Papers associated with axial mesoderm (and odc1)

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	Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):
	Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula., Ding Y., Dev Biol. June 15, 2017; 426 (2): 176-187.
	Centrin-2 (Cetn2) mediated regulation of FGF/FGFR gene expression in Xenopus., Shi J., Sci Rep. May 27, 2015; 5 10283.
	Sulf1 has ligand-dependent effects on canonical and non-canonical Wnt signalling., Fellgett SW., J Cell Sci. April 1, 2015; 128 (7): 1408-21.
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS., Cell Rep. February 3, 2015; 10 (4): 527-36.
	The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.
	A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance., Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	The secreted integrin ligand nephronectin is necessary for forelimb formation in Xenopus tropicalis., Abu-Daya A., Dev Biol. January 15, 2011; 349 (2): 204-12.
	XIer2 is required for convergent extension movements during Xenopus development., Hong SK., Int J Dev Biol. January 1, 2011; 55 (10-12): 917-21.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation., Inomata H., Cell. September 5, 2008; 134 (5): 854-65.
	XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation., Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.
	Developmental expression of Shisa-2 in Xenopus laevis., Silva AC., Int J Dev Biol. January 1, 2006; 50 (6): 575-9.
	Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation., Leise WF., Development. April 1, 2004; 131 (8): 1703-15.
	Overexpression of the secreted factor Mig30 expressed in the Spemann organizer impairs morphogenetic movements during Xenopus gastrulation., Hayata T., Mech Dev. March 1, 2002; 112 (1-2): 37-51.
	The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW., Dev Biol. October 15, 2001; 238 (2): 303-14.
	Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.
	A role for GATA5 in Xenopus endoderm specification., Weber H., Development. October 1, 2000; 127 (20): 4345-60.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	Nodal-related signals induce axial mesoderm and dorsalize mesoderm during gastrulation., Jones CM., Development. November 1, 1995; 121 (11): 3651-62.

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