Papers associated with lefty1

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	Nodal and BMP2/4 signaling organizes the oral-aboral axis of the sea urchin embryo., Duboc V, Röttinger E, Besnardeau L, Lepage T., Dev Cell. March 1, 2004; 6 (3): 397-410.
	RTK and TGF-beta signaling pathways genes in the sea urchin genome., Lapraz F, Röttinger E, Duboc V, Range R, Duloquin L, Walton K, Wu SY, Bradham C, Loza MA, Hibino T, Wilson K, Poustka A, McClay D, Angerer L, Gache C, Lepage T., Dev Biol. December 1, 2006; 300 (1): 132-52.
	A conserved role for the nodal signaling pathway in the establishment of dorso-ventral and left-right axes in deuterostomes., Duboc V, Lepage T., J Exp Zool B Mol Dev Evol. January 15, 2008; 310 (1): 41-53.
	Lefty acts as an essential modulator of Nodal activity during sea urchin oral-aboral axis formation., Duboc V, Lapraz F, Besnardeau L, Lepage T., Dev Biol. August 1, 2008; 320 (1): 49-59.
	Mitochondria and metazoan epigenesis., Coffman JA., Semin Cell Dev Biol. May 1, 2009; 20 (3): 321-9.
	TGFβ signaling positions the ciliary band and patterns neurons in the sea urchin embryo., Yaguchi S, Yaguchi J, Angerer RC, Angerer LM, Burke RD., Dev Biol. November 1, 2010; 347 (1): 71-81.
	Ancestral regulatory circuits governing ectoderm patterning downstream of Nodal and BMP2/4 revealed by gene regulatory network analysis in an echinoderm., Saudemont A, Haillot E, Mekpoh F, Bessodes N, Quirin M, Lapraz F, Duboc V, Röttinger E, Range R, Oisel A, Besnardeau L, Wincker P, Lepage T., PLoS Genet. December 23, 2010; 6 (12): e1001259.
	Nodal-mediated epigenesis requires dynamin-mediated endocytosis., Ertl RP, Robertson AJ, Saunders D, Coffman JA., Dev Dyn. March 1, 2011; 240 (3): 704-11.
	Reciprocal signaling between the ectoderm and a mesendodermal left-right organizer directs left-right determination in the sea urchin embryo., Bessodes N, Haillot E, Duboc V, Röttinger E, Lahaye F, Lepage T., PLoS Genet. January 1, 2012; 8 (12): e1003121.
	A detailed description of the development of the hemichordate Saccoglossus kowalevskii using SEM, TEM, Histology and 3D-reconstructions., Kaul-Strehlow S, Stach T., Front Zool. September 6, 2013; 10 (1): 53.
	An essential role for maternal control of Nodal signaling., Kumari P, Gilligan PC, Lim S, Tran LD, Winkler S, Philp R, Sampath K., Elife. September 10, 2013; 2 e00683.
	Oral-aboral axis specification in the sea urchin embryo, IV: hypoxia radializes embryos by preventing the initial spatialization of nodal activity., Coffman JA, Wessels A, DeSchiffart C, Rydlizky K., Dev Biol. February 15, 2014; 386 (2): 302-7.
	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.
	Mechanisms of the epithelial-to-mesenchymal transition in sea urchin embryos., Katow H., Tissue Barriers. January 1, 2015; 3 (4): e1059004.
	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, Molina MD, Lapraz F, Lepage T., 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, Haillot E, Lepage T., Nat Commun. October 1, 2015; 6 8434.
	Hemichordate genomes and deuterostome origins., Simakov O, Kawashima T, Marlétaz F, Jenkins J, Koyanagi R, Mitros T, Hisata K, Bredeson J, Shoguchi E, Gyoja F, Yue JX, Chen YC, Freeman RM, Sasaki A, Hikosaka-Katayama T, Sato A, Fujie M, Baughman KW, Levine J, Gonzalez P, Cameron C, Fritzenwanker JH, Pani AM, Goto H, Kanda M, Arakaki N, Yamasaki S, Qu J, Cree A, Ding Y, Dinh HH, Dugan S, Holder M, Jhangiani SN, Kovar CL, Lee SL, Lewis LR, Morton D, Nazareth LV, Okwuonu G, Santibanez J, Chen R, Richards S, Muzny DM, Gillis A, Peshkin L, Wu M, Humphreys T, Su YH, Putnam NH, Schmutz J, Fujiyama A, Yu JK, Tagawa K, Worley KC, Gibbs RA, Kirschner MW, Lowe CJ, Satoh N, Rokhsar DS, Gerhart J., Nature. November 26, 2015; 527 (7579): 459-65.
	Cooperative Wnt-Nodal Signals Regulate the Patterning of Anterior Neuroectoderm., Yaguchi J, Takeda N, Inaba K, Yaguchi S., PLoS Genet. April 21, 2016; 12 (4): e1006001.
	Acquisition of the dorsal structures in chordate amphioxus., Morov AR, Ukizintambara T, Sabirov RM, Yasui K., Open Biol. June 1, 2016; 6 (6):
	Nodal and BMP expression during the transition to pentamery in the sea urchin Heliocidaris erythrogramma: insights into patterning the enigmatic echinoderm body plan., Koop D, Cisternas P, Morris VB, Strbenac D, Yang JY, Wray GA, Byrne M., BMC Dev Biol. February 13, 2017; 17 (1): 4.
	Troponin-I is present as an essential component of muscles in echinoderm larvae., Yaguchi S, Yaguchi J, Tanaka H., Sci Rep. March 8, 2017; 7 43563.
	Hedgehog participates in the establishment of left-right asymmetry during amphioxus development by controlling Cerberus expression., Hu G, Li G, Wang H, Wang Y., Development. December 15, 2017; 144 (24): 4694-4703.
	Nodal induces sequential restriction of germ cell factors during primordial germ cell specification., Fresques TM, Wessel GM., Development. January 22, 2018; 145 (2):
	Transforming growth factor-β signal regulates gut bending in the sea urchin embryo., Suzuki H, Yaguchi S., Dev Growth Differ. May 1, 2018; 60 (4): 216-225.
	MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo., Molina MD, Quirin M, Haillot E, De Crozé N, Range R, Rouel M, Jimenez F, Amrouche R, Chessel A, Lepage T., PLoS Genet. September 17, 2018; 14 (9): e1007621.
	Coup-TF: A maternal factor essential for differentiation along the embryonic axes in the sea urchin Paracentrotus lividus., Tsironis I, Paganos P, Gouvi G, Tsimpos P, Stamopoulou A, Arnone MI, Flytzanis CN., Dev Biol. July 1, 2021; 475 131-144.

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