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Summary Expression Phenotypes Gene Literature (544) GO Terms (6) Nucleotides (117) Proteins (46) Interactants (1444) Wiki
XB--487723

Papers associated with nog (and nodal3.1)



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ccr7 affects both morphogenesis and differentiation during early Xenopus embryogenesis., Goto T, Michiue T, Shibuya H., Dev Growth Differ. June 1, 2022; 64 (5): 254-260.        

Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J, Wielath FM, Vick P., Biol Open. July 15, 2021; 10 (7):                                           

TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M, Amado N, Tan J, Reis A, Ge M, Abreu JG, He X., Elife. September 14, 2020; 9                                                                                           

Natural size variation among embryos leads to the corresponding scaling in gene expression., Leibovich A, Edri T, Klein SL, Moody SA, Fainsod A., Dev Biol. June 15, 2020; 462 (2): 165-179.                    

The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus., Melchert J, Henningfeld KA, Richts S, Lingner T, Jonigk D, Pieler T., Dev Biol. March 15, 2020; 459 (2): 138-148.                                

Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O, Itoh K, Radu A, Ezan J, Sokol SY., Development. January 1, 2020;                                       

RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN, Del Viso F, Duncan AR, Robson A, Hwang W, Kulkarni S, Liu KJ, Liu KJ, Khokha MK., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.                                                

Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N, Chang LS, Koch S, Glinka A, Dolde C, Colozza G, Benitez MDJ, De Robertis EM, Niehrs C., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.                                

Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula., Ding Y, Colozza G, Zhang K, Moriyama Y, Ploper D, Sosa EA, Benitez MDJ, De Robertis EM., Dev Biol. June 15, 2017; 426 (2): 176-187.                                  

Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G, Singhal N, Nicetto D, Straub T, Kremmer E, Rupp RAW., PLoS Genet. May 12, 2017; 13 (5): e1006757.                                    

Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G, Singhal N, Nicetto D, Straub T, Kremmer E, Rupp RAW., PLoS Genet. May 12, 2017; 13 (5): e1006757.                                    

Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y, Ploper D, Sosa EA, Colozza G, Moriyama Y, Benitez MD, Zhang K, Merkurjev D, De Robertis EM., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.                        

Tissue- and stage-specific Wnt target gene expression is controlled subsequent to β-catenin recruitment to cis-regulatory modules., Nakamura Y, de Paiva Alves E, Veenstra GJ, Hoppler S., Development. June 1, 2016; 143 (11): 1914-25.            

A gradient of maternal Bicaudal-C controls vertebrate embryogenesis via translational repression of mRNAs encoding cell fate regulators., Park S, Blaser S, Marchal MA, Houston DW, Sheets MD., Development. March 1, 2016; 143 (5): 864-71.          

Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C, Shi DL., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.            

Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo., Li HY, El Yakoubi W, Shi DL., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.                          

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.              

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.        

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.                          

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.                                                                

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.        

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.                                    

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.                          

A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA, Kormish J, Kofron M, Jegga A, Zorn AM., Dev Biol. March 15, 2011; 351 (2): 297-310.                            

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.                    

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.            

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.            

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.            

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.                

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.              

Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK, Yeh J, Grammer TC, Harland RM., Dev Cell. March 1, 2005; 8 (3): 401-11.                          

Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK, Yeh J, Grammer TC, Harland RM., Dev Cell. March 1, 2005; 8 (3): 401-11.                          

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.                                  

Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H, Wessely O, De Robertis EM., PLoS Biol. May 1, 2004; 2 (5): E92.                

PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J, Wu J, Tan C, Klein PS., Development. December 1, 2003; 130 (23): 5569-78.            

The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB, Kofron M, Tao Q, Tao Q, Schaible K, Wylie C, Heasman J., Development. September 1, 2002; 129 (17): 4027-43.                  

The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM, Itasaki N, Jones CM, Mercurio S, Sargent MG, Smith JC, Krumlauf R., Dev Biol. November 1, 2001; 239 (1): 148-60.              

Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus., Wessely O, Agius E, Oelgeschläger M, Pera EM, De Robertis EM., Dev Biol. June 1, 2001; 234 (1): 161-73.              

Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS, Wilson PA., Dev Biol. June 1, 2001; 234 (1): 42-54.            

foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA, Akers L, Moody SA., Dev Biol. April 15, 2001; 232 (2): 439-57.            

[Neural determination in Xenopus laevis embryos: control of early neural gene expression by calcium]., Leclerc C, Rizzo C, Daguzan C, Néant I, Batut J, Augé B, Moreau M., J Soc Biol. January 1, 2001; 195 (3): 327-37.

FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G, Smith WC., Dev Biol. December 15, 2000; 228 (2): 304-14.            

The Toll/IL-1 receptor binding protein MyD88 is required for Xenopus axis formation., Prothmann C, Armstrong NJ, Rupp RA., Mech Dev. October 1, 2000; 97 (1-2): 85-92.            

The Toll/IL-1 receptor binding protein MyD88 is required for Xenopus axis formation., Prothmann C, Armstrong NJ, Rupp RA., Mech Dev. October 1, 2000; 97 (1-2): 85-92.            

The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD, Hallagan SE, McGrew LL, Miller JR, Moon RT., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.              

Regulation and function of Dlx3 in vertebrate development., Beanan MJ, Sargent TD., Dev Dyn. August 1, 2000; 218 (4): 545-53.      

Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF, Barnett MW, Hartman D, Jones EA, Stott D., Dev Biol. June 15, 2000; 222 (2): 405-19.                  

Primary structure requirements for Xenopus nodal-related 3 and a comparison with regions required by Xenopus nodal-related 2., Ezal CH, Marion CD, Smith WC., J Biol Chem. May 12, 2000; 275 (19): 14124-31.

Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development., Baker JC, Beddington RS, Harland RM., Genes Dev. December 1, 1999; 13 (23): 3149-59.              

Amphibian embryos as a model system for organ engineering: in vitro induction and rescue of the heart anlage., Grunz H., Int J Dev Biol. July 1, 1999; 43 (4): 361-4.        

Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA, Tan C, Conrad LJ, Klein PS., Development. July 1, 1998; 125 (14): 2687-700.                  

The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals., Pannese M, Lupo G, Kablar B, Boncinelli E, Barsacchi G, Vignali R., Mech Dev. April 1, 1998; 73 (1): 73-83.                

Dorsal determinants in the Xenopus egg are firmly associated with the vegetal cortex and behave like activators of the Wnt pathway., Marikawa Y, Li Y, Elinson RP., Dev Biol. November 1, 1997; 191 (1): 69-79.

Markers of vertebrate mesoderm induction., Stennard F, Ryan K, Gurdon JB., Curr Opin Genet Dev. October 1, 1997; 7 (5): 620-7.

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