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Summary Expression Phenotypes Gene Literature (38) GO Terms (10) Nucleotides (446) Proteins (68) Interactants (409) Wiki
XB-GENEPAGE-489396

Papers associated with jup



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Genome-wide identification of thyroid hormone receptor targets in the remodeling intestine during Xenopus tropicalis metamorphosis., Fu L, Das B, Matsuura K, Fujimoto K, Heimeier RA, Shi YB, Shi YB., Sci Rep. July 25, 2017; 7 (1): 6414.            


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


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


Genomic targets of Brachyury (T) in differentiating mouse embryonic stem cells., Evans AL, Faial T, Gilchrist MJ, Down T, Vallier L, Pedersen RA, Wardle FC, Smith JC., PLoS One. January 1, 2012; 7 (3): e33346.              


Sox17 and Sox4 differentially regulate beta-catenin/T-cell factor activity and proliferation of colon carcinoma cells., Sinner D, Kordich JJ, Spence JR, Opoka R, Rankin S, Rankin S, Lin SC, Jonatan D, Zorn AM, Wells JM., Mol Cell Biol. November 1, 2007; 27 (22): 7802-15.                


A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y, Smith JC., Dev Biol. September 15, 2004; 273 (2): 210-25.                      


Sox17 and beta-catenin cooperate to regulate the transcription of endodermal genes., Sinner D, Rankin S, Rankin S, Lee M, Zorn AM., Development. July 1, 2004; 131 (13): 3069-80.                      


Regulation of apoptosis in theXenopus embryo by Bix3., Trindade M, Messenger N, Papin C, Grimmer D, Fairclough L, Tada M, Smith JC., Development. October 1, 2003; 130 (19): 4611-22.                  


Plakoglobin is required for maintenance of the cortical actin skeleton in early Xenopus embryos and for cdc42-mediated wound healing., Kofron M, Heasman J, Lang SA, Wylie CC., J Cell Biol. August 19, 2002; 158 (4): 695-708.                  


Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach., Heasman J, Kofron M, Wylie C., Dev Biol. June 1, 2000; 222 (1): 124-34.        


Depression in the level of cadherin and alpha-, beta-, gamma-catenins in transgenic Xenopus laevis highly expressing c-Src., Dvoráková K, Habrová V, Takác M, Jonák J., Folia Biol (Praha). January 1, 2000; 46 (1): 3-9.


Membrane-anchored plakoglobins have multiple mechanisms of action in Wnt signaling., Klymkowsky MW, Williams BO, Barish GD, Varmus HE, Vourgourakis YE., Mol Biol Cell. October 1, 1999; 10 (10): 3151-69.


Immunocytochemical studies of the interactions of cadherins and catenins in the early Xenopus embryo., Kurth T, Fesenko IV, Schneider S, Münchberg FE, Joos TO, Spieker TP, Hausen P., Dev Dyn. June 1, 1999; 215 (2): 155-69.


Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF, Fang X, Ji H, Reynolds AB, McCrea PD., Dev Biol. March 15, 1999; 207 (2): 350-63.            


Membrane-tethered Drosophila Armadillo cannot transduce Wingless signal on its own., Cox RT, Pai LM, Miller JR, Orsulic S, Stein J, McCormick CA, Audeh Y, Wang W, Moon RT, Peifer M., Development. March 1, 1999; 126 (6): 1327-35.


Yel013p (Vac8p), an armadillo repeat protein related to plakoglobin and importin alpha is associated with the yeast vacuole membrane., Fleckenstein D, Rohde M, Klionsky DJ, Rüdiger M., J Cell Sci. October 1, 1998; 111 ( Pt 20) 3109-18.


Expression of the Armadillo family member p120cas1B in Xenopus embryos affects head differentiation but not axis formation., Geis K, Aberle H, Kühl M, Kemler R, Wedlich D., Dev Genes Evol. January 1, 1998; 207 (7): 471-81.


Plakophilins 1a and 1b: widespread nuclear proteins recruited in specific epithelial cells as desmosomal plaque components., Schmidt A, Langbein L, Rode M, Prätzel S, Zimbelmann R, Franke WW., Cell Tissue Res. December 1, 1997; 290 (3): 481-99.


Analysis of the signaling activities of localization mutants of beta-catenin during axis specification in Xenopus., Miller JR, Moon RT., J Cell Biol. October 6, 1997; 139 (1): 229-43.                


Cytoplasmically anchored plakoglobin induces a WNT-like phenotype in Xenopus., Merriam JM, Rubenstein AB, Klymkowsky MW., Dev Biol. May 1, 1997; 185 (1): 67-81.              


The roles of maternal alpha-catenin and plakoglobin in the early Xenopus embryo., Kofron M, Spagnuolo A, Klymkowsky M, Wylie C, Heasman J., Development. April 1, 1997; 124 (8): 1553-60.        


Localizing the adhesive and signaling functions of plakoglobin., Rubenstein A, Merriam J, Klymkowsky MW., Dev Genet. January 1, 1997; 20 (2): 91-102.


beta-Catenin associates with the actin-bundling protein fascin in a noncadherin complex., Tao YS, Edwards RA, Tubb B, Wang S, Bryan J, McCrea PD., J Cell Biol. September 1, 1996; 134 (5): 1271-81.


Desmosomal cadherin binding domains of plakoglobin., Witcher LL, Collins R, Puttagunta S, Mechanic SE, Munson M, Gumbiner B, Cowin P., J Biol Chem. May 3, 1996; 271 (18): 10904-9.


Anterior axis duplication in Xenopus induced by the over-expression of the cadherin-binding protein plakoglobin., Karnovsky A, Klymkowsky MW., Proc Natl Acad Sci U S A. May 9, 1995; 92 (10): 4522-6.


Cell type-specific desmosomal plaque proteins of the plakoglobin family: plakophilin 1 (band 6 protein)., Heid HW, Schmidt A, Zimbelmann R, Schäfer S, Winter-Simanowski S, Stumpp S, Keith M, Figge U, Schnölzer M, Franke WW., Differentiation. December 1, 1994; 58 (2): 113-31.


Induction of a secondary body axis in Xenopus by antibodies to beta-catenin., McCrea PD, Brieher WM, Gumbiner BM., J Cell Biol. October 1, 1993; 123 (2): 477-84.


Responses to Wnt signals in vertebrate embryos may involve changes in cell adhesion and cell movement., Moon RT, DeMarais A, Olson DJ., J Cell Sci Suppl. January 1, 1993; 17 183-8.    


Catenins as mediators of the cytoplasmic functions of cadherins., Gumbiner BM, McCrea PD., J Cell Sci Suppl. January 1, 1993; 17 155-8.


p120, a novel substrate of protein tyrosine kinase receptors and of p60v-src, is related to cadherin-binding factors beta-catenin, plakoglobin and armadillo., Reynolds AB, Herbert L, Cleveland JL, Berg ST, Gaut JR., Oncogene. December 1, 1992; 7 (12): 2439-45.


Identification of plakoglobin in oocytes and early embryos of Xenopus laevis: maternal expression of a gene encoding a junctional plaque protein., Fouquet B, Zimbelmann R, Franke WW., Differentiation. November 1, 1992; 51 (3): 187-94.


The armadillo homologs beta-catenin and plakoglobin are differentially expressed during early development of Xenopus laevis., DeMarais AA, Moon RT., Dev Biol. October 1, 1992; 153 (2): 337-46.          


Plakoglobin and beta-catenin: distinct but closely related., Butz S, Stappert J, Weissig H, Kemler R., Science. August 21, 1992; 257 (5073): 1142-4.


The vertebrate adhesive junction proteins beta-catenin and plakoglobin and the Drosophila segment polarity gene armadillo form a multigene family with similar properties., Peifer M, McCrea PD, Green KJ, Wieschaus E, Gumbiner BM., J Cell Biol. August 1, 1992; 118 (3): 681-91.


A homolog of the armadillo protein in Drosophila (plakoglobin) associated with E-cadherin., McCrea PD, Turck CW, Gumbiner B., Science. November 29, 1991; 254 (5036): 1359-61.


The uvomorulin-anchorage protein alpha catenin is a vinculin homologue., Herrenknecht K, Ozawa M, Eckerskorn C, Lottspeich F, Lenter M, Kemler R., Proc Natl Acad Sci U S A. October 15, 1991; 88 (20): 9156-60.


Cytokeratin filaments and desmosomes in the epithelioid cells of the perineurial and arachnoidal sheaths of some vertebrate species., Achtstätter T, Fouquet B, Rungger-Brändle E, Franke WW., Differentiation. May 1, 1989; 40 (2): 129-49.                        


Cytoskeletons of retinal pigment epithelial cells: interspecies differences of expression patterns indicate independence of cell function from the specific complement of cytoskeletal proteins., Owaribe K, Kartenbeck J, Rungger-Brändle E, Franke WW., Cell Tissue Res. November 1, 1988; 254 (2): 301-15.

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