Papers associated with LOC587482 (and LOC100887844)

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	Translational Control of Canonical and Non-Canonical Translation Initiation Factors at the Sea Urchin Egg to Embryo Transition., Chassé H, Boulben S, Cormier P, Morales J., Int J Mol Sci. February 1, 2019; 20 (3):
	A K(+)-selective CNG channel orchestrates Ca(2+) signalling in zebrafish sperm., Fechner S, Alvarez L, Bönigk W, Müller A, Berger TK, Pascal R, Trötschel C, Poetsch A, Stölting G, Siegfried KR, Kremmer E, Seifert R, Kaupp UB., Elife. December 9, 2015; 4
	Essential elements for translation: the germline factor Vasa functions broadly in somatic cells., Yajima M, Wessel GM., Development. June 1, 2015; 142 (11): 1960-70.
	Two-pore channels provide insight into the evolution of voltage-gated Ca2+ and Na+ channels., Rahman T, Cai X, Brailoiu GC, Abood ME, Brailoiu E, Patel S., Sci Signal. November 18, 2014; 7 (352): ra109.
	Hypoxia-modulated gene expression profiling in sea urchin (Strongylocentrotus nudus) immune cells., Suh SS, Hwang J, Park M, Park SY, Ryu TK, Lee S, Lee TK., Ecotoxicol Environ Saf. November 1, 2014; 109 63-9.
	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.
	Helitron Transposons on the Sex Chromosomes of the Platyfish Xiphophorus maculatus and Their Evolution in Animal Genomes., Zhou Q, Froschauer A, Schultheis C, Schmidt C, Bienert GP, Wenning M, Dettai A, Volff JN., Zebrafish. January 1, 2006; 3 (1): 39-52.
	Contrahelicase activity of the mitochondrial transcription termination factor mtDBP., Polosa PL, Deceglie S, Roberti M, Gadaleta MN, Cantatore P., Nucleic Acids Res. July 8, 2005; 33 (12): 3812-20.
	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.
	DNA-helicase activity from sea urchin mitochondria., Roberti M, Musicco C, Polosa PL, Gadaleta MN, Cantatore P., Biochem Biophys Res Commun. February 6, 1996; 219 (1): 134-9.

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