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Summary Expression Phenotypes Gene Literature (217) GO Terms (9) Nucleotides (125) Proteins (57) Interactants (1373) Wiki
XB-GENEPAGE-5964398

Papers associated with nodal3.1



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Homeodomain-interacting protein kinase 2 (HIPK2) targets beta-catenin for phosphorylation and proteasomal degradation., Kim EA, Kim JE, Sung KS, Choi DW, Lee BJ, Choi CY., Biochem Biophys Res Commun. April 16, 2010; 394 (4): 966-71.  


Evidence that fold-change, and not absolute level, of beta-catenin dictates Wnt signaling., Goentoro L, Kirschner MW., Mol Cell. December 11, 2009; 36 (5): 872-84.                                      


Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ, Latinkić BV., PLoS One. October 28, 2009; 4 (10): e7650.                


Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E, Brivanlou AH., J Biol Chem. September 18, 2009; 284 (38): 26127-36.                        


Vegetally localized Xenopus trim36 regulates cortical rotation and dorsal axis formation., Cuykendall TN, Houston DW., Development. September 1, 2009; 136 (18): 3057-65.      


Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation., Koide Y, Kiyota T, Tonganunt M, Pinkaew D, Liu Z, Kato Y, Hutadilok-Towatana N, Phongdara A, Fujise K., Biochim Biophys Acta. May 1, 2009; 1790 (5): 326-38.      


Effects of NR1 splicing on NR1/NR3B-type excitatory glycine receptors., Cavara NA, Orth A, Hollmann M., BMC Neurosci. April 6, 2009; 10 32.      


Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G, Gent YY, Peterson-Maduro J, Verbeek FJ, Destree O., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          


Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH, Yang XY, Conrad WH, Muster J, Angers S, Moon RT, Cheyette BN., PLoS One. January 1, 2009; 4 (2): e4310.                    


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


Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation., Cha SW, Tadjuidje E, Tao Q, Tao Q, Wylie C, Heasman J., Development. November 1, 2008; 135 (22): 3719-29.        


Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL., Chitalia VC, Foy RL, Bachschmid MM, Zeng L, Panchenko MV, Zhou MI, Bharti A, Seldin DC, Lecker SH, Dominguez I, Cohen HT., Nat Cell Biol. October 1, 2008; 10 (10): 1208-16.        


Rules of engagement for NMDA receptor subunits., Ulbrich MH, Isacoff EY., Proc Natl Acad Sci U S A. September 16, 2008; 105 (37): 14163-8.


IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W, Shiojima I, Ito Y, Li Z, Ikeda H, Yoshida M, Naito AT, Nishi J, Ueno H, Umezawa A, Minamino T, Nagai T, Kikuchi A, Asashima M, Komuro I., Nature. July 17, 2008; 454 (7202): 345-9.                        


LRP6 transduces a canonical Wnt signal independently of Axin degradation by inhibiting GSK3's phosphorylation of beta-catenin., Cselenyi CS, Jernigan KK, Tahinci E, Thorne CA, Lee LA, Lee E, Lee E., Proc Natl Acad Sci U S A. June 10, 2008; 105 (23): 8032-7.        


Ectodermal factor restricts mesoderm differentiation by inhibiting p53., Sasai N, Yakura R, Kamiya D, Nakazawa Y, Sasai Y., Cell. May 30, 2008; 133 (5): 878-90.                        


The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB, Harland RM., Dev Dyn. May 1, 2008; 237 (5): 1243-54.            


Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H, Tanegashima K, Ro H, Dawid IB., Development. April 1, 2008; 135 (7): 1283-93.                            


Long- and short-range signals control the dynamic expression of an animal hemisphere-specific gene in Xenopus., Mir A, Kofron M, Heasman J, Mogle M, Lang S, Birsoy B, Wylie C., Dev Biol. March 1, 2008; 315 (1): 161-72.            


Formation of NR1/NR2 and NR1/NR3 heterodimers constitutes the initial step in N-methyl-D-aspartate receptor assembly., Schüler T, Mesic I, Madry C, Bartholomäus I, Laube B., J Biol Chem. January 4, 2008; 283 (1): 37-46.


Modulation of NMDA receptor properties and synaptic transmission by the NR3A subunit in mouse hippocampal and cerebrocortical neurons., Tong G, Takahashi H, Tu S, Shin Y, Talantova M, Zago W, Xia P, Nie Z, Goetz T, Zhang D, Lipton SA, Nakanishi N., J Neurophysiol. January 1, 2008; 99 (1): 122-32.


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.                


Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S, Itasaki N., Dev Biol. October 15, 2007; 310 (2): 250-63.                


Retinoic acid-inducible G protein-coupled receptors bind to frizzled receptors and may activate non-canonical Wnt signaling., Harada Y, Yokota C, Habas R, Slusarski DC, He X., Biochem Biophys Res Commun. July 13, 2007; 358 (4): 968-75.        


Mouse homologues of Shisa antagonistic to Wnt and Fgf signalings., Furushima K, Yamamoto A, Nagano T, Shibata M, Miyachi H, Abe T, Ohshima N, Kiyonari H, Aizawa S., Dev Biol. June 15, 2007; 306 (2): 480-92.  


R-spondin1 is a high affinity ligand for LRP6 and induces LRP6 phosphorylation and beta-catenin signaling., Wei Q, Yokota C, Semenov MV, Doble B, Woodgett J, He X., J Biol Chem. May 25, 2007; 282 (21): 15903-11.  


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


Subunit counting in membrane-bound proteins., Ulbrich MH, Isacoff EY., Nat Methods. April 1, 2007; 4 (4): 319-21.


Principal role of NR3 subunits in NR1/NR3 excitatory glycine receptor function., Madry C, Mesic I, Bartholomäus I, Nicke A, Betz H, Laube B., Biochem Biophys Res Commun. March 2, 2007; 354 (1): 102-8.


Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M, Birsoy B, Houston D, Tao Q, Tao Q, Wylie C, Heasman J., Development. February 1, 2007; 134 (3): 503-13.      


Monomeric mature protein of Nodal-related 3 activates Xbra expression., Haramoto Y, Takahashi S, Asashima M., Dev Genes Evol. January 1, 2007; 217 (1): 29-37.


NR3A modulates the outer vestibule of the "NMDA" receptor channel., Wada A, Takahashi H, Lipton SA, Chen HS., J Neurosci. December 20, 2006; 26 (51): 13156-66.


Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T, Takehara S, Takahashi M, Aizawa S, Yamamoto A., Development. December 1, 2006; 133 (23): 4643-54.                  


Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA, Collart C, Gilchrist MJ, Smith JC., PLoS Genet. November 17, 2006; 2 (11): e193.                                    


Bone density ligand, Sclerostin, directly interacts with LRP5 but not LRP5G171V to modulate Wnt activity., Ellies DL, Viviano B, McCarthy J, Rey JP, Itasaki N, Saunders S, Krumlauf R., J Bone Miner Res. November 1, 2006; 21 (11): 1738-49.              


Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G, Tao Q, Tao Q, Kofron M, Chen JS, Schloemer A, Davis RJ, Hsieh JC, Wylie C, Heasman J, Kuan CY., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.                    


Hex acts with beta-catenin to regulate anteroposterior patterning via a Groucho-related co-repressor and Nodal., Zamparini AL, Watts T, Gardner CE, Tomlinson SR, Johnston GI, Brickman JM., Development. September 1, 2006; 133 (18): 3709-22.                                    


NARF, an nemo-like kinase (NLK)-associated ring finger protein regulates the ubiquitylation and degradation of T cell factor/lymphoid enhancer factor (TCF/LEF)., Yamada M, Ohnishi J, Ohkawara B, Iemura S, Satoh K, Hyodo-Miura J, Kawachi K, Natsume T, Shibuya H., J Biol Chem. July 28, 2006; 281 (30): 20749-20760.                    


Maternal XTcf1 and XTcf4 have distinct roles in regulating Wnt target genes., Standley HJ, Destrée O, Kofron M, Wylie C, Heasman J., Dev Biol. January 15, 2006; 289 (2): 318-28.  


Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation., Wills A, Harland RM, Khokha MK., Dev Biol. January 1, 2006; 289 (1): 166-78.                                  


Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK, Katoh M, Medina A, Steinbeisser H., Cell Commun Signal. October 19, 2005; 3 12.          


Frodo proteins: modulators of Wnt signaling in vertebrate development., Brott BK, Sokol SY., Differentiation. September 1, 2005; 73 (7): 323-9.      


Distinct PAR-1 proteins function in different branches of Wnt signaling during vertebrate development., Ossipova O, Dhawan S, Sokol S, Green JB., Dev Cell. June 1, 2005; 8 (6): 829-41.    


XIC is required for Siamois activity and dorsoanterior development., Snider L, Tapscott SJ., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.


The NR3B subunit does not alter the anesthetic sensitivities of recombinant N-methyl-D-aspartate receptors., Yamakura T, Askalany AR, Petrenko AB, Kohno T, Baba H, Sakimura K., Anesth Analg. June 1, 2005; 100 (6): 1687-1692.


Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos., Tao Q, Tao Q, Yokota C, Puck H, Kofron M, Birsoy B, Yan D, Asashima M, Wylie CC, Lin X, Heasman J., Cell. March 25, 2005; 120 (6): 857-71.            


XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B, Berg L, Williams PH, Smith JC, Wylie CC, Christian JL, Heasman J., Development. February 1, 2005; 132 (3): 591-602.                      


Exploration of the extracellular space by a large-scale secretion screen in the early Xenopus embryo., Pera EM, Hou S, Strate I, Wessely O, De Robertis EM., Int J Dev Biol. January 1, 2005; 49 (7): 781-96.                                  


New roles for FoxH1 in patterning the early embryo., Kofron M, Puck H, Standley H, Wylie C, Old R, Whitman M, Heasman J., Development. October 1, 2004; 131 (20): 5065-78.              


The involvement of Frodo in TCF-dependent signaling and neural tissue development., Hikasa H, Sokol SY., Development. October 1, 2004; 131 (19): 4725-34.      

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