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Pou5f3.2-induced proliferative state of embryonic cells during gastrulation of Xenopus laevis embryo. , Nishitani E., Dev Growth Differ. December 1, 2015; 57 (9): 591-600.
Efficient retina formation requires suppression of both Activin and BMP signaling pathways in pluripotent cells. , Wong KA., Biol Open. March 6, 2015; 4 (4): 573-83.
Genome-wide view of TGFβ/ Foxh1 regulation of the early mesendoderm program. , Chiu WT ., Development. December 1, 2014; 141 (23): 4537-47.
Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm. , Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
A potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome. , Tanaka K., Dev Biol. March 1, 2014; 387 (1): 28-36.
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.
Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling. , Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.
RAB8B is required for activity and caveolar endocytosis of LRP6. , Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.
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.
TBX3 Directs Cell-Fate Decision toward Mesendoderm. , Weidgang CE., Stem Cell Reports. August 29, 2013; 1 (3): 248-65.
Brain-specific promoter/exon I.f of the cyp19a1 ( aromatase) gene in Xenopus laevis. , Nakagawa T., J Steroid Biochem Mol Biol. November 1, 2012; 132 (3-5): 247-55.
Conservation and evolutionary divergence in the activity of receptor-regulated smads. , Sorrentino GM ., Evodevo. October 1, 2012; 3 (1): 22.
Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins. , Callery EM ., Open Biol. April 1, 2012; 2 (4): 120060.
mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/ nodal signaling in Xenopus ectodermal cells. , Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos. , Lee SY., Differentiation. September 1, 2011; 82 (2): 99-107.
The role and regulation of GDF11 in Smad2 activation during tailbud formation in the Xenopus embryo. , Ho DM., Mech Dev. January 1, 2010; 127 (9-12): 485-95.
Identification of a novel negative regulator of activin/ nodal signaling in mesendodermal formation of Xenopus embryos. , Cheong SM., J Biol Chem. June 19, 2009; 284 (25): 17052-60.
Oct25 represses transcription of nodal/activin target genes by interaction with signal transducers during Xenopus gastrulation. , Cao Y ., J Biol Chem. December 5, 2008; 283 (49): 34168-77.
Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation. , Cha SW ., Development. November 1, 2008; 135 (22): 3719-29.
Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1. , Herr P., Development. May 1, 2008; 135 (10): 1813-22.
Coordination of cell polarity during Xenopus gastrulation. , Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.
The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm. , Spagnoli FM ., Development. February 1, 2008; 135 (3): 451-61.
Tsukushi modulates Xnr2, FGF and BMP signaling: regulation of Xenopus germ layer formation. , Morris SA., PLoS One. October 10, 2007; 2 (10): e1004.
Tpt1 activates transcription of oct4 and nanog in transplanted somatic nuclei. , Koziol MJ., Curr Biol. May 1, 2007; 17 (9): 801-7.
Negative regulation of Activin/ Nodal signaling by SRF during Xenopus gastrulation. , Yun CH., Development. February 1, 2007; 134 (4): 769-77.
Xenopus Dab2 is required for embryonic angiogenesis. , Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development. , Steiner AB., Development. December 1, 2006; 133 (24): 4827-38.
GDF3, a BMP inhibitor, regulates cell fate in stem cells and early embryos. , Levine AJ., Development. January 1, 2006; 133 (2): 209-16.
Vg 1 is an essential signaling molecule in Xenopus development. , Birsoy B., Development. January 1, 2006; 133 (1): 15-20.
The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo. , Collart C ., Development. October 1, 2005; 132 (20): 4575-86.
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.
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.
Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase. , Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
Functional specificity of the Xenopus T-domain protein Brachyury is conferred by its ability to interact with Smad1. , Messenger NJ., Dev Cell. April 1, 2005; 8 (4): 599-610.
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.
Conditional BMP inhibition in Xenopus reveals stage-specific roles for BMPs in neural and neural crest induction. , Wawersik S., Dev Biol. January 15, 2005; 277 (2): 425-42.
Visualizing long-range movement of the morphogen Xnr2 in the Xenopus embryo. , Williams PH., Curr Biol. November 9, 2004; 14 (21): 1916-23.
Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation. , Daniels M., Development. November 1, 2004; 131 (22): 5613-26.
New roles for FoxH1 in patterning the early embryo. , Kofron M ., Development. October 1, 2004; 131 (20): 5065-78.
Nodal-dependent Cripto signaling promotes cardiomyogenesis and redirects the neural fate of embryonic stem cells. , Parisi S., J Cell Biol. October 27, 2003; 163 (2): 303-14.
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.
Action range of BMP is defined by its N-terminal basic amino acid core. , Ohkawara B., Curr Biol. February 5, 2002; 12 (3): 205-9.
Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis. , Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
Timing of endogenous activin-like signals and regional specification of the Xenopus embryo. , Lee MA., Development. August 1, 2001; 128 (15): 2939-52.
Mesendoderm induction and reversal of left- right pattern by mouse Gdf1, a Vg1-related gene. , Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.
Expression regulation of hyaluronan synthase in corneal endothelial cells. , Usui T., Invest Ophthalmol Vis Sci. October 1, 2000; 41 (11): 3261-7.
Gli2 functions in FGF signaling during antero- posterior patterning. , Brewster R ., Development. October 1, 2000; 127 (20): 4395-405.
Cloning and characterization of zebrafish smad2, smad3 and smad4. , Dick A., Gene. April 4, 2000; 246 (1-2): 69-80.
Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4. , Nishinakamura R., Dev Biol. December 15, 1999; 216 (2): 481-90.