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Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling. , Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.
Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos. , Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.
Rab GTPases are required for early orientation of the left- right axis in Xenopus. , Vandenberg LN., Mech Dev. January 1, 2013; 130 (4-5): 254-71.
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.
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 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.
HEB and E2A function as SMAD/FOXH1 cofactors. , Yoon SJ ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
The RNA-binding protein Xp54nrb isolated from a Ca²+-dependent screen is expressed in neural structures during Xenopus laevis development. , Neant I ., Int J Dev Biol. January 1, 2011; 55 (10-12): 923-31.
Prohibitin1 acts as a neural crest specifier in Xenopus development by repressing the transcription factor E2F1. , Schneider M., Development. December 1, 2010; 137 (23): 4073-81.
Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network. , Yan B ., Dev Dyn. December 1, 2010; 239 (12): 3467-80.
Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin. , Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.
Coordinating the timing of cardiac precursor development during gastrulation: a new role for Notch signaling. , Miazga CM., Dev Biol. September 15, 2009; 333 (2): 285-96.
CDK9/cyclin complexes modulate endoderm induction by direct interaction with Mix.3/ mixer. , Zhu H., Dev Dyn. June 1, 2009; 238 (6): 1346-57.
DeltaNp63 antagonizes p53 to regulate mesoderm induction in Xenopus laevis. , Barton CE., Dev Biol. May 1, 2009; 329 (1): 130-9.
Involvement of an inner nuclear membrane protein, Nemp1, in Xenopus neural development through an interaction with the chromatin protein BAF. , Mamada H., Dev Biol. March 15, 2009; 327 (2): 497-507.
A role for Syndecan-4 in neural induction involving ERK- and PKC-dependent pathways. , Kuriyama S ., Development. February 1, 2009; 136 (4): 575-84.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
Pleiotropic effects in Eya3 knockout mice. , Söker T., BMC Dev Biol. June 23, 2008; 8 118.
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.
The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm. , Spagnoli FM ., Development. February 1, 2008; 135 (3): 451-61.
Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis. , Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.
Hes6 is required for MyoD induction during gastrulation. , Murai K., Dev Biol. December 1, 2007; 312 (1): 61-76.
Xenopus galectin-VIa shows highly specific expression in cement glands and is regulated by canonical Wnt signaling. , Michiue T ., Gene Expr Patterns. October 1, 2007; 7 (8): 852-7.
Wnt/beta-catenin signaling controls Mespo expression to regulate segmentation during Xenopus somitogenesis. , Wang J ., Dev Biol. April 15, 2007; 304 (2): 836-47.
Two oppositely localised frizzled RNAs as axis determinants in a cnidarian embryo. , Momose T., PLoS Biol. April 1, 2007; 5 (4): e70.
The E3 ubiquitin ligase skp2 regulates neural differentiation independent from the cell cycle. , Boix-Perales H., Neural Dev. March 15, 2007; 2 27.
PP2A:B56epsilon is required for eye induction and eye field separation. , Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
Xenopus glucose transporter 1 (xGLUT1) is required for gastrulation movement in Xenopus laevis. , Suzawa K ., Int J Dev Biol. January 1, 2007; 51 (3): 183-90.
Xenopus Dab2 is required for embryonic angiogenesis. , Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
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.
Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis. , Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.
Dystroglycan is required for proper retinal layering. , Lunardi A ., Dev Biol. February 15, 2006; 290 (2): 411-20.
Determination of the minimal domains of Mix.3/ Mixer required for endoderm development. , Doherty JR., Mech Dev. January 1, 2006; 123 (1): 56-66.
Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis. , Shibata M ., Mech Dev. December 1, 2005; 122 (12): 1322-39.
Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus. , Chen JA ., Mech Dev. March 1, 2005; 122 (3): 307-31.
Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation. , Daniels M., Development. November 1, 2004; 131 (22): 5613-26.
The intracellular domain of X- Serrate-1 is cleaved and suppresses primary neurogenesis in Xenopus laevis. , Kiyota T., Mech Dev. June 1, 2004; 121 (6): 573-85.
XIdax, an inhibitor of the canonical Wnt pathway, is required for anterior neural structure formation in Xenopus. , Michiue T ., Dev Dyn. May 1, 2004; 230 (1): 79-90.
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.
Control of embryonic Xenopus morphogenesis by a Ral-GDS/Xral branch of the Ras signalling pathway. , Lebreton S., J Cell Sci. November 15, 2003; 116 (Pt 22): 4651-62.
Dlx proteins position the neural plate border and determine adjacent cell fates. , Woda JM., Development. January 1, 2003; 130 (2): 331-42.
A single cdk inhibitor, p27Xic1, functions beyond cell cycle regulation to promote muscle differentiation in Xenopus. , Vernon AE., Development. January 1, 2003; 130 (1): 71-83.
The Xenopus receptor tyrosine kinase Xror2 modulates morphogenetic movements of the axial mesoderm and neuroectoderm via Wnt signaling. , Hikasa H., Development. November 1, 2002; 129 (22): 5227-39.
Effects of heterodimerization and proteolytic processing on Derrière and Nodal activity: implications for mesoderm induction in Xenopus. , Eimon PM., Development. July 1, 2002; 129 (13): 3089-103.
Smad10 is required for formation of the frog nervous system. , LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
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.
SNT-1/ FRS2alpha physically interacts with Laloo and mediates mesoderm induction by fibroblast growth factor. , Hama J., Mech Dev. December 1, 2001; 109 (2): 195-204.
Proteolytic cleavage of Chordin as a switch for the dual activities of Twisted gastrulation in BMP signaling. , Larraín J ., Development. November 1, 2001; 128 (22): 4439-47.
Expression of activated MAP kinase in Xenopus laevis embryos: evaluating the roles of FGF and other signaling pathways in early induction and patterning. , Curran KL ., Dev Biol. December 1, 2000; 228 (1): 41-56.