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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.
Xenopus leads the way: Frogs as a pioneering model to understand the human brain. , Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.
Foxd4l1.1 negatively regulates transcription of neural repressor ventx1.1 during neuroectoderm formation in Xenopus embryos. , Kumar S , Kumar S ., Sci Rep. October 8, 2020; 10 (1): 16780.
Cdc2-like kinase 2 (Clk2) promotes early neural development in Xenopus embryos. , Virgirinia RP., Dev Growth Differ. August 1, 2019; 61 (6): 365-377.
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.
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.
Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration. , Simon E., Biol Open. October 15, 2017; 6 (10): 1528-1540.
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.
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.
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.
Molecular insights into the origin of the Hox-TALE patterning system. , Hudry B., Elife. March 18, 2014; 3 e01939.
Vertical signalling involves transmission of Hox information from gastrula mesoderm to neurectoderm. , Bardine N., PLoS One. January 1, 2014; 9 (12): e115208.
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.
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.
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.
A hindbrain-repressive Wnt3a/ Meis3/ Tsh1 circuit promotes neuronal differentiation and coordinates tissue maturation. , Elkouby YM., Development. April 1, 2012; 139 (8): 1487-97.
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.
A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus. , Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.
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.
Focal adhesion kinase protein regulates Wnt3a gene expression to control cell fate specification in the developing neural plate. , Fonar Y., Mol Biol Cell. July 1, 2011; 22 (13): 2409-21.
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.
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.
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.
Bone morphogenetic protein 15 ( BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis. , Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
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.
Hairy2- Id3 interactions play an essential role in Xenopus neural crest progenitor specification. , Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.
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 opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
Xenopus Teashirt1 regulates posterior identity in brain and cranial neural crest. , Koebernick K., Dev Biol. October 1, 2006; 298 (1): 312-26.
Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning. , Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
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.
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.
Maternal Xenopus Zic2 negatively regulates Nodal-related gene expression during anteroposterior patterning. , Houston DW ., Development. November 1, 2005; 132 (21): 4845-55.
Neural and eye-specific defects associated with loss of the imitation switch ( ISWI) chromatin remodeler in Xenopus laevis. , Dirscherl SS., Mech Dev. November 1, 2005; 122 (11): 1157-70.
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.