Papers associated with LOC587482 (and LOC105441782)

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	Protein degradation machinery is present broadly during early development in the sea urchin., Zazueta-Novoa V, Wessel GM., Gene Expr Patterns. July 1, 2014; 15 (2): 135-41.
	The DEAD-box helicase Vasa: evidence for a multiplicity of functions in RNA processes and developmental biology., Lasko P., Biochim Biophys Acta. August 1, 2013; 1829 (8): 810-6.
	The DEAD-box RNA helicase Vasa functions in embryonic mitotic progression in the sea urchin., Yajima M, Wessel GM., Development. June 1, 2011; 138 (11): 2217-22.
	Post-translational regulation by gustavus contributes to selective Vasa protein accumulation in multipotent cells during embryogenesis., Gustafson EA, Yajima M, Juliano CE, Wessel GM., Dev Biol. January 15, 2011; 349 (2): 440-50.
	Isolation of oogonia from ovaries of the sea urchin Strongylocentrotus nudus., Yakovlev KV, Battulin NR, Serov OL, Odintsova NA., Cell Tissue Res. December 1, 2010; 342 (3): 479-90.
	An evolutionary transition of Vasa regulation in echinoderms., Juliano CE, Wessel GM., Evol Dev. January 1, 2009; 11 (5): 560-73.
	Vasa protein expression is restricted to the small micromeres of the sea urchin, but is inducible in other lineages early in development., Voronina E, Lopez M, Juliano CE, Gustafson E, Song JL, Extavour C, George S, Oliveri P, McClay D, Wessel G., Dev Biol. February 15, 2008; 314 (2): 276-86.
	Patterns of gene expression in the developing adult sea urchin central nervous system reveal multiple domains and deep-seated neural pentamery., Sly BJ, Hazel JC, Popodi EM, Raff RA., Evol Dev. January 1, 2002; 4 (3): 189-204.

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