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Global analysis of gene expression in Xenopus hindlimbs during stage-dependent complete and incomplete regeneration. , Grow M ., Dev Dyn. October 1, 2006; 235 (10): 2667-85.
Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination. , Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.
Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles. , Beck CW ., Mech Dev. September 1, 2006; 123 (9): 674-88.
FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development. , Urban AE ., Dev Biol. September 1, 2006; 297 (1): 103-17.
Xenopus Xotx2 and Drosophila otd share similar activities in anterior patterning of the frog embryo. , Lunardi A ., Dev Genes Evol. September 1, 2006; 216 (9): 511-21.
Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity. , Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development. , Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus. , Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
Tes regulates neural crest migration and axial elongation in Xenopus. , Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
FGF8, Wnt8 and Myf5 are target genes of Tbx6 during anteroposterior specification in Xenopus embryo. , Li HY., Dev Biol. February 15, 2006; 290 (2): 470-81.
Ras-dva, a member of novel family of small GTPases, is required for the anterior ectoderm patterning in the Xenopus laevis embryo. , Tereshina MB., Development. February 1, 2006; 133 (3): 485-94.
The zic1 gene is an activator of Wnt signaling. , Merzdorf CS ., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis. , Ahrens K ., Dev Biol. December 1, 2005; 288 (1): 40-59.
Nerve-dependent and -independent events in blastema formation during Xenopus froglet limb regeneration. , Suzuki M ., Dev Biol. October 1, 2005; 286 (1): 361-75.
The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system. , Huang X ., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.
Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos. , Reversade B ., Development. August 1, 2005; 132 (15): 3381-92.
Dorsoventral patterning of the Xenopus eye: a collaboration of Retinoid, Hedgehog and FGF receptor signaling. , Lupo G., Development. April 1, 2005; 132 (7): 1737-48.
Regulated expression pattern of gremlin during zebrafish development. , Nicoli S., Gene Expr Patterns. April 1, 2005; 5 (4): 539-44.
XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis. , Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.
Conserved cross-interactions in Drosophila and Xenopus between Ras/ MAPK signaling and the dual-specificity phosphatase MKP3. , Gómez AR., Dev Dyn. March 1, 2005; 232 (3): 695-708.
Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction. , Monsoro-Burq AH ., Dev Cell. February 1, 2005; 8 (2): 167-78.
XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development. , Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
Insulin-like growth factor (IGF) signalling is required for early dorso- anterior development of the zebrafish embryo. , Eivers E., Int J Dev Biol. December 1, 2004; 48 (10): 1131-40.
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.
R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis. , Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
New roles for FoxH1 in patterning the early embryo. , Kofron M ., Development. October 1, 2004; 131 (20): 5065-78.
Pbx genes are required in Xenopus lens development. , Morgan R., Int J Dev Biol. September 1, 2004; 48 (7): 623-7.
Expression patterns of Xenopus FGF receptor-like 1/ nou-darake in early Xenopus development resemble those of planarian nou-darake and Xenopus FGF8. , Hayashi S., Dev Dyn. August 1, 2004; 230 (4): 700-7.
Regulation of Otx2 expression and its functions in mouse epiblast and anterior neuroectoderm. , Kurokawa D., Development. July 1, 2004; 131 (14): 3307-17.
Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation. , Shiotsugu J., Development. June 1, 2004; 131 (11): 2653-67.
Evolutionarily conserved expression pattern and trans-regulating activity of Xenopus p51/ p63. , Tomimori Y., Biochem Biophys Res Commun. January 9, 2004; 313 (2): 230-6.
PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development. , Yang J ., Development. December 1, 2003; 130 (23): 5569-78.
Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos. , Galli A., Development. October 1, 2003; 130 (20): 4919-29.
Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor. , Bell E ., Development. April 1, 2003; 130 (7): 1381-9.
Induction and patterning of the telencephalon in Xenopus laevis. , Lupo G., Development. December 1, 2002; 129 (23): 5421-36.
Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud. , Aoto K., Dev Biol. November 15, 2002; 251 (2): 320-32.
Isthmin is a novel secreted protein expressed as part of the Fgf-8 synexpression group in the Xenopus midbrain- hindbrain organizer. , Pera EM ., Mech Dev. August 1, 2002; 116 (1-2): 169-72.
The role of the anterior neural ridge and Fgf-8 in early forebrain patterning and regionalization in Xenopus laevis. , Eagleson GW ., Comp Biochem Physiol B Biochem Mol Biol. May 1, 2002; 132 (1): 179-89.
The homeoprotein Xiro1 is required for midbrain- hindbrain boundary formation. , Glavic A ., Development. April 1, 2002; 129 (7): 1609-21.
Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo. , Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.
The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling. , Domingos PM ., Dev Biol. November 1, 2001; 239 (1): 148-60.
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.
Foregut endoderm is required at head process stages for anteriormost neural patterning in chick. , Withington S., Development. February 1, 2001; 128 (3): 309-20.
An epidermal signal regulates Lmx-1 expression and dorsal- ventral pattern during Xenopus limb regeneration. , Matsuda H., Dev Biol. January 15, 2001; 229 (2): 351-62.
Cloning, expression and nuclear localization of human NPM3, a member of the nucleophosmin/ nucleoplasmin family of nuclear chaperones. , Shackleford GM., BMC Genomics. January 1, 2001; 2 8.
Expression patterns of Fgf-8 during development and limb regeneration of the axolotl. , Han MJ., Dev Dyn. January 1, 2001; 220 (1): 40-8.
Mechanisms of left- right determination in vertebrates. , Capdevila J., Cell. March 31, 2000; 101 (1): 9-21.
Induction and differentiation of the zebrafish heart requires fibroblast growth factor 8 ( fgf8/acerebellar). , Reifers F., Development. January 1, 2000; 127 (2): 225-35.
The midbrain- hindbrain boundary genetic cascade is activated ectopically in the diencephalon in response to the widespread expression of one of its components, the medaka gene Ol- eng2. , Ristoratore F., Development. September 1, 1999; 126 (17): 3769-79.
Gli3 is required for Emx gene expression during dorsal telencephalon development. , Theil T., Development. August 1, 1999; 126 (16): 3561-71.