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Mechanical Tensions Regulate Gene Expression in the Xenopus laevis Axial Tissues. , Eroshkin FM., Int J Mol Sci. January 10, 2024; 25 (2):
Rspo2 inhibits TCF3 phosphorylation to antagonize Wnt signaling during vertebrate anteroposterior axis specification. , Reis AH., Sci Rep. June 28, 2021; 11 (1): 13433.
Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos. , Lichtig H., Front Physiol. January 1, 2020; 11 75.
Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus. , Gentsch GE ., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.
Two-Element Transcriptional Regulation in the Canonical Wnt Pathway. , Kim K., Curr Biol. August 7, 2017; 27 (15): 2357-2364.e5.
Genomic integration of Wnt/ β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs. , Stevens ML ., Development. April 1, 2017; 144 (7): 1283-1295.
FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue. , Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
Tissue- and stage-specific Wnt target gene expression is controlled subsequent to β-catenin recruitment to cis-regulatory modules. , Nakamura Y., Development. June 1, 2016; 143 (11): 1914-25.
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.
Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites. , Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y ., Development. October 1, 2014; 141 (19): 3740-51.
Molecular insights into the origin of the Hox-TALE patterning system. , Hudry B., Elife. March 18, 2014; 3 e01939.
An essential role for LPA signalling in telencephalon development. , Geach TJ ., Development. February 1, 2014; 141 (4): 940-9.
Left- right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions. , Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning. , Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
MRAS GTPase is a novel stemness marker that impacts mouse embryonic stem cell plasticity and Xenopus embryonic cell fate. , Mathieu ME., Development. August 1, 2013; 140 (16): 3311-22.
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.
Identification and characterization of Xenopus kctd15, an ectodermal gene repressed by the FGF pathway. , Takahashi C ., Int J Dev Biol. January 1, 2012; 56 (5): 393-402.
XMeis3 is necessary for mesodermal Hox gene expression and function. , In der Rieden PM ., PLoS One. March 9, 2011; 6 (3): e18010.
SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos. , Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
Regulation of TCF3 by Wnt-dependent phosphorylation during vertebrate axis specification. , Hikasa H., Dev Cell. October 19, 2010; 19 (4): 521-32.
Xwnt8 directly initiates expression of labial Hox genes. , In der Rieden PM ., Dev Dyn. January 1, 2010; 239 (1): 126-39.
Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation. , Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.
Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function. , Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.
The RNA-binding protein Mex3b has a fine-tuning system for mRNA regulation in early Xenopus development. , Takada H., Development. July 1, 2009; 136 (14): 2413-22.
Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis. , Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.
Characterisation of the fibroblast growth factor dependent transcriptome in early development. , Branney PA., PLoS One. January 1, 2009; 4 (3): e4951.
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development. , Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
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.
Microarray-based identification of VegT targets in Xenopus. , Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.
Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition. , Delaune E., Development. January 1, 2005; 132 (2): 299-310.
Integration of multiple signal transducing pathways on Fgf response elements of the Xenopus caudal homologue Xcad3. , Haremaki T ., Development. October 1, 2003; 130 (20): 4907-17.
Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth. , Beck CW ., Mech Dev. March 1, 1998; 72 (1-2): 41-52.
Dorsal- ventral differences in Xcad-3 expression in response to FGF-mediated induction in Xenopus. , Northrop JL., Dev Biol. February 1, 1994; 161 (2): 490-503.