Papers associated with tail bud (and fgf2)

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	Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):
	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;
	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.
	Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
	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.
	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.
	Temporal and spatial expression of FGF ligands and receptors during Xenopus development., Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.
	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.
	Formation of the ascidian epidermal sensory neurons: insights into the origin of the chordate peripheral nervous system., Pasini A., PLoS Biol. July 1, 2006; 4 (7): e225.
	BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.
	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.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	Using Xenopus as a model system for an undergraduate laboratory course in vertebrate development at the University of Bordeaux, France., Olive M., Int J Dev Biol. January 1, 2003; 47 (2-3): 153-60.
	Common and distinct signals specify the distribution of blood and vascular cell lineages in Xenopus laevis embryos., Iraha F., Dev Growth Differ. October 1, 2002; 44 (5): 395-407.
	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.
	Phosphatidylinositol-3 kinase acts in parallel to the ERK MAP kinase in the FGF pathway during Xenopus mesoderm induction., Carballada R., Development. January 1, 2001; 128 (1): 35-44.
	Participation of transcription elongation factor XSII-K1 in mesoderm-derived tissue development in Xenopus laevis., Taira Y., J Biol Chem. October 13, 2000; 275 (41): 32011-5.
	Expression pattern of BXR suggests a role for benzoate ligand-mediated signalling in hatching gland function., Heath LA., Int J Dev Biol. January 1, 2000; 44 (1): 141-4.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	SCL specifies hematopoietic mesoderm in Xenopus embryos., Mead PE., Development. July 1, 1998; 125 (14): 2611-20.
	Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins., Sparrow DB., Mech Dev. February 1, 1998; 71 (1-2): 151-63.
	FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.
	Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development., Heller N., Mech Dev. December 1, 1997; 69 (1-2): 83-104.
	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.
	A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis., Chang C., Development. February 1, 1997; 124 (4): 827-37.
	Xom: a Xenopus homeobox gene that mediates the early effects of BMP-4., Ladher R., Development. August 1, 1996; 122 (8): 2385-94.
	A novel MAP kinase phosphatase is localised in the branchial arch region and tail tip of Xenopus embryos and is inducible by retinoic acid., Mason C., Mech Dev. April 1, 1996; 55 (2): 133-44.
	Early regionalized expression of a novel Xenopus fibroblast growth factor receptor in neuroepithelium., Riou JF., Biochem Biophys Res Commun. January 5, 1996; 218 (1): 198-204.
	Caudalization of neural fate by tissue recombination and bFGF., Cox WG., Development. December 1, 1995; 121 (12): 4349-58.
	The identification of two novel ligands of the FGF receptor by a yeast screening method and their activity in Xenopus development., Kinoshita N., Cell. November 17, 1995; 83 (4): 621-30.
	Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern., Lamb TM., Development. November 1, 1995; 121 (11): 3627-36.
	Developmental and differential regulations in gene expression of Xenopus pleiotrophic factors-alpha and -beta., Tsujimura A., Biochem Biophys Res Commun. September 14, 1995; 214 (2): 432-9.
	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.
	Spatial and temporal expression of basic fibroblast growth factor (FGF-2) mRNA and protein in early Xenopus development., Song J., Mech Dev. December 1, 1994; 48 (3): 141-51.
	Induction of cardiac muscle differentiation in isolated animal pole explants of Xenopus laevis embryos., Logan M., Development. July 1, 1993; 118 (3): 865-75.
	[Regionalization of the expression of tenascin as a response to the inducers of mesoderm]., Umbhauer M., C R Seances Soc Biol Fil. January 1, 1993; 187 (3): 341-55.
	Pintallavis, a gene expressed in the organizer and midline cells of frog embryos: involvement in the development of the neural axis., Ruiz i Altaba A., Development. September 1, 1992; 116 (1): 81-93.
	Developmental expression of the Xenopus int-2 (FGF-3) gene: activation by mesodermal and neural induction., Tannahill D., Development. July 1, 1992; 115 (3): 695-702.
	Xenopus blastulae show regional differences in competence for mesoderm induction: correlation with endogenous basic fibroblast growth factor levels., Godsave SF., Dev Biol. June 1, 1992; 151 (2): 506-15.
	Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification., Isaacs HV., Development. March 1, 1992; 114 (3): 711-20.
	Specification of the body plan during Xenopus gastrulation: dorsoventral and anteroposterior patterning of the mesoderm., Slack JM., Dev Suppl. January 1, 1992; 143-9.
	Localized and inducible expression of Xenopus-posterior (Xpo), a novel gene active in early frog embryos, encoding a protein with a ''CCHC'' finger domain., Sato SM., Development. July 1, 1991; 112 (3): 747-53.

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