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Maternal Huluwa dictates the embryonic body axis through β-catenin in vertebrates. , Yan L., Science. November 23, 2018; 362 (6417):
Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula. , Ding Y ., Dev Biol. June 15, 2017; 426 (2): 176-187.
Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing. , Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.
A gradient of maternal Bicaudal-C controls vertebrate embryogenesis via translational repression of mRNAs encoding cell fate regulators. , Park S., Development. March 1, 2016; 143 (5): 864-71.
Specification of anteroposterior axis by combinatorial signaling during Xenopus development. , Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
NF2/ Merlin is required for the axial pattern formation in the Xenopus laevis embryo. , Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.
Sulf1 has ligand-dependent effects on canonical and non-canonical Wnt signalling. , Fellgett SW., J Cell Sci. April 1, 2015; 128 (7): 1408-21.
Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo. , Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling. , Zhang Y ., Dev Biol. August 1, 2014; 392 (1): 15-25.
Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus. , Colozza G ., Differentiation. July 1, 2014; 88 (1): 17-26.
Left- right asymmetry: lessons from Cancún. , Burdine RD., Development. November 1, 2013; 140 (22): 4465-70.
Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification. , Mei W., Development. June 1, 2013; 140 (11): 2334-44.
Maternal Mga is required for Wnt signaling and organizer formation in the early Xenopus embryo. , Gu F., Acta Biochim Biophys Sin (Shanghai). November 1, 2012; 44 (11): 939-47.
Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation. , Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/ β-catenin signaling pathway. , Fujimi TJ ., Dev Biol. January 15, 2012; 361 (2): 220-31.
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.
The functions of maternal Dishevelled 2 and 3 in the early Xenopus embryo. , Tadjuidje E ., Dev Dyn. July 1, 2011; 240 (7): 1727-36.
Yes-associated protein 65 ( YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone. , Gee ST ., PLoS One. January 1, 2011; 6 (6): e20309.
Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo. , Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2. , Blythe SA ., Dev Cell. August 17, 2010; 19 (2): 220-31.
Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling. , Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
Vegetally localized Xenopus trim36 regulates cortical rotation and dorsal axis formation. , Cuykendall TN ., Development. September 1, 2009; 136 (18): 3057-65.
Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1. , Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
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.
Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6. , Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.
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.
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.
Distinct PAR-1 proteins function in different branches of Wnt signaling during vertebrate development. , Ossipova O., Dev Cell. June 1, 2005; 8 (6): 829-41.
XIC is required for Siamois activity and dorsoanterior development. , Snider L ., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
New roles for FoxH1 in patterning the early embryo. , Kofron M ., Development. October 1, 2004; 131 (20): 5065-78.
The involvement of Frodo in TCF-dependent signaling and neural tissue development. , Hikasa H., Development. October 1, 2004; 131 (19): 4725-34.
Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays. , Wessely O ., Dev Biol. May 15, 2004; 269 (2): 552-66.
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.
A novel role for a nodal-related protein; Xnr3 regulates convergent extension movements via the FGF receptor. , Yokota C., Development. May 1, 2003; 130 (10): 2199-212.
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.
Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus. , Wessely O ., Dev Biol. June 1, 2001; 234 (1): 161-73.
[Neural determination in Xenopus laevis embryos: control of early neural gene expression by calcium]. , Leclerc C ., J Soc Biol. January 1, 2001; 195 (3): 327-37.
FGF signaling restricts the primary blood islands to ventral mesoderm. , Kumano G ., Dev Biol. December 15, 2000; 228 (2): 304-14.
The Toll/ IL-1 receptor binding protein MyD88 is required for Xenopus axis formation. , Prothmann C., Mech Dev. October 1, 2000; 97 (1-2): 85-92.
Regulation of early expression of Dlx3, a Xenopus anti-neural factor, by beta-catenin signaling. , Beanan MJ., Mech Dev. March 1, 2000; 91 (1-2): 227-35.
Endodermal Nodal-related signals and mesoderm induction in Xenopus. , Agius E ., Development. March 1, 2000; 127 (6): 1173-83.
Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development. , Baker JC ., Genes Dev. December 1, 1999; 13 (23): 3149-59.
A cell-free assay system for beta-catenin signaling that recapitulates direct inductive events in the early xenopus laevis embryo. , Nelson RW ., J Cell Biol. October 18, 1999; 147 (2): 367-74.
Amphibian embryos as a model system for organ engineering: in vitro induction and rescue of the heart anlage. , Grunz H ., Int J Dev Biol. July 1, 1999; 43 (4): 361-4.
Rearranging gastrulation in the name of yolk: evolution of gastrulation in yolk-rich amniote eggs. , Arendt D ., Mech Dev. March 1, 1999; 81 (1-2): 3-22.
Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis. , Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.