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Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration. , Patel JH., Dev Biol. March 1, 2022; 483 157-168.
Wnt-inducible Lrp6- APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway. , Colozza G ., Sci Rep. December 9, 2020; 10 (1): 21555.
Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo. , Gouignard N ., PLoS One. January 18, 2018; 13 (1): e0191751.
An atlas of Wnt activity during embryogenesis in Xenopus tropicalis. , Borday C., PLoS One. January 1, 2018; 13 (4): e0193606.
Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover. , Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/ β-catenin signaling and are essential for head formation in Xenopus. , Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.
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.
Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling. , Sheng R., Nat Commun. July 15, 2014; 5 4393.
Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus. , Young JJ ., Development. April 1, 2014; 141 (8): 1683-93.
The Prdm13 histone methyltransferase encoding gene is a Ptf1a- Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube. , Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.
An essential role for LPA signalling in telencephalon development. , Geach TJ ., Development. February 1, 2014; 141 (4): 940-9.
Role of Sp5 as an essential early regulator of neural crest specification in xenopus. , Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.
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.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development. , Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.
The forkhead transcription factor FoxB1 regulates the dorsal- ventral and anterior- posterior patterning of the ectoderm during early Xenopus embryogenesis. , Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.
The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo. , Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2. , Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
FMR1/ FXR1 and the miRNA pathway are required for eye and neural crest development. , Gessert S., Dev Biol. May 1, 2010; 341 (1): 222-35.
The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos. , Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
The lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) receptor gene families: cloning and comparative expression analysis in Xenopus laevis. , Massé K ., Int J Dev Biol. January 1, 2010; 54 (8-9): 1361-74.
Vestigial like gene family expression in Xenopus: common and divergent features with other vertebrates. , Faucheux C., Int J Dev Biol. January 1, 2010; 54 (8-9): 1375-82.
Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus. , Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
Zebrafish gbx1 refines the midbrain- hindbrain boundary border and mediates the Wnt8 posteriorization signal. , Rhinn M., Neural Dev. April 2, 2009; 4 12.
Complementary expression of HSPG 6-O-endosulfatases and 6-O-sulfotransferase in the hindbrain of Xenopus laevis. , Winterbottom EF., Gene Expr Patterns. March 1, 2009; 9 (3): 166-72.
Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation. , Inomata H ., Cell. September 5, 2008; 134 (5): 854-65.
VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development. , Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.
Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation. , Chang C ., Development. November 1, 2007; 134 (21): 3861-72.
The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo. , Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
The homeodomain factor Xanf represses expression of genes in the presumptive rostral forebrain that specify more caudal brain regions. , Ermakova GV., Dev Biol. July 15, 2007; 307 (2): 483-97.
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo- mesoderm promoting pathways. , Yan B ., Dev Biol. May 1, 2007; 305 (1): 103-19.
Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/ Smad1 pathway. , Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.
Neural induction in Xenopus requires inhibition of Wnt-beta-catenin signaling. , Heeg-Truesdell E., Dev Biol. October 1, 2006; 298 (1): 71-86.
Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis. , Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.
Combined ectopic expression of Pdx1 and Ptf1a/p48 results in the stable conversion of posterior endoderm into endocrine and exocrine pancreatic tissue. , Afelik S., Genes Dev. June 1, 2006; 20 (11): 1441-6.
XNF-ATc3 affects neural convergent extension. , Borchers A ., Development. May 1, 2006; 133 (9): 1745-55.
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.
Regulation of early Xenopus development by ErbB signaling. , Nie S ., Dev Dyn. February 1, 2006; 235 (2): 301-14.
The zic1 gene is an activator of Wnt signaling. , Merzdorf CS ., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field. , Reversade B ., Cell. December 16, 2005; 123 (6): 1147-60.
Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer. , Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.
Cloning and characterisation of the immunophilin X- CypA in Xenopus laevis. , Massé K ., Gene Expr Patterns. November 1, 2004; 5 (1): 51-60.
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.
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.
Wise, a context-dependent activator and inhibitor of Wnt signalling. , Itasaki N., Development. September 1, 2003; 130 (18): 4295-305.
Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway. , Zhao H ., Dev Biol. May 15, 2003; 257 (2): 278-91.