Papers associated with regenerating tail (and odc1)

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	Noggin4 is a long-range inhibitor of Wnt8 signalling that regulates head development in Xenopus laevis., Eroshkin FM., Sci Rep. January 22, 2016; 6 23049.
	Expression pattern of bcar3, a downstream target of Gata2, and its binding partner, bcar1, during Xenopus development., Green YS., Gene Expr Patterns. January 1, 2016; 20 (1): 55-62.
	Huntingtin is required for ciliogenesis and neurogenesis during early Xenopus development., Haremaki T., Dev Biol. December 15, 2015; 408 (2): 305-15.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	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.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo., Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
	The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	High-resolution analysis of gene activity during the Xenopus mid-blastula transition., Collart C., Development. May 1, 2014; 141 (9): 1927-39.
	An essential role for LPA signalling in telencephalon development., Geach TJ., Development. February 1, 2014; 141 (4): 940-9.
	Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
	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.
	β-Adrenergic signaling promotes posteriorization in Xenopus early development., Mori S., Dev Growth Differ. April 1, 2013; 55 (3): 350-8.
	Agr genes, missing in amniotes, are involved in the body appendages regeneration in frog tadpoles., Ivanova AS., Sci Rep. January 1, 2013; 3 1279.
	fus/TLS orchestrates splicing of developmental regulators during gastrulation., Dichmann DS., Genes Dev. June 15, 2012; 26 (12): 1351-63.
	Homeoprotein hhex-induced conversion of intestinal to ventral pancreatic precursors results in the formation of giant pancreata in Xenopus embryos., Zhao H., Proc Natl Acad Sci U S A. May 29, 2012; 109 (22): 8594-9.
	Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae., Rodrigues AM., BMC Dev Biol. February 27, 2012; 12 9.
	Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney., Sauert K., PLoS One. January 1, 2012; 7 (3): e33522.
	xCITED2 Induces Neural Genes in Animal Cap Explants of Xenopus Embryos., Yoon J., Exp Neurobiol. September 1, 2011; 20 (3): 123-9.
	Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos., Canning CA., Dev Dyn. August 1, 2011; 240 (8): 1958-63.
	Appl1 is essential for the survival of Xenopus pancreas, duodenum, and stomach progenitor cells., Wen L., Dev Dyn. August 1, 2010; 239 (8): 2198-207.
	Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin., Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.
	The RNA-binding protein Seb4/RBM24 is a direct target of MyoD and is required for myogenesis during Xenopus early development., Li HY., Mech Dev. January 1, 2010; 127 (5-6): 281-91.
	The lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) receptor gene families: cloning and comparative expression analysis in Xenopus laevis., Massé K., Int J Dev Biol. January 1, 2010; 54 (8-9): 1361-74.
	Xenopus Rnd1 and Rnd3 GTP-binding proteins are expressed under the control of segmentation clock and required for somite formation., Goda T., Dev Dyn. November 1, 2009; 238 (11): 2867-76.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.
	Activin/nodal signaling modulates XPAPC expression during Xenopus gastrulation., Lou X., Dev Dyn. March 1, 2008; 237 (3): 683-91.
	Expression analysis of IGFBP-rP10, IGFBP-like and Mig30 in early Xenopus development., Kuerner KM., Dev Dyn. October 1, 2006; 235 (10): 2861-7.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	A consensus Oct1 binding site is required for the activity of the Xenopus Cdx4 promoter., Reece-Hoyes JS., Dev Biol. June 15, 2005; 282 (2): 509-23.
	Expression of Xenopus XlSALL4 during limb development and regeneration., Neff AW., Dev Dyn. June 1, 2005; 233 (2): 356-67.
	Notch signaling modulates the nuclear localization of carboxy-terminal-phosphorylated smad2 and controls the competence of ectodermal cells for activin A., Abe T., Mech Dev. May 1, 2005; 122 (5): 671-80.
	XEpac, a guanine nucleotide-exchange factor for Rap GTPase, is a novel hatching gland specific marker during the Xenopus embryogenesis., Lee SJ., Dev Dyn. April 1, 2005; 232 (4): 1091-7.
	JNK and ROKalpha function in the noncanonical Wnt/RhoA signaling pathway to regulate Xenopus convergent extension movements., Kim GH., Dev Dyn. April 1, 2005; 232 (4): 958-68.
	BMP4-dependent expression of Xenopus Grainyhead-like 1 is essential for epidermal differentiation., Tao J., Development. March 1, 2005; 132 (5): 1021-34.
	Developmental expression of Pod 1 in Xenopus laevis., Simrick S., Int J Dev Biol. January 1, 2005; 49 (1): 59-63.
	Identification of Xenopus cyclin-dependent kinase inhibitors, p16Xic2 and p17Xic3., Daniels M., Gene. November 10, 2004; 342 (1): 41-7.
	The POU factor Oct-25 regulates the Xvent-2B gene and counteracts terminal differentiation in Xenopus embryos., Cao Y, Cao Y., J Biol Chem. October 15, 2004; 279 (42): 43735-43.
	Xenopus tropicalis nodal-related gene 3 regulates BMP signaling: an essential role for the pro-region., Haramoto Y., Dev Biol. January 1, 2004; 265 (1): 155-68.
	Identification and characterization of Xenopus NDRG1., Kyuno J., Biochem Biophys Res Commun. September 12, 2003; 309 (1): 52-7.
	A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I., Mol Cell. August 1, 2003; 12 (2): 425-35.
	Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.
	The prickle-related gene in vertebrates is essential for gastrulation cell movements., Takeuchi M., Curr Biol. April 15, 2003; 13 (8): 674-9.
	Characterization of the Xenopus galectin family. Three structurally different types as in mammals and regulated expression during embryogenesis., Shoji H., J Biol Chem. April 4, 2003; 278 (14): 12285-93.
	The latent-TGFbeta-binding-protein-1 (LTBP-1) is expressed in the organizer and regulates nodal and activin signaling., Altmann CR., Dev Biol. August 1, 2002; 248 (1): 118-27.

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