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Summary Expression Phenotypes Gene Literature (500) GO Terms (3) Nucleotides (62) Proteins (38) Interactants (1603) Wiki
XB--483208

Papers associated with nodal



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Xenopus, an ideal model system to study vertebrate left-right asymmetry., Blum M, Beyer T, Weber T, Vick P, Andre P, Bitzer E, Schweickert A., Dev Dyn. June 1, 2009; 238 (6): 1215-25.

Chromatin immunoprecipitation in early Xenopus laevis embryos., Blythe SA, Reid CD, Kessler DS, Klein PS., Dev Dyn. June 1, 2009; 238 (6): 1422-32.

Evolution of leftward flow., Blum M, Weber T, Beyer T, Vick P., Semin Cell Dev Biol. June 1, 2009; 20 (4): 464-71.        

The miR-430/427/302 family controls mesendodermal fate specification via species-specific target selection., Rosa A, Spagnoli FM, Brivanlou AH., Dev Cell. April 1, 2009; 16 (4): 517-27.    

Semiconserved regulation of mesendoderm differentiation by microRNAs., Ketting RF., Dev Cell. April 1, 2009; 16 (4): 487-8.

Cell communication with the neural plate is required for induction of neural markers by BMP inhibition: evidence for homeogenetic induction and implications for Xenopus animal cap and chick explant assays., Linker C, De Almeida I, Papanayotou C, Stower M, Sabado V, Ghorani E, Streit A, Mayor R, Stern CD., Dev Biol. March 15, 2009; 327 (2): 478-86.      

R-spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis Kazanskaya O, Glinka A, del BarcoBarrantes I, Stannek P, Niehrs C, Wu W, Division of Molecular Embryology, Deutsches Krebsforschungszentrum, Heidelberg, Germany., Koeneman KS., Urol Oncol. January 1, 2009; 27 (1):


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.          

GDF3 is a BMP inhibitor that can activate Nodal signaling only at very high doses., Levine AJ, Levine ZJ, Brivanlou AH., Dev Biol. January 1, 2009; 325 (1): 43-8.        

Generating asymmetries in the early vertebrate embryo: the role of the Cerberus-like family., Belo JA, Silva AC, Borges AC, Filipe M, Bento M, Gonçalves L, Vitorino M, Salgueiro AM, Texeira V, Tavares AT, Marques S., Int J Dev Biol. January 1, 2009; 53 (8-10): 1399-407.

Oct25 represses transcription of nodal/activin target genes by interaction with signal transducers during Xenopus gastrulation., Cao Y, Siegel D, Oswald F, Knöchel W., J Biol Chem. December 5, 2008; 283 (49): 34168-77.                

Left-asymmetric expression of Galanin in the linear heart tube of the mouse embryo is independent of the nodal co-receptor gene cryptic., Schweickert A, Deissler K, Britsch S, Albrecht M, Ehmann H, Mauch V, Gaio U, Blum M., Dev Dyn. December 1, 2008; 237 (12): 3557-64.    

Maternal Tgif1 regulates nodal gene expression in Xenopus., Kerr TC, Cuykendall TN, Luettjohann LC, Houston DW., Dev Dyn. October 1, 2008; 237 (10): 2862-73.    

NIP6;1 is a boric acid channel for preferential transport of boron to growing shoot tissues in Arabidopsis., Tanaka M, Wallace IS, Takano J, Roberts DM, Fujiwara T., Plant Cell. October 1, 2008; 20 (10): 2860-75.

Two highly related regulatory subunits of PP2A exert opposite effects on TGF-beta/Activin/Nodal signalling., Batut J, Schmierer B, Cao J, Raftery LA, Hill CS, Howell M., Development. September 1, 2008; 135 (17): 2927-37.  

The pro-domain of the zebrafish Nodal-related protein Cyclops regulates its signaling activities., Tian J, Andrée B, Jones CM, Sampath K., Development. August 1, 2008; 135 (15): 2649-58.  

Regulation of activin/nodal signaling by Rap2-directed receptor trafficking., Choi SC, Kim GH, Lee SJ, Park E, Yeo CY, Han JK., Dev Cell. July 1, 2008; 15 (1): 49-61.

Ventral closure, headfold fusion and definitive endoderm migration defects in mouse embryos lacking the fibronectin leucine-rich transmembrane protein FLRT3., Maretto S, Müller PS, Aricescu AR, Cho KW, Bikoff EK, Robertson EJ., Dev Biol. June 1, 2008; 318 (1): 184-93.

Understanding how morphogens work., Smith JC, Hagemann A, Saka Y, Williams PH., Philos Trans R Soc Lond B Biol Sci. April 12, 2008; 363 (1495): 1387-92.

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.            

Activin/nodal signaling modulates XPAPC expression during Xenopus gastrulation., Lou X, Li S, Wang J, Ding X., Dev Dyn. March 1, 2008; 237 (3): 683-91.        

A perchlorate sensitive iodide transporter in frogs., Carr DL, Carr JA, Willis RE, Pressley TA., Gen Comp Endocrinol. March 1, 2008; 156 (1): 9-14.      

Cripto is a noncompetitive activin antagonist that forms analogous signaling complexes with activin and nodal., Kelber JA, Shani G, Booker EC, Vale WW, Gray PC., J Biol Chem. February 22, 2008; 283 (8): 4490-500.

Coordination of cell polarity during Xenopus gastrulation., Shindo A, Yamamoto TS, Ueno N., PLoS One. February 6, 2008; 3 (2): e1600.              

Expression of Siamois and Twin in the blastula Chordin/Noggin signaling center is required for brain formation in Xenopus laevis embryos., Ishibashi H, Matsumura N, Hanafusa H, Matsumoto K, De Robertis EM, Kuroda H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.              

Unexpected activities of Smad7 in Xenopus mesodermal and neural induction., de Almeida I, Rolo A, Batut J, Hill C, Stern CD, Linker C., Mech Dev. January 1, 2008; 125 (5-6): 421-31.              

Cilia multifunctional organelles at the center of vertebrate left-right asymmetry., Basu B, Brueckner M., Curr Top Dev Biol. January 1, 2008; 85 151-74.

Long-range action of Nodal requires interaction with GDF1., Tanaka C, Sakuma R, Nakamura T, Hamada H, Saijoh Y., Genes Dev. December 15, 2007; 21 (24): 3272-82.        

Nuclear accumulation of Smad complexes occurs only after the midblastula transition in Xenopus., Saka Y, Hagemann AI, Piepenburg O, Smith JC., Development. December 1, 2007; 134 (23): 4209-18.

Developmental biology: micro(RNA)-managing nodal., Martin BL, Kimelman D., Curr Biol. November 20, 2007; 17 (22): R975-7.

Regulation of the response to Nodal-mediated mesoderm induction by Xrel3., Kennedy MW, Green KA, Ford RL, Andrews PG, Paterno GD, Gillespie LL, Kao KR., Dev Biol. November 15, 2007; 311 (2): 383-95.      

Distinct and cooperative roles of mammalian Vg1 homologs GDF1 and GDF3 during early embryonic development., Andersson O, Bertolino P, Ibáñez CF., Dev Biol. November 15, 2007; 311 (2): 500-11.

Two T-box genes play independent and cooperative roles to regulate morphogenesis of ciliated Kupffer's vesicle in zebrafish., Amack JD, Wang X, Yost HJ., Dev Biol. October 15, 2007; 310 (2): 196-210.    

Tsukushi modulates Xnr2, FGF and BMP signaling: regulation of Xenopus germ layer formation., Morris SA, Almeida AD, Tanaka H, Ohta K, Ohnuma S., PLoS One. October 10, 2007; 2 (10): e1004.                    

The role of FoxC1 in early Xenopus development., Cha JY, Birsoy B, Kofron M, Mahoney E, Lang S, Wylie C, Heasman J., Dev Dyn. October 1, 2007; 236 (10): 2731-41.        

XSUMO-1 is required for normal mesoderm induction and axis elongation during early Xenopus development., Yukita A, Michiue T, Danno H, Asashima M., Dev Dyn. October 1, 2007; 236 (10): 2757-66.    

The role of maternal Activin-like signals in zebrafish embryos., Hagos EG, Fan X, Dougan ST., Dev Biol. September 15, 2007; 309 (2): 245-58.

MicroRNA control of Nodal signalling., Martello G, Zacchigna L, Inui M, Montagner M, Adorno M, Mamidi A, Morsut L, Soligo S, Tran U, Dupont S, Cordenonsi M, Wessely O, Piccolo S., Nature. September 13, 2007; 449 (7159): 183-8.

Xenopus Lefty requires proprotein cleavage but not N-linked glycosylation to inhibit nodal signaling., Westmoreland JJ, Takahashi S, Wright CV., Dev Dyn. August 1, 2007; 236 (8): 2050-61.        

TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S, Morokuma J, Hayata T, Kolle G, Niehrs C, Ueno N, Cho KW., Genes Dev. July 15, 2007; 21 (14): 1817-31.                  

The Sox axis, Nodal signaling, and germ layer specification., Zhang C, Klymkowsky MW., Differentiation. July 1, 2007; 75 (6): 536-45.          

The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V, Reversade B, De Robertis EM., EMBO J. June 20, 2007; 26 (12): 2955-65.              

Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant., Fein AJ, Meadows LS, Chen C, Slat EA, Isom LL., BMC Genomics. May 16, 2007; 8 226.                      

The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B, Moody SA., Dev Biol. May 1, 2007; 305 (1): 103-19.        

Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan., Coolen M, Sauka-Spengler T, Nicolle D, Le-Mentec C, Lallemand Y, Da Silva C, Plouhinec JL, Robert B, Wincker P, Shi DL, Mazan S., PLoS One. April 18, 2007; 2 (4): e374.              

CHD4/Mi-2beta activity is required for the positioning of the mesoderm/neuroectoderm boundary in Xenopus., Linder B, Mentele E, Mansperger K, Straub T, Kremmer E, Rupp RA., Genes Dev. April 15, 2007; 21 (8): 973-83.            

Endofin acts as a Smad anchor for receptor activation in BMP signaling., Shi W, Chang C, Nie S, Xie S, Wan M, Cao X., J Cell Sci. April 1, 2007; 120 (Pt 7): 1216-24.

Multiple functions of Cerberus cooperate to induce heart downstream of Nodal., Foley AC, Korol O, Timmer AM, Mercola M., Dev Biol. March 1, 2007; 303 (1): 57-65.        

The evolutionally conserved activity of Dapper2 in antagonizing TGF-beta signaling., Su Y, Zhang L, Gao X, Meng F, Wen J, Zhou H, Meng A, Chen YG., FASEB J. March 1, 2007; 21 (3): 682-90.

PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM, Mei W, Liette NL, Phiel C, El-Hodiri HM, Yang J., Dev Biol. February 15, 2007; 302 (2): 477-93.                  

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