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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.
Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways. , Zhao H ., Development. April 1, 2008; 135 (7): 1283-93.
Retinoic acid-inducible G protein-coupled receptors bind to frizzled receptors and may activate non-canonical Wnt signaling. , Harada Y ., Biochem Biophys Res Commun. July 13, 2007; 358 (4): 968-75.
R-spondin1 is a high affinity ligand for LRP6 and induces LRP6 phosphorylation and beta-catenin signaling. , Wei Q., J Biol Chem. May 25, 2007; 282 (21): 15903-11.
Beta- arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo. , Bryja V ., Proc Natl Acad Sci U S A. April 17, 2007; 104 (16): 6690-5.
Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin. , Kofron M ., Development. February 1, 2007; 134 (3): 503-13.
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.
Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides. , Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
Jun NH2-terminal kinase ( JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos. , Liao G., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.
Maternal XTcf1 and XTcf4 have distinct roles in regulating Wnt target genes. , Standley HJ ., Dev Biol. January 15, 2006; 289 (2): 318-28.
Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation. , Wills A ., Dev Biol. January 1, 2006; 289 (1): 166-78.
Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling. , Swain RK., Cell Commun Signal. October 19, 2005; 3 12.
Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos. , Tao Q , Tao Q ., Cell. March 25, 2005; 120 (6): 857-71.
Exploration of the extracellular space by a large-scale secretion screen in the early Xenopus embryo. , Pera EM ., Int J Dev Biol. January 1, 2005; 49 (7): 781-96.
New roles for FoxH1 in patterning the early embryo. , Kofron M ., Development. October 1, 2004; 131 (20): 5065-78.
XSENP1, a novel sumo-specific protease in Xenopus, inhibits normal head formation by down-regulation of Wnt/beta-catenin signalling. , Yukita A., Genes Cells. August 1, 2004; 9 (8): 723-36.
Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus. , Kuroda H ., PLoS Biol. May 1, 2004; 2 (5): E92.
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.
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.
Regulation of nodal and BMP signaling by tomoregulin-1 ( X7365) through novel mechanisms. , Chang C ., Dev Biol. March 1, 2003; 255 (1): 1-11.
Nodal signaling in Xenopus gastrulae is cell-autonomous and patterned by beta-catenin. , Hashimoto-Partyka MK., Dev Biol. January 1, 2003; 253 (1): 125-38.
The roles of three signaling pathways in the formation and function of the Spemann Organizer. , Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
The IGF pathway regulates head formation by inhibiting Wnt signaling in Xenopus. , Richard-Parpaillon L ., Dev Biol. April 15, 2002; 244 (2): 407-17.
The role of maternal axin in patterning the Xenopus embryo. , Kofron M ., Dev Biol. September 1, 2001; 237 (1): 183-201.
foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain. , Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
FGF signaling restricts the primary blood islands to ventral mesoderm. , Kumano G ., Dev Biol. December 15, 2000; 228 (2): 304-14.
The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner. , Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
Xbra3 induces mesoderm and neural tissue in Xenopus laevis. , Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.
Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach. , Heasman J ., Dev Biol. June 1, 2000; 222 (1): 124-34.
The putative wnt receptor Xenopus frizzled-7 functions upstream of beta-catenin in vertebrate dorsoventral mesoderm patterning. , Sumanas S., Development. May 1, 2000; 127 (9): 1981-90.
Regulation of Wnt signaling by Sox proteins: XSox17 alpha/beta and XSox3 physically interact with beta-catenin. , Zorn AM ., Mol Cell. October 1, 1999; 4 (4): 487-98.
Antagonist activity of DWnt-4 and wingless in the Drosophila embryonic ventral ectoderm and in heterologous Xenopus assays. , Gieseler K ., Mech Dev. July 1, 1999; 85 (1-2): 123-31.
XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development. , Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
derrière: a TGF-beta family member required for posterior development in Xenopus. , Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals. , Pannese M., Mech Dev. April 1, 1998; 73 (1): 73-83.
Blastomere derivation and domains of gene expression in the Spemann Organizer of Xenopus laevis. , Vodicka MA., Development. November 1, 1995; 121 (11): 3505-18.