genes: A genomic, transcriptomic, and proteomic analysis., Suzuki KT., Dev Biol. June 15, 2017; 426 (2): 384-392.


Global analysis of asymmetric RNA enrichment in oocytes reveals low conservation between closely related Xenopus species., Claußen M., Mol Biol Cell. November 5, 2015; .            


Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3., Juraver-Geslin HA., Genesis. February 1, 2015; 53 (2): 203-24.          


FAK is required for tension-dependent organization of collective cell movements in Xenopus mesendoderm., Bjerke MA., Dev Biol. October 15, 2014; 394 (2): 340-56.                        


Custos controls β-catenin to regulate head development during vertebrate embryogenesis., Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.                                


Interrogating transcriptional regulatory sequences in Tol2-mediated Xenopus transgenics., Loots GG., PLoS One. July 1, 2013; 8 (7): e68548.          


Upon Wnt stimulation, Rac1 activation requires Rac1 and Vav2 binding to p120-catenin., Valls G., J Cell Sci. November 15, 2012; 125 (Pt 22): 5288-301.                


A mechanoresponsive cadherin-keratin complex directs polarized protrusive behavior and collective cell migration., Weber GF., Dev Cell. January 17, 2012; 22 (1): 104-15.            


Inhibition of GSK3 phosphorylation of beta-catenin via phosphorylated PPPSPXS motifs of Wnt coreceptor LRP6., Wu G., PLoS One. January 1, 2009; 4 (3): e4926.              


Direct inhibition of GSK3beta by the phosphorylated cytoplasmic domain of LRP6 in Wnt/beta-catenin signaling., Piao S., PLoS One. January 1, 2008; 3 (12): e4046.          


Beta-arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo., Bryja V., Proc Natl Acad Sci U S A. April 17, 2007; 104 (16): 6690-5.  


Macroarray-based analysis of tail regeneration in Xenopus laevis larvae., Tazaki A., Dev Dyn. August 1, 2005; 233 (4): 1394-404.                          


Microarray-based identification of VegT targets in Xenopus., Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.                                          


Physiological regulation of [beta]-catenin stability by Tcf3 and CK1epsilon., Lee E, Lee E., J Cell Biol. September 3, 2001; 154 (5): 983-93.                


Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.                                                            


Occludin dephosphorylation in early development of Xenopus laevis., Cordenonsi M., J Cell Sci. December 1, 1997; 110 ( Pt 24) 3131-9.                


Modified mRNA rescue of maternal CK1/8 mRNA depletion in Xenopus oocytes., Raats JM., Antisense Nucleic Acid Drug Dev. August 1, 1997; 7 (4): 263-77.


Distinct distribution of vimentin and cytokeratin in Xenopus oocytes and early embryos., Torpey NP., J Cell Sci. January 1, 1992; 101 ( Pt 1) 151-60.                


Identification of vimentin and novel vimentin-related proteins in Xenopus oocytes and early embryos., Torpey NP., Development. December 1, 1990; 110 (4): 1185-95.            

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