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Summary Anatomy Item Literature (5835) Expression Attributions Wiki
XB-ANAT-2

Papers associated with ectoderm∨derBy=4 (and sox11)

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Xenopus Sox11 Partner Proteins and Functional Domains in Neurogenesis., Singleton KS., Genes (Basel). February 15, 2024; 15 (2):         


The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains., Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.                  


Zmym4 is required for early cranial gene expression and craniofacial cartilage formation., Jourdeuil K., Front Cell Dev Biol. January 1, 2023; 11 1274788.          


Quantitative analysis of transcriptome dynamics provides novel insights into developmental state transitions., Johnson K., BMC Genomics. October 23, 2022; 23 (1): 723.                                  


Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates., Bright AR., EMBO J. May 3, 2021; 40 (9): e104913.                        


Mcrs1 interacts with Six1 to influence early craniofacial and otic development., Neilson KM., Dev Biol. November 1, 2020; 467 (1-2): 39-50.                  


Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. March 3, 2020; 13 (3):                                               


miR-199 plays both positive and negative regulatory roles in Xenopus eye development., Ritter RA., Genesis. March 1, 2020; 58 (3-4): e23354.                        


Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.                      


A transition from SoxB1 to SoxE transcription factors is essential for progression from pluripotent blastula cells to neural crest cells., Buitrago-Delgado E., Dev Biol. December 15, 2018; 444 (2): 50-61.                


The neural border: Induction, specification and maturation of the territory that generates neural crest cells., Pla P., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.    


Identification of retinal homeobox (rax) gene-dependent genes by a microarray approach: The DNA endoglycosylase neil3 is a major downstream component of the rax genetic pathway., Pan Y., Dev Dyn. November 1, 2018; 247 (11): 1199-1210.                            


Histone deacetylase activity has an essential role in establishing and maintaining the vertebrate neural crest., Rao A., Development. August 8, 2018; 145 (15):                           


Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates., Marchak A., Dev Biol. September 1, 2017; 429 (1): 213-224.                    


Foxd4 is essential for establishing neural cell fate and for neuronal differentiation., Sherman JH., Genesis. June 1, 2017; 55 (6):   


Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM., Dev Biol. January 15, 2017; 421 (2): 171-182.                    


Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm., Gaur S., Genesis. June 1, 2016; 54 (6): 334-49.                          


Early neural ectodermal genes are activated by Siamois and Twin during blastula stages., Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.          


Evolutionarily conserved role for SoxC genes in neural crest specification and neuronal differentiation., Uy BR., Dev Biol. January 15, 2015; 397 (2): 282-92.                    


Neural transcription factors: from embryos to neural stem cells., Lee HK., Mol Cells. October 31, 2014; 37 (10): 705-12.    


sox4 and sox11 function during Xenopus laevis eye development., Cizelsky W., PLoS One. July 1, 2013; 8 (7): e69372.              


On becoming neural: what the embryo can tell us about differentiating neural stem cells., Moody SA., Am J Stem Cells. June 30, 2013; 2 (2): 74-94.              


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.                                                                


Specific domains of FoxD4/5 activate and repress neural transcription factor genes to control the progression of immature neural ectoderm to differentiating neural plate., Neilson KM., Dev Biol. May 15, 2012; 365 (2): 363-75.                        


Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm., Pieper M., Development. March 1, 2012; 139 (6): 1175-87.                    


Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo., Lim JW., Development. January 1, 2011; 138 (1): 33-44.                    


Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.                  


Mechanisms driving neural crest induction and migration in the zebrafish and Xenopus laevis., Klymkowsky MW., Cell Adh Migr. January 1, 2010; 4 (4): 595-608.  


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.                              


Notch signaling downstream of foxD5 promotes neural ectodermal transcription factors that inhibit neural differentiation., Yan B., Dev Dyn. June 1, 2009; 238 (6): 1358-65.        


foxD5 plays a critical upstream role in regulating neural ectodermal fate and the onset of neural differentiation., Yan B., Dev Biol. May 1, 2009; 329 (1): 80-95.              


Identification of novel transcripts with differential dorso-ventral expression in Xenopus gastrula using serial analysis of gene expression., Faunes F., Genome Biol. February 11, 2009; 10 (2): R15.                    


Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos., Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.                            


Xenopus Sox3 activates sox2 and geminin and indirectly represses Xvent2 expression to induce neural progenitor formation at the expense of non-neural ectodermal derivatives., Rogers CD., Mech Dev. January 1, 2009; 126 (1-2): 42-55.        


Identification of novel ciliogenesis factors using a new in vivo model for mucociliary epithelial development., Hayes JM., Dev Biol. December 1, 2007; 312 (1): 115-30.                                          


Grainyhead-like 3, a transcription factor identified in a microarray screen, promotes the specification of the superficial layer of the embryonic epidermis., Chalmers AD., Mech Dev. September 1, 2006; 123 (9): 702-18.                                                  


Identification of neural genes using Xenopus DNA microarrays., Shin Y., Dev Dyn. February 1, 2005; 232 (2): 432-44.            


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.                                    


Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor., Brugmann SA., Development. December 1, 2004; 131 (23): 5871-81.                    


Involvement of NLK and Sox11 in neural induction in Xenopus development., Hyodo-Miura J., Genes Cells. May 1, 2002; 7 (5): 487-96.                  


Expression of sox11 gene duplicates in zebrafish suggests the reciprocal loss of ancestral gene expression patterns in development., de Martino S., Dev Dyn. March 1, 2000; 217 (3): 279-92.

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