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Summary Anatomy Item Literature (100) Expression Attributions Wiki
ECB-ANAT-55

Papers associated with vegetal plate

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The evolution of a new cell type was associated with competition for a signaling ligand., Ettensohn CA., PLoS Biol. September 18, 2019; 17 (9): e3000460.                    


Spatial and temporal patterns of gene expression during neurogenesis in the sea urchin Lytechinus variegatus., Slota LA., Evodevo. January 1, 2019; 10 2.              


Theoretical tool bridging cell polarities with development of robust morphologies., Nissen SB., Elife. November 27, 2018; 7                                         


Morphological diversity of blastula formation and gastrulation in temnopleurid sea urchins., Kitazawa C., Biol Open. November 15, 2016; 5 (11): 1555-1566.                    


Eph and Ephrin function in dispersal and epithelial insertion of pigmented immunocytes in sea urchin embryos., Krupke OA., Elife. July 30, 2016; 5               


Cooperative Wnt-Nodal Signals Regulate the Patterning of Anterior Neuroectoderm., Yaguchi J., PLoS Genet. April 21, 2016; 12 (4): e1006001.                


Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks., Dylus DV., Evodevo. January 1, 2016; 7 2.            


Experimental Approach Reveals the Role of alx1 in the Evolution of the Echinoderm Larval Skeleton., Koga H., PLoS One. January 1, 2016; 11 (2): e0149067.          


Heterologous expression of newly identified galectin-8 from sea urchin embryos produces recombinant protein with lactose binding specificity and anti-adhesive activity., Karakostis K., Sci Rep. December 7, 2015; 5 17665.            


Jun N-terminal kinase activity is required for invagination but not differentiation of the sea urchin archenteron., Long JT., Genesis. December 1, 2015; 53 (12): 762-9.


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


Logics and properties of a genetic regulatory program that drives embryonic muscle development in an echinoderm., Andrikou C., Elife. July 28, 2015; 4                                       


bicaudal-C is required for the formation of anterior neurogenic ectoderm in the sea urchin embryo., Yaguchi S., Sci Rep. October 31, 2014; 4 6852.            


Restricted expression of karyopherin alpha mRNA in the sea urchin suggests a role in neurogenesis., Byrum CA., Gene Expr Patterns. September 1, 2014; 16 (1): 51-60.


Myogenesis in the sea urchin embryo: the molecular fingerprint of the myoblast precursors., Andrikou C., Evodevo. December 2, 2013; 4 (1): 33.              


Growth attenuation with developmental schedule progression in embryos and early larvae of Sterechinus neumayeri raised under elevated CO2., Yu PC., PLoS One. January 1, 2013; 8 (1): e52448.              


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


Morphogenesis in sea urchin embryos: linking cellular events to gene regulatory network states., Lyons DC., Wiley Interdiscip Rev Dev Biol. January 1, 2012; 1 (2): 231-52.


Atypical protein kinase C controls sea urchin ciliogenesis., Prulière G., Mol Biol Cell. June 15, 2011; 22 (12): 2042-53.                


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


Involvement of Delta and Nodal signals in the specification process of five types of secondary mesenchyme cells in embryo of the sea urchin, Hemicentrotus pulcherrimus., Ohguro Y., Dev Growth Differ. January 1, 2011; 53 (1): 110-23.


Uncoupling of complex regulatory patterning during evolution of larval development in echinoderms., Yankura KA., BMC Biol. November 30, 2010; 8 143.          


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


Suppressor of Hairless (Su(H)) is required for foregut development in the sea urchin embryo., Karasawa K., Zoolog Sci. October 1, 2009; 26 (10): 686-90.


Gene regulatory network subcircuit controlling a dynamic spatial pattern of signaling in the sea urchin embryo., Smith J., Proc Natl Acad Sci U S A. December 23, 2008; 105 (51): 20089-94.


Expression patterns of three Par-related genes in sea urchin embryos., Shiomi K., Gene Expr Patterns. May 1, 2008; 8 (5): 323-30.


Ingression of primary mesenchyme cells of the sea urchin embryo: a precisely timed epithelial mesenchymal transition., Wu SY., Birth Defects Res C Embryo Today. December 1, 2007; 81 (4): 241-52.


Gene expression patterns in a novel animal appendage: the sea urchin pluteus arm., Love AC., Evol Dev. January 1, 2007; 9 (1): 51-68.


Germ line determinants are not localized early in sea urchin development, but do accumulate in the small micromere lineage., Juliano CE., Dev Biol. December 1, 2006; 300 (1): 406-15.


Expression of Spgatae, the Strongylocentrotus purpuratus ortholog of vertebrate GATA4/5/6 factors., Lee PY., Gene Expr Patterns. December 1, 2004; 5 (2): 161-5.


Gastrulation in the sea urchin embryo: a model system for analyzing the morphogenesis of a monolayered epithelium., Kominami T., Dev Growth Differ. August 1, 2004; 46 (4): 309-26.


Pigment cells trigger the onset of gastrulation in tropical sea urchin Echinometra mathaei., Takata H., Dev Growth Differ. February 1, 2004; 46 (1): 23-35.


Nuclear localization of beta-catenin in vegetal pole cells during early embryogenesis of the starfish Asterina pectinifera., Miyawaki K., Dev Growth Differ. April 1, 2003; 45 (2): 121-8.


Primary mesenchyme cell patterning during the early stages following ingression., Peterson RE., Dev Biol. February 1, 2003; 254 (1): 68-78.


Behavior and differentiation process of pigment cells in a tropical sea urchin Echinometra mathaei., Takata H., Dev Growth Differ. January 1, 2003; 45 (5-6): 473-83.


Inhibition of mitogen activated protein kinase signaling affects gastrulation and spiculogenesis in the sea urchin embryo., Kumano M., Dev Growth Differ. January 1, 2003; 45 (5-6): 527-42.


SpADAM, a sea urchin ADAM, has conserved structure and expression., Rise M., Mech Dev. September 1, 2002; 117 (1-2): 275-81.


The expression of SpRunt during sea urchin embryogenesis., Robertson AJ., Mech Dev. September 1, 2002; 117 (1-2): 327-30.


brachyury Target genes in the early sea urchin embryo isolated by differential macroarray screening., Rast JP., Dev Biol. June 1, 2002; 246 (1): 191-208.


A regulatory gene network that directs micromere specification in the sea urchin embryo., Oliveri P., Dev Biol. June 1, 2002; 246 (1): 209-28.


Behavior of pigment cells in gastrula-stage embryos of Hemicentrotus pulcherrimus and Scaphechinus mirabilis., Kominami T., Dev Growth Differ. December 1, 2001; 43 (6): 699-707.


Correct Expression of spec2a in the sea urchin embryo requires both Otx and other cis-regulatory elements., Yuh CH., Dev Biol. April 15, 2001; 232 (2): 424-38.


Brachyury homolog (HpTa) is involved in the formation of archenteron and secondary mesenchyme cell differentiation in the sea urchin embryo., Mitsunaga-Nakatsubo K., Zoology (Jena). January 1, 2001; 104 (2): 99-102.


Transcriptional regulation of the gene for epidermal growth factor-like peptides in sea urchin embryos., Yamasu K., Int J Dev Biol. October 1, 2000; 44 (7): 777-84.


Primary mesenchyme cell-ring pattern formation in 2D-embryos of the sea urchin., Katow H., Dev Growth Differ. February 1, 2000; 42 (1): 9-17.


A starfish homolog of mouse T-brain-1 is expressed in the archenteron of Asterina pectinifera embryos: possible involvement of two T-box genes in starfish gastrulation., Shoguchi E., Dev Growth Differ. February 1, 2000; 42 (1): 61-8.


Characterization of a hemichordate fork head/HNF-3 gene expression., Taguchi S., Dev Genes Evol. January 1, 2000; 210 (1): 11-7.


Modularity and dissociation in the evolution of gene expression territories in development., Raff RA., Evol Dev. January 1, 2000; 2 (2): 102-13.


Studies on the cellular basis of morphogenesis in the sea urchin embryo. Directed movements of primary mesenchyme cells in normal and vegetalized larvae., Gustafson T., Exp Cell Res. December 15, 1999; 253 (2): 288-95.


Cell movements in the sea urchin embryo., Ettensohn CA., Curr Opin Genet Dev. August 1, 1999; 9 (4): 461-5.

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