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Summary Anatomy Item Literature (5836) Expression Attributions Wiki
XB-ANAT-2

Papers associated with ectoderm (and myf5)

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Mechanical Tensions Regulate Gene Expression in the Xenopus laevis Axial Tissues., Eroshkin FM., Int J Mol Sci. January 10, 2024; 25 (2):         


Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.                                            


Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):                                           


Temporal transcriptomic profiling reveals dynamic changes in gene expression of Xenopus animal cap upon activin treatment., Satou-Kobayashi Y., Sci Rep. July 15, 2021; 11 (1): 14537.          


BMP signaling is enhanced intracellularly by FHL3 controlling WNT-dependent spatiotemporal emergence of the neural crest., Alkobtawi M., Cell Rep. June 22, 2021; 35 (12): 109289.                        


Evolution of Somite Compartmentalization: A View From Xenopus., Della Gaspera B., Front Cell Dev Biol. January 1, 2021; 9 790847.                  


A dual function of FGF signaling in Xenopus left-right axis formation., Schneider I., Development. May 10, 2019; 146 (9):                               


Candidate Heterotaxy Gene FGFR4 Is Essential for Patterning of the Left-Right Organizer in Xenopus., Sempou E., Front Physiol. January 1, 2018; 9 1705.              


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.                                              


Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.                                


ZC4H2 stabilizes Smads to enhance BMP signalling, which is involved in neural development in Xenopus., Ma P., Open Biol. August 1, 2017; 7 (8):                           


Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.                                    


The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.                                            


E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.                  


Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.                            


The RNA-binding protein Rbm24 is transiently expressed in myoblasts and is required for myogenic differentiation during vertebrate development., Grifone R., Mech Dev. November 1, 2014; 134 1-15.  


Inference of the Xenopus tropicalis embryonic regulatory network and spatial gene expression patterns., Zheng Z., BMC Syst Biol. January 8, 2014; 8 3.                  


FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.                              


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus., Lim CY., Development. February 1, 2013; 140 (4): 853-60.                                              


Early transcriptional targets of MyoD link myogenesis and somitogenesis., Maguire RJ., Dev Biol. November 15, 2012; 371 (2): 256-68.                                                    


Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.                                    


Ventx factors function as Nanog-like guardians of developmental potential in Xenopus., Scerbo P., PLoS One. January 1, 2012; 7 (5): e36855.              


Snail2 controls mesodermal BMP/Wnt induction of neural crest., Shi J., Development. August 1, 2011; 138 (15): 3135-45.                  


Origin of muscle satellite cells in the Xenopus embryo., Daughters RS., Development. March 1, 2011; 138 (5): 821-30.                          


Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.                      


Identification and characterization of alternative promoters of zebrafish Rtn-4/Nogo genes in cultured cells and zebrafish embryos., Chen YC., Nucleic Acids Res. August 1, 2010; 38 (14): 4635-50.              


Delta-Notch signaling is involved in the segregation of the three germ layers in Xenopus laevis., Revinski DR., Dev Biol. March 15, 2010; 339 (2): 477-92.            


A conserved MRF4 promoter drives transgenic expression in Xenopus embryonic somites and adult muscle., Hinterberger TJ., Int J Dev Biol. January 1, 2010; 54 (4): 617-25.              


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.                            


Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.                


Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats., Bosnakovski D., PLoS One. September 16, 2009; 4 (9): e7003.          


Diversification of the expression patterns and developmental functions of the dishevelled gene family during chordate evolution., Gray RS., Dev Dyn. August 1, 2009; 238 (8): 2044-57.            


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.                    


Muscular dystrophy candidate gene FRG1 is critical for muscle development., Hanel ML., Dev Dyn. June 1, 2009; 238 (6): 1502-12.        


Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.              


Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          


Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.          


A p38 MAPK-CREB pathway functions to pattern mesoderm in Xenopus., Keren A., Dev Biol. October 1, 2008; 322 (1): 86-94.        


Bmp signaling is necessary and sufficient for ventrolateral endoderm specification in Xenopus., Wills A., Dev Dyn. August 1, 2008; 237 (8): 2177-86.      


The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.        


ANR5, an FGF target gene product, regulates gastrulation in Xenopus., Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.                  


Chordin affects pronephros development in Xenopus embryos by anteriorizing presomitic mesoderm., Mitchell T., Dev Dyn. January 1, 2007; 236 (1): 251-61.          


Myoskeletin, a factor related to Myocardin, is expressed in somites and required for hypaxial muscle formation in Xenopus., Zhao H., Int J Dev Biol. January 1, 2007; 51 (4): 315-20.              


FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    


XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation., Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.                                


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.                    


Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity., Yabe S., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.                        


Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK., Dev Cell. March 1, 2005; 8 (3): 401-11.                          


Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.            

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