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Logics and properties of a genetic regulatory program that drives embryonic muscle development in an echinoderm. , Andrikou C., Elife. July 28, 2015; 4
A sea urchin Na(+)K(+)2Cl(-) cotransporter is involved in the maintenance of calcification-relevant cytoplasmic cords in Strongylocentrotus droebachiensis larvae. , Basse WC., Comp Biochem Physiol A Mol Integr Physiol. September 1, 2015; 187 184-92.
Carbonic anhydrase inhibition blocks skeletogenesis and echinochrome production in Paracentrotus lividus and Heliocidaris tuberculata embryos and larvae. , Zito F., Dev Growth Differ. September 1, 2015; 57 (7): 507-14.
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., PLoS Biol. September 9, 2015; 13 (9): e1002247.
A deuterostome origin of the Spemann organiser suggested by Nodal and ADMPs functions in Echinoderms. , Lapraz F., Nat Commun. October 1, 2015; 6 8434.
H(+)/K(+) ATPase activity is required for biomineralization in sea urchin embryos. , Schatzberg D., Dev Biol. October 15, 2015; 406 (2): 259-70.
microRNA-31 modulates skeletal patterning in the sea urchin embryo. , Stepicheva NA., Development. November 1, 2015; 142 (21): 3769-80.
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.
RNA-Seq identifies SPGs as a ventral skeletal patterning cue in sea urchins. , Piacentino ML., Development. February 15, 2016; 143 (4): 703-14.
Zygotic LvBMP5-8 is required for skeletal patterning and for left-right but not dorsal-ventral specification in the sea urchin embryo. , Piacentino ML., Dev Biol. April 1, 2016; 412 (1): 44-56.
Characterization of an Alpha Type Carbonic Anhydrase from Paracentrotus lividus Sea Urchin Embryos. , Karakostis K., Mar Biotechnol (NY). June 1, 2016; 18 (3): 384-95.
Morphological diversity of blastula formation and gastrulation in temnopleurid sea urchins. , Kitazawa C., Biol Open. November 15, 2016; 5 (11): 1555-1566.
The small GTPase Arf6 regulates sea urchin morphogenesis. , Stepicheva NA., Differentiation. January 1, 2017; 95 31-43.
KirrelL, a member of the Ig-domain superfamily of adhesion proteins, is essential for fusion of primary mesenchyme cells in the sea urchin embryo. , Ettensohn CA ., Dev Biol. January 15, 2017; 421 (2): 258-270.
TGF-β sensu stricto signaling regulates skeletal morphogenesis in the sea urchin embryo. , Sun Z., Dev Biol. January 15, 2017; 421 (2): 149-160.
A sea urchin in vivo model to evaluate Epithelial-Mesenchymal Transition. , Romancino DP., Dev Growth Differ. April 1, 2017; 59 (3): 141-151.
Characterization and expression analysis of Galnts in developing Strongylocentrotus purpuratus embryos. , Famiglietti AL., PLoS One. April 17, 2017; 12 (4): e0176479.
Alteration of neurotransmission and skeletogenesis in sea urchin Arbacia lixula embryos exposed to copper oxide nanoparticles. , Cappello T., Comp Biochem Physiol C Toxicol Pharmacol. September 1, 2017; 199 20-27.
Endocytosis in primary mesenchyme cells during sea urchin larval skeletogenesis. , Killian CE ., Exp Cell Res. October 1, 2017; 359 (1): 205-214.
Functional divergence of paralogous transcription factors supported the evolution of biomineralization in echinoderms. , Khor JM., Elife. November 20, 2017; 6
Developmental effects of the protein kinase inhibitor kenpaullone on the sea urchin embryo. , Anello L., Comp Biochem Physiol C Toxicol Pharmacol. January 1, 2018; 204 36-44.
Thyroid Hormones Accelerate Initiation of Skeletogenesis via MAPK ( ERK1/2) in Larval Sea Urchins (Strongylocentrotus purpuratus). , Taylor E., Front Endocrinol (Lausanne). January 1, 2018; 9 439.
Transforming a transcription factor. , Burke RD ., Elife. January 8, 2018; 7
Global analysis of primary mesenchyme cell cis-regulatory modules by chromatin accessibility profiling. , Shashikant T., BMC Genomics. March 20, 2018; 19 (1): 206.
A SLC4 family bicarbonate transporter is critical for intracellular pH regulation and biomineralization in sea urchin embryos. , Hu MY ., Elife. May 1, 2018; 7
Cdc42 controls primary mesenchyme cell morphogenesis in the sea urchin embryo. , Sepúlveda-Ramírez SP., Dev Biol. May 15, 2018; 437 (2): 140-151.
Inhibition of microRNA suppression of Dishevelled results in Wnt pathway-associated developmental defects in sea urchin. , Sampilo NF., Development. November 30, 2018; 145 (23):
Culture of and experiments with sea urchin embryo primary mesenchyme cells. , Moreno B., Methods Cell Biol. January 1, 2019; 150 293-330.
Measurement of feeding rates, respiration, and pH regulatory processes in the light of ocean acidification research. , Stumpp M., Methods Cell Biol. January 1, 2019; 150 391-409.
Spatially mapping gene expression in sea urchin primary mesenchyme cells. , Zuch DT., Methods Cell Biol. January 1, 2019; 151 433-442.
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.