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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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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.            

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.                        

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.        

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.                        

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.

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.        

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.        

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.              

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

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.      

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

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.                        

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.                

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.                                      

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.  

beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2., Blythe SA, Cha SW, Tadjuidje E, Heasman J, Klein PS., Dev Cell. August 17, 2010; 19 (2): 220-31.      

Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT, Sekkali B, Van Imschoot G, Janssens S, Vleminckx K, Vleminckx K., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.                                                

Residues at the tip of the pore loop of NR3B-containing NMDA receptors determine Ca2+ permeability and Mg2+ block., Cavara NA, Orth A, Hicking G, Seebohm G, Hollmann M., BMC Neurosci. October 19, 2010; 11 133.          

Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST, Milgram SL, Kramer KL, Conlon FL, Moody SA., PLoS One. January 1, 2011; 6 (6): e20309.                  

Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN, Olthoff JT, Matthews AJ, Houston DW., Genesis. March 1, 2011; 49 (3): 117-23.        

An essential role of the cysteine-rich domain of FZD4 in Norrin/Wnt signaling and familial exudative vitreoretinopathy., Zhang K, Harada Y, Wei X, Shukla D, Rajendran A, Tawansy K, Bedell M, Lim S, Shaw PX, He X, Yang Z., J Biol Chem. March 25, 2011; 286 (12): 10210-5.

Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H, López SL, Revinski DR, Carrasco AE., Development. June 1, 2011; 138 (12): 2567-79.                          

The functions of maternal Dishevelled 2 and 3 in the early Xenopus embryo., Tadjuidje E, Cha SW, Louza M, Wylie C, Heasman J., Dev Dyn. July 1, 2011; 240 (7): 1727-36.          

HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ, Wills AE, Chuong E, Gupta R, Baker JC., Genes Dev. August 1, 2011; 25 (15): 1654-61.            

Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S, Cheng F, Liang J, Wu W, Zhang J., PLoS Biol. January 1, 2012; 10 (3): e1001286.                                    

Maternal Wnt/β-catenin signaling coactivates transcription through NF-κB binding sites during Xenopus axis formation., Armstrong NJ, Fagotto F, Prothmann C, Rupp RA., PLoS One. January 1, 2012; 7 (5): e36136.              

Differential role of Axin RGS domain function in Wnt signaling during anteroposterior patterning and maternal axis formation., Schneider PN, Slusarski DC, Houston DW., PLoS One. January 1, 2012; 7 (9): e44096.                

mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells., Miyazaki A, Ishii K, Yamashita S, Nejigane S, Matsukawa S, Ito Y, Onuma Y, Asashima M, Michiue T., PLoS One. January 1, 2012; 7 (10): e46630.        

Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T, Danilchik M, Thumberger T, Vick P, Tisler M, Schneider I, Bogusch S, Andre P, Ulmer B, Walentek P, Niesler B, Blum M, Schweickert A., Curr Biol. January 10, 2012; 22 (1): 33-9.                

Amer2 protein is a novel negative regulator of Wnt/β-catenin signaling involved in neuroectodermal patterning., Pfister AS, Tanneberger K, Schambony A, Behrens J., J Biol Chem. January 13, 2012; 287 (3): 1734-41.      

Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ, Hatayama M, Aruga J., Dev Biol. January 15, 2012; 361 (2): 220-31.                          

Toward an unbiased evolutionary platform for unraveling Xenopus developmental gene networks., Beer R, Wagner F, Grishkevich V, Peshkin L, Yanai I., Genesis. March 1, 2012; 50 (3): 186-91.        

XIAP monoubiquitylates Groucho/TLE to promote canonical Wnt signaling., Hanson AJ, Wallace HA, Freeman TJ, Beauchamp RD, Lee LA, Lee E, Lee E., Mol Cell. March 9, 2012; 45 (5): 619-28.  

Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X, Abreu JG, Yokota C, MacDonald BT, Singh S, Coburn KL, Cheong SM, Zhang MM, Ye QZ, Hang HC, Steen H, He X., Cell. June 22, 2012; 149 (7): 1565-77.                      

Maternal Mga is required for Wnt signaling and organizer formation in the early Xenopus embryo., Gu F, Shi H, Gao L, Zhang H, Tao Q., Acta Biochim Biophys Sin (Shanghai). November 1, 2012; 44 (11): 939-47.

Whole-genome microRNA screening identifies let-7 and mir-18 as regulators of germ layer formation during early embryogenesis., Colas AR, McKeithan WL, Cunningham TJ, Bushway PJ, Garmire LX, Duester G, Subramaniam S, Mercola M., Genes Dev. December 1, 2012; 26 (23): 2567-79.      

An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE, Murgan S, Carrasco AE, López SL., PLoS One. January 1, 2013; 8 (1): e54777.                                      

Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D, Hahn M, Jung J, Schneider TD, Straub T, David R, Schotta G, Rupp RA., PLoS Genet. January 1, 2013; 9 (1): e1003188.                                                                

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

Wnt11b is involved in cilia-mediated symmetry breakage during Xenopus left-right development., Walentek P, Schneider I, Schweickert A, Blum M., PLoS One. January 1, 2013; 8 (9): e73646.              

β-Catenin-independent activation of TCF1/LEF1 in human hematopoietic tumor cells through interaction with ATF2 transcription factors., Grumolato L, Liu G, Haremaki T, Mungamuri SK, Mong P, Akiri G, Lopez-Bergami P, Arita A, Anouar Y, Mlodzik M, Ronai ZA, Brody J, Weinstein DC, Aaronson SA., PLoS Genet. January 1, 2013; 9 (8): e1003603.            

Phosphorylation of Dishevelled by protein kinase RIPK4 regulates Wnt signaling., Huang X, McGann JC, Liu BY, Hannoush RN, Lill JR, Pham V, Newton K, Kakunda M, Liu J, Yu C, Hymowitz SG, Hongo JA, Wynshaw-Boris A, Polakis P, Harland RM, Dixit VM., Science. March 22, 2013; 339 (6126): 1441-5.

Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification., Mei W, Jin Z, Lai F, Schwend T, Houston DW, King ML, Yang J., Development. June 1, 2013; 140 (11): 2334-44.                          

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

Left-right asymmetry: lessons from Cancún., Burdine RD, Caspary T., Development. November 1, 2013; 140 (22): 4465-70.    

Calpain2 protease: A new member of the Wnt/Ca(2+) pathway modulating convergent extension movements in Xenopus., Zanardelli S, Christodoulou N, Skourides PA., Dev Biol. December 1, 2013; 384 (1): 83-100.                        

PTK7 modulates Wnt signaling activity via LRP6., Bin-Nun N, Lichtig H, Malyarova A, Levy M, Elias S, Frank D., Development. January 1, 2014; 141 (2): 410-21.              

Inference of the Xenopus tropicalis embryonic regulatory network and spatial gene expression patterns., Zheng Z, Christley S, Chiu WT, Blitz IL, Xie X, Cho KW, Nie Q., BMC Syst Biol. January 8, 2014; 8 3.                  

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