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Regulation of gene expression downstream of a novel Fgf/Erk pathway during Xenopus development. , Cowell LM., PLoS One. January 1, 2023; 18 (10): e0286040.
Goosecoid Controls Neuroectoderm Specification via Dual Circuits of Direct Repression and Indirect Stimulation in Xenopus Embryos. , Umair Z., Mol Cells. October 31, 2021; 44 (10): 723-735.
The cytokine FAM3B/PANDER is an FGFR ligand that promotes posterior development in Xenopus. , Zhang F., Proc Natl Acad Sci U S A. May 18, 2021; 118 (20):
Dusp1 modulates activin/smad2 mediated germ layer specification via FGF signal inhibition in Xenopus embryos. , Umair Z., Anim Cells Syst (Seoul). November 27, 2020; 24 (6): 359-370.
What are the roles of retinoids, other morphogens, and Hox genes in setting up the vertebrate body axis? , Durston AJ ., Genesis. July 1, 2019; 57 (7-8): e23296.
Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis. , Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.
Coordinated regulation of the dorsal- ventral and anterior- posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14. , Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.
Two Tier Hox Collinearity Mediates Vertebrate Axial Patterning. , Durston AJ ., Front Cell Dev Biol. January 1, 2018; 6 102.
A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates. , Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
The RNF146 E3 ubiquitin ligase is required for the control of Wnt signaling and body pattern formation in Xenopus. , Zhu X., Mech Dev. October 1, 2017; 147 28-36.
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.
sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis. , Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.
Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis. , Zhu K ., PLoS One. April 11, 2017; 12 (4): e0175287.
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.
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.
Kdm2a/b Lysine Demethylases Regulate Canonical Wnt Signaling by Modulating the Stability of Nuclear β-Catenin. , Lu L., Dev Cell. June 22, 2015; 33 (6): 660-74.
A time space translation hypothesis for vertebrate axial patterning. , Durston AJ ., Semin Cell Dev Biol. June 1, 2015; 42 86-93.
Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation. , Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
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.
Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein. , Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling. , Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.
Time space translation: a hox mechanism for vertebrate a-p patterning. , Durston A ., Curr Genomics. June 1, 2012; 13 (4): 300-7.
Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning. , Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
The cytoplasmic tyrosine kinase Arg regulates gastrulation via control of actin organization. , Bonacci G., Dev Biol. April 1, 2012; 364 (1): 42-55.
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.
Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus. , Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
Ventx factors function as Nanog-like guardians of developmental potential in Xenopus. , Scerbo P ., PLoS One. January 1, 2012; 7 (5): e36855.
xCITED2 Induces Neural Genes in Animal Cap Explants of Xenopus Embryos. , Yoon J., Exp Neurobiol. September 1, 2011; 20 (3): 123-9.
Hox collinearity - a new perspective. , Durston AJ ., Int J Dev Biol. January 1, 2011; 55 (10-12): 899-908.
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.
BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus. , Wills AE ., Dev Biol. January 15, 2010; 337 (2): 335-50.
PRDC regulates placode neurogenesis in chick by modulating BMP signalling. , Kriebitz NN., Dev Biol. December 15, 2009; 336 (2): 280-92.
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.
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.
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.
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning. , Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus. , Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
Interaction between X- Delta-2 and Hox genes regulates segmentation and patterning of the anteroposterior axis. , Peres JN ., Mech Dev. April 1, 2006; 123 (4): 321-33.
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.
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.
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.
xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development. , Wessely O ., Dev Biol. July 1, 2005; 283 (1): 17-28.
Ethanol exposure affects gene expression in the embryonic organizer and reduces retinoic acid levels. , Yelin R ., Dev Biol. March 1, 2005; 279 (1): 193-204.
Conserved cross-interactions in Drosophila and Xenopus between Ras/ MAPK signaling and the dual-specificity phosphatase MKP3. , Gómez AR., Dev Dyn. March 1, 2005; 232 (3): 695-708.
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.
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.
Timed interactions between the Hox expressing non-organiser mesoderm and the Spemann organiser generate positional information during vertebrate gastrulation. , Wacker SA., Dev Biol. April 1, 2004; 268 (1): 207-19.
PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development. , Yang J ., Development. December 1, 2003; 130 (23): 5569-78.