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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.
Fezf2 promotes neuronal differentiation through localised activation of Wnt/ β-catenin signalling during forebrain development. , Zhang S ., Development. December 1, 2014; 141 (24): 4794-805.
The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning. , Schlosser G ., Dev Biol. May 1, 2014; 389 (1): 98-119.
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.
Early embryonic specification of vertebrate cranial placodes. , Schlosser G ., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis. , Janesick A ., Development. August 1, 2013; 140 (15): 3095-106.
sox4 and sox11 function during Xenopus laevis eye development. , Cizelsky W., PLoS One. July 1, 2013; 8 (7): e69372.
Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene. , Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
Xmab21l3 mediates dorsoventral patterning in Xenopus laevis. , Sridharan J., Mech Dev. July 1, 2012; 129 (5-8): 136-46.
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 RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus. , Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.
Over-expression of atf4 in Xenopus embryos interferes with neurogenesis and eye formation. , Liu JT ., Dongwuxue Yanjiu. October 1, 2011; 32 (5): 485-91.
Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53. , Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.
Xenopus laevis insulin receptor substrate IRS-1 is important for eye development. , Bugner V., Dev Dyn. July 1, 2011; 240 (7): 1705-15.
Peter Pan functions independently of its role in ribosome biogenesis during early eye and craniofacial cartilage development in Xenopus laevis. , Bugner V., Development. June 1, 2011; 138 (11): 2369-78.
Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus. , Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
Histone XH2AX is required for Xenopus anterior neural development: critical role of threonine 16 phosphorylation. , Lee SY., J Biol Chem. September 17, 2010; 285 (38): 29525-34.
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.
Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis. , Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.
Samba, a Xenopus hnRNP expressed in neural and neural crest tissues. , Yan CY., Dev Dyn. January 1, 2009; 238 (1): 204-9.
Evolution of non-coding regulatory sequences involved in the developmental process: reflection of differential employment of paralogous genes as highlighted by Sox2 and group B1 Sox genes. , Kamachi Y., Proc Jpn Acad Ser B Phys Biol Sci. January 1, 2009; 85 (2): 55-68.
Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development. , Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus. , Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.
Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning. , Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.
The lens-regenerating competence in the outer cornea and epidermis of larval Xenopus laevis is related to pax6 expression. , Gargioli C., J Anat. May 1, 2008; 212 (5): 612-20.
PP2A:B56epsilon is required for eye induction and eye field separation. , Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
FoxN3 is required for craniofacial and eye development of Xenopus laevis. , Schuff M., Dev Dyn. January 1, 2007; 236 (1): 226-39.
Expression of Sox1 during Xenopus early embryogenesis. , Nitta KR., Biochem Biophys Res Commun. December 8, 2006; 351 (1): 287-93.
Isolation and characterization of a novel gene, xMADML, involved in Xenopus laevis eye development. , Elkins MB., Dev Dyn. July 1, 2006; 235 (7): 1845-57.
Tes regulates neural crest migration and axial elongation in Xenopus. , Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
A dominant-negative form of the E3 ubiquitin ligase Cullin-1 disrupts the correct allocation of cell fate in the neural crest lineage. , Voigt J., Development. February 1, 2006; 133 (3): 559-68.
Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos. , Reversade B ., Development. August 1, 2005; 132 (15): 3381-92.
Inhibition of neurogenesis by SRp38, a neuroD-regulated RNA-binding protein. , Liu KJ , Liu KJ ., Development. April 1, 2005; 132 (7): 1511-23.
Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays. , Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development. , Takahashi N., Int J Dev Biol. January 1, 2005; 49 (8): 939-51.
A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system. , Saka Y ., Dev Biol. September 15, 2004; 273 (2): 210-25.
Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation. , Leise WF., Development. April 1, 2004; 131 (8): 1703-15.
Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways. , Moore KB ., Dev Cell. January 1, 2004; 6 (1): 55-67.
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.
Depletion of the cell-cycle inhibitor p27( Xic1) impairs neuronal differentiation and increases the number of ElrC(+) progenitor cells in Xenopus tropicalis. , Carruthers S ., Mech Dev. May 1, 2003; 120 (5): 607-16.
Expression of Sox3 throughout the developing central nervous system is dependent on the combined action of discrete, evolutionarily conserved regulatory elements. , Brunelli S., Genesis. May 1, 2003; 36 (1): 12-24.
Characterizing gene expression during lens formation in Xenopus laevis: evaluating the model for embryonic lens induction. , Henry JJ ., Dev Dyn. June 1, 2002; 224 (2): 168-85.
Transcription factors of the anterior neural plate alter cell movements of epidermal progenitors to specify a retinal fate. , Kenyon KL ., Dev Biol. December 1, 2001; 240 (1): 77-91.
XCL-2 is a novel m-type calpain and disrupts morphogenetic movements during embryogenesis in Xenopus laevis. , Cao Y ., Dev Growth Differ. October 1, 2001; 43 (5): 563-71.
Xenopus cadherin-11 restrains cranial neural crest migration and influences neural crest specification. , Borchers A., Development. August 1, 2001; 128 (16): 3049-60.
foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain. , Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
Distinct roles of maf genes during Xenopus lens development. , Ishibashi S ., Mech Dev. March 1, 2001; 101 (1-2): 155-66.
Xenopus Six1 gene is expressed in neurogenic cranial placodes and maintained in the differentiating lateral lines. , Pandur PD ., Mech Dev. September 1, 2000; 96 (2): 253-7.