Papers associated with LOC115926321 (and LOC115919910)

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	Global analysis of primary mesenchyme cell cis-regulatory modules by chromatin accessibility profiling., Shashikant T, Khor JM, Ettensohn CA., BMC Genomics. March 20, 2018; 19 (1): 206.
	Characterization and expression analysis of Galnts in developing Strongylocentrotus purpuratus embryos., Famiglietti AL, Wei Z, Beres TM, Milac AL, Tran DT, Patel D, Angerer RC, Angerer LM, Tabak LA., PLoS One. April 17, 2017; 12 (4): e0176479.
	Expression and Prognostic Relevance of GAGE1 and XAGE1 Cancer/Testis Antigens in Head and Neck Squamous Cell Carcinoma., Karia BTR, Zamuner FT, Carlin V, de Oliveira CZ, Carvalho AL, Vettore AL., Curr Mol Med. January 1, 2017; 17 (10): 707-717.
	bicaudal-C is required for the formation of anterior neurogenic ectoderm in the sea urchin embryo., Yaguchi S, Yaguchi J, Inaba K., Sci Rep. October 31, 2014; 4 6852.
	Gene regulatory network interactions in sea urchin endomesoderm induction., Sethi AJ, Angerer RC, Angerer LM., PLoS Biol. February 3, 2009; 7 (2): e1000029.
	A global view of gene expression in lithium and zinc treated sea urchin embryos: new components of gene regulatory networks., Poustka AJ, Kühn A, Groth D, Weise V, Yaguchi S, Burke RD, Herwig R, Lehrach H, Panopoulou G., Genome Biol. January 1, 2007; 8 (5): R85.
	Endo16 is required for gastrulation in the sea urchin Lytechinus variegatus., Romano LA, Wray GA., Dev Growth Differ. October 1, 2006; 48 (8): 487-97.
	Brn1/2/4, the predicted midgut regulator of the endo16 gene of the sea urchin embryo., Yuh CH, Dorman ER, Davidson EH., Dev Biol. May 15, 2005; 281 (2): 286-98.
	Conservation of Endo16 expression in sea urchins despite evolutionary divergence in both cis and trans-acting components of transcriptional regulation., Romano LA, Wray GA., Development. September 1, 2003; 130 (17): 4187-99.
	Evidence for a mesodermal embryonic regulator of the sea urchin CyIIa gene., Martin EL, Consales C, Davidson EH, Arnone MI., Dev Biol. August 1, 2001; 236 (1): 46-63.
	Correct Expression of spec2a in the sea urchin embryo requires both Otx and other cis-regulatory elements., Yuh CH, Li X, Davidson EH, Klein WH., Dev Biol. April 15, 2001; 232 (2): 424-38.
	Cis-regulation downstream of cell type specification: a single compact element controls the complex expression of the CyIIa gene in sea urchin embryos., Arnone MI, Martin EL, Davidson EH., Development. April 1, 1998; 125 (8): 1381-95.
	Specification of endoderm in the sea urchin embryo., Godin RE, Klinzing DC, Porcaro WA, Ernst SG., Mech Dev. September 1, 1997; 67 (1): 35-47.
	Quantitative functional interrelations within the cis-regulatory system of the S. purpuratus Endo16 gene., Yuh CH, Moore JG, Davidson EH., Development. December 1, 1996; 122 (12): 4045-56.
	Molecular cloning, characterization, and genetic mapping of the cDNA coding for a novel secretory protein of mouse. Demonstration of alternative splicing in skin and cartilage., Bhalerao J, Tylzanowski P, Filie JD, Kozak CA, Merregaert J., J Biol Chem. July 7, 1995; 270 (27): 16385-94.
	Endo16, a large multidomain protein found on the surface and ECM of endodermal cells during sea urchin gastrulation, binds calcium., Soltysik-Española M, Klinzing DC, Pfarr K, Burke RD, Ernst SG., Dev Biol. September 1, 1994; 165 (1): 73-85.
	Altered cell fate in LiCl-treated sea urchin embryos., Nocente-McGrath C, McIsaac R, Ernst SG., Dev Biol. October 1, 1991; 147 (2): 445-50.
	Endo16, a lineage-specific protein of the sea urchin embryo, is first expressed just prior to gastrulation., Nocente-McGrath C, Brenner CA, Ernst SG., Dev Biol. November 1, 1989; 136 (1): 264-72.

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