Papers associated with blastopore (and fgf2)

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	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):
	Rspo2 antagonizes FGF signaling during vertebrate mesoderm formation and patterning., Reis AH., Development. May 27, 2020; 147 (10):
	Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;
	Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
	Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos., Lee SY., Differentiation. September 1, 2011; 82 (2): 99-107.
	Isthmin is a novel secreted angiogenesis inhibitor that inhibits tumour growth in mice., Xiang W., J Cell Mol Med. February 1, 2011; 15 (2): 359-74.
	Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network., de Crozé N., Proc Natl Acad Sci U S A. January 4, 2011; 108 (1): 155-60.
	Downstream of FGF during mesoderm formation in Xenopus: the roles of Elk-1 and Egr-1., Nentwich O., Dev Biol. December 15, 2009; 336 (2): 313-26.
	The RNA-binding protein Mex3b has a fine-tuning system for mRNA regulation in early Xenopus development., Takada H., Development. July 1, 2009; 136 (14): 2413-22.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.
	Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
	Antagonistic interaction between IGF and Wnt/JNK signaling in convergent extension in Xenopus embryo., Carron C., Mech Dev. November 1, 2005; 122 (11): 1234-47.
	FGF signal interpretation is directed by Sprouty and Spred proteins during mesoderm formation., Sivak JM., Dev Cell. May 1, 2005; 8 (5): 689-701.
	Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.
	Neural induction requires BMP inhibition only as a late step, and involves signals other than FGF and Wnt antagonists., Linker C., Development. November 1, 2004; 131 (22): 5671-81.
	Control of embryonic Xenopus morphogenesis by a Ral-GDS/Xral branch of the Ras signalling pathway., Lebreton S., J Cell Sci. November 15, 2003; 116 (Pt 22): 4651-62.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals., Monsoro-Burq AH., Development. July 1, 2003; 130 (14): 3111-24.
	Induction and patterning of the telencephalon in Xenopus laevis., Lupo G., Development. December 1, 2002; 129 (23): 5421-36.
	Role of 14-3-3 proteins in early Xenopus development., Wu C., Mech Dev. November 1, 2002; 119 (1): 45-54.
	SNT-1/FRS2alpha physically interacts with Laloo and mediates mesoderm induction by fibroblast growth factor., Hama J., Mech Dev. December 1, 2001; 109 (2): 195-204.
	Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning., Nutt SL., Genes Dev. May 1, 2001; 15 (9): 1152-66.
	Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis., Ribisi S., Dev Biol. November 1, 2000; 227 (1): 183-96.
	The role of Xenopus dickkopf1 in prechordal plate specification and neural patterning., Kazanskaya O., Development. November 1, 2000; 127 (22): 4981-92.
	FGF signaling and the anterior neural induction in Xenopus., Hongo I., Dev Biol. December 15, 1999; 216 (2): 561-81.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	The Xenopus Ets transcription factor XER81 is a target of the FGF signaling pathway., Münchberg SR., Mech Dev. January 1, 1999; 80 (1): 53-65.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	Mesoderm induction by heterodimeric AP-1 (c-Jun and c-Fos) and its involvement in mesoderm formation through the embryonic fibroblast growth factor/Xbra autocatalytic loop during the early development of Xenopus embryos., Kim J., J Biol Chem. January 16, 1998; 273 (3): 1542-50.
	FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.
	Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus., McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.
	The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins., Latinkić BV., Genes Dev. December 1, 1997; 11 (23): 3265-76.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Expression of Pax-3 is initiated in the early neural plate by posteriorizing signals produced by the organizer and by posterior non-axial mesoderm., Bang AG., Development. May 1, 1997; 124 (10): 2075-85.
	Frzb, a secreted protein expressed in the Spemann organizer, binds and inhibits Wnt-8., Wang S., Cell. March 21, 1997; 88 (6): 757-66.
	Neural induction and patterning in embryos deficient in FGF signaling., Godsave SF., Int J Dev Biol. February 1, 1997; 41 (1): 57-65.
	The Xenopus T-box gene, Antipodean, encodes a vegetally localised maternal mRNA and can trigger mesoderm formation., Stennard F., Development. December 1, 1996; 122 (12): 4179-88.
	Xom: a Xenopus homeobox gene that mediates the early effects of BMP-4., Ladher R., Development. August 1, 1996; 122 (8): 2385-94.
	Factors responsible for the establishment of the body plan in the amphibian embryo., Grunz H., Int J Dev Biol. February 1, 1996; 40 (1): 279-89.
	bFGF as a possible morphogen for the anteroposterior axis of the central nervous system in Xenopus., Kengaku M., Development. September 1, 1995; 121 (9): 3121-30.
	PDGF signalling is required for gastrulation of Xenopus laevis., Ataliotis P., Development. September 1, 1995; 121 (9): 3099-110.
	Induction of the prospective neural crest of Xenopus., Mayor R., Development. March 1, 1995; 121 (3): 767-77.
	The SH2-containing protein-tyrosine phosphatase SH-PTP2 is required upstream of MAP kinase for early Xenopus development., Tang TL., Cell. February 10, 1995; 80 (3): 473-83.
	Regulation of the Xenopus labial homeodomain genes, HoxA1 and HoxD1: activation by retinoids and peptide growth factors., Kolm PJ., Dev Biol. January 1, 1995; 167 (1): 34-49.
	Effect of an inhibitory mutant of the FGF receptor on mesoderm-derived alpha-smooth muscle actin-expressing cells in Xenopus embryo., Saint-Jeannet JP., Dev Biol. August 1, 1994; 164 (2): 374-82.
	Activin-mediated mesoderm induction requires FGF., Cornell RA., Development. February 1, 1994; 120 (2): 453-62.

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