Papers associated with archenteron (and myod1)

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	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	dmrt2 and myf5 Link Early Somitogenesis to Left-Right Axis Determination in Xenopus laevis., Tingler M., Front Cell Dev Biol. January 1, 2022; 10 858272.
	FGF-mediated establishment of left-right asymmetry requires Rab7 function in the dorsal mesoderm in Xenopus., Kreis J., Front Cell Dev Biol. January 1, 2022; 10 981762.
	Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5., Maerker M., Nat Commun. September 16, 2021; 12 (1): 5482.
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Furry is required for cell movements during gastrulation and functionally interacts with NDR1., Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
	Mechanical strain, novel genes and evolutionary insights: news from the frog left-right organizer., Blum M., Curr Opin Genet Dev. June 1, 2019; 56 8-14.
	A dual function of FGF signaling in Xenopus left-right axis formation., Schneider I., Development. May 10, 2019; 146 (9):
	The extraordinary biology and development of marsupial frogs (Hemiphractidae) in comparison with fish, mammals, birds, amphibians and other animals., Del Pino EM., Mech Dev. December 1, 2018; 154 2-11.
	Candidate Heterotaxy Gene FGFR4 Is Essential for Patterning of the Left-Right Organizer in Xenopus., Sempou E., Front Physiol. January 1, 2018; 9 1705.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
	On the origin of vertebrate somites., Onai T., Zoological Lett. June 15, 2015; 1 33.
	TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus., Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.
	Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	The nodal inhibitor Coco is a critical target of leftward flow in Xenopus., Schweickert A., Curr Biol. April 27, 2010; 20 (8): 738-43.
	Delta-Notch signaling is involved in the segregation of the three germ layers in Xenopus laevis., Revinski DR., Dev Biol. March 15, 2010; 339 (2): 477-92.
	The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.
	Developmental expression of Shisa-2 in Xenopus laevis., Silva AC., Int J Dev Biol. January 1, 2006; 50 (6): 575-9.
	Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity., Yabe S., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.
	An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N., Mech Dev. March 1, 2005; 122 (3): 365-439.
	Redundant early and overlapping larval roles of Xsox17 subgroup genes in Xenopus endoderm development., Clements D., Mech Dev. March 1, 2003; 120 (3): 337-48.
	Xenopus kielin: A dorsalizing factor containing multiple chordin-type repeats secreted from the embryonic midline., Matsui M., Proc Natl Acad Sci U S A. May 9, 2000; 97 (10): 5291-6.
	Cadherin-mediated cell interactions are necessary for the activation of MyoD in Xenopus mesoderm., Holt CE., Proc Natl Acad Sci U S A. November 8, 1994; 91 (23): 10844-8.
	Expression of XMyoD protein in early Xenopus laevis embryos., Hopwood ND., Development. January 1, 1992; 114 (1): 31-8.
	Xenopus Myf-5 marks early muscle cells and can activate muscle genes ectopically in early embryos., Hopwood ND., Development. February 1, 1991; 111 (2): 551-60.

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