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Summary Expression Gene Literature (90) GO Terms (2) Nucleotides (13) Proteins (7) Interactants (206) Wiki
ECB--23036620

Papers associated with nodall (and pole)



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MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo., Molina MD, Quirin M, Haillot E, De Crozé N, Range R, Rouel M, Jimenez F, Amrouche R, Chessel A, Lepage T., PLoS Genet. September 17, 2018; 14 (9): e1007621.                


Cilia are required for asymmetric nodal induction in the sea urchin embryo., Tisler M, Wetzel F, Mantino S, Kremnyov S, Thumberger T, Schweickert A, Blum M, Vick P., BMC Dev Biol. August 23, 2016; 16 (1): 28.        


Acquisition of the dorsal structures in chordate amphioxus., Morov AR, Ukizintambara T, Sabirov RM, Yasui K., Open Biol. June 1, 2016; 6 (6):                 


A deuterostome origin of the Spemann organiser suggested by Nodal and ADMPs functions in Echinoderms., Lapraz F, Haillot E, Lepage T., Nat Commun. October 1, 2015; 6 8434.                    


The Maternal Maverick/GDF15-like TGF-β Ligand Panda Directs Dorsal-Ventral Axis Formation by Restricting Nodal Expression in the Sea Urchin Embryo., Haillot E, Molina MD, Lapraz F, Lepage T., PLoS Biol. September 9, 2015; 13 (9): e1002247.                      


A detailed description of the development of the hemichordate Saccoglossus kowalevskii using SEM, TEM, Histology and 3D-reconstructions., Kaul-Strehlow S, Stach T., Front Zool. September 6, 2013; 10 (1): 53.                            


Integration of canonical and noncanonical Wnt signaling pathways patterns the neuroectoderm along the anterior-posterior axis of sea urchin embryos., Range RC, Angerer RC, Angerer LM., PLoS Biol. January 1, 2013; 11 (1): e1001467.              


Left-right asymmetry in the sea urchin embryo: BMP and the asymmetrical origins of the adult., Warner JF, Lyons DC, McClay DR., PLoS Biol. January 1, 2012; 10 (10): e1001404.  


Reciprocal signaling between the ectoderm and a mesendodermal left-right organizer directs left-right determination in the sea urchin embryo., Bessodes N, Haillot E, Duboc V, Röttinger E, Lahaye F, Lepage T., PLoS Genet. January 1, 2012; 8 (12): e1003121.                      


Novel population of embryonic secondary mesenchyme cells in the keyhole sand dollar Astriclypeus manni., Takata H, Kominami T., Dev Growth Differ. June 1, 2011; 53 (5): 625-38.


Ancestral regulatory circuits governing ectoderm patterning downstream of Nodal and BMP2/4 revealed by gene regulatory network analysis in an echinoderm., Saudemont A, Haillot E, Mekpoh F, Bessodes N, Quirin M, Lapraz F, Duboc V, Röttinger E, Range R, Oisel A, Besnardeau L, Wincker P, Lepage T., PLoS Genet. December 23, 2010; 6 (12): e1001259.                      


Patterning of the dorsal-ventral axis in echinoderms: insights into the evolution of the BMP-chordin signaling network., Lapraz F, Besnardeau L, Lepage T., PLoS Biol. November 1, 2009; 7 (11): e1000248.                        


The sea urchin animal pole domain is a Six3-dependent neurogenic patterning center., Wei Z, Yaguchi J, Yaguchi S, Angerer RC, Angerer LM., Development. April 1, 2009; 136 (7): 1179-89.


Specification of ectoderm restricts the size of the animal plate and patterns neurogenesis in sea urchin embryos., Yaguchi S, Yaguchi J, Burke RD., Development. June 1, 2006; 133 (12): 2337-46.


Nodal signaling and the evolution of deuterostome gastrulation., Chea HK, Wright CV, Swalla BJ., Dev Dyn. October 1, 2005; 234 (2): 269-78.


Oral-aboral axis specification in the sea urchin embryo II. Mitochondrial distribution and redox state contribute to establishing polarity in Strongylocentrotus purpuratus., Coffman JA, McCarthy JJ, Dickey-Sims C, Robertson AJ., Dev Biol. September 1, 2004; 273 (1): 160-71.

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