???pagination.result.count???
???pagination.result.page???
1
ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation. , Wang C ., EMBO Rep. February 1, 2024; 25 (2): 646-671.
Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage. , Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):
Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway. , Ossipova O., Development. September 11, 2020; 147 (17):
Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway. , Ossipova O., Development. January 1, 2020;
A transgenic reporter under control of an es1 promoter/enhancer marks wound epidermis and apical epithelial cap during tail regeneration in Xenopus laevis tadpole. , Sato K ., Dev Biol. January 15, 2018; 433 (2): 404-415.
Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells. , Zhang Z ., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage. , Kirmizitas A., Proc Natl Acad Sci U S A. June 6, 2017; 114 (23): 5814-5821.
The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation. , Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation. , Wills AE ., Dev Cell. February 9, 2015; 32 (3): 345-57.
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.
Lin28 proteins are required for germ layer specification in Xenopus. , Faas L., Development. March 1, 2013; 140 (5): 976-86.
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.
Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1. , Herr P., Development. May 1, 2008; 135 (10): 1813-22.
TGF-beta signaling is required for multiple processes during Xenopus tail regeneration. , Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
Coordination of cell polarity during Xenopus gastrulation. , Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.
Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction. , Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation. , Chang C ., Development. November 1, 2007; 134 (21): 3861-72.
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.
Vg 1 is an essential signaling molecule in Xenopus development. , Birsoy B., Development. January 1, 2006; 133 (1): 15-20.
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.
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.
Lefty blocks a subset of TGFbeta signals by antagonizing EGF- CFC coreceptors. , Cheng SK., PLoS Biol. February 1, 2004; 2 (2): E30.
The nodal target gene Xmenf is a component of an FGF-independent pathway of ventral mesoderm induction in Xenopus. , Kumano G ., Mech Dev. October 1, 2002; 118 (1-2): 45-56.
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.
Beta-catenin, MAPK and Smad signaling during early Xenopus development. , Schohl A ., Development. January 1, 2002; 129 (1): 37-52.
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.
Xenopus Smad3 is specifically expressed in the chordoneural hinge, notochord and in the endocardium of the developing heart. , Howell M., Mech Dev. June 1, 2001; 104 (1-2): 147-50.
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.
Gli2 functions in FGF signaling during antero- posterior patterning. , Brewster R ., Development. October 1, 2000; 127 (20): 4395-405.
Fast1 is required for the development of dorsal axial structures in zebrafish. , Sirotkin HI., Curr Biol. September 7, 2000; 10 (17): 1051-4.
Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif. , Germain S., Genes Dev. February 15, 2000; 14 (4): 435-51.
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.
A mouse homologue of FAST-1 transduces TGF beta superfamily signals and is expressed during early embryogenesis. , Weisberg E., Mech Dev. December 1, 1998; 79 (1-2): 17-27.
Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos. , Bhushan A ., Dev Biol. August 15, 1998; 200 (2): 260-8.
The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities. , Hsu DR., Mol Cell. April 1, 1998; 1 (5): 673-83.