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Summary Anatomy Item Literature (6354) Expression Attributions Wiki
XB-ANAT-254

Papers associated with oocyte (and sox2)

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Wnt-inducible Lrp6-APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway., Colozza G., Sci Rep. December 9, 2020; 10 (1): 21555.            


Long-term association of a transcription factor with its chromatin binding site can stabilize gene expression and cell fate commitment., Gurdon JB., Proc Natl Acad Sci U S A. June 30, 2020; 117 (26): 15075-15084.            


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


Gene Resistance to Transcriptional Reprogramming following Nuclear Transfer Is Directly Mediated by Multiple Chromatin-Repressive Pathways., Jullien J., Mol Cell. March 2, 2017; 65 (5): 873-884.e8.                        


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.                          


A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.                            


Hierarchical molecular events driven by oocyte-specific factors lead to rapid and extensive reprogramming., Jullien J., Mol Cell. August 21, 2014; 55 (4): 524-36.              


Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus., Colozza G., Differentiation. July 1, 2014; 88 (1): 17-26.                    


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.                              


Par6b regulates the dynamics of apicobasal polarity during development of the stratified Xenopus epidermis., Wang S., PLoS One. October 8, 2013; 8 (10): e76854.                      


Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.                    


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.                        


Foxi2 is an animally localized maternal mRNA in Xenopus, and an activator of the zygotic ectoderm activator Foxi1e., Cha SW., PLoS One. January 1, 2012; 7 (7): e41782.            


Histone variant macroH2A confers resistance to nuclear reprogramming., Pasque V., EMBO J. May 6, 2011; 30 (12): 2373-87.                


Mammalian nuclear transplantation to Germinal Vesicle stage Xenopus oocytes - a method for quantitative transcriptional reprogramming., Halley-Stott RP., Methods. May 1, 2010; 51 (1): 56-65.                  


Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis., Morita H., Development. April 1, 2010; 137 (8): 1315-25.                            


Characterization of somatic cell nuclear reprogramming by oocytes in which a linker histone is required for pluripotency gene reactivation., Jullien J., Proc Natl Acad Sci U S A. March 23, 2010; 107 (12): 5483-8.        


Histone H3 lysine 4 methylation is associated with the transcriptional reprogramming efficiency of somatic nuclei by oocytes., Murata K., Epigenetics Chromatin. February 4, 2010; 3 (1): 4.              


FGF-activated calcium channels control neural gene expression in Xenopus., Lee KW., Biochim Biophys Acta. June 1, 2009; 1793 (6): 1033-40.            


Expression cloning of Xenopus zygote arrest 2 (Xzar2) as a novel epidermalization-promoting factor in early embryos of Xenopus laevis., Nakajima Y., Genes Cells. May 1, 2009; 14 (5): 583-95.                    


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.                            


Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning., Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.                            


Cloning and developmental expression of the soxB2 genes, sox14 and sox21, during Xenopus laevis embryogenesis., Cunningham DD., Int J Dev Biol. January 1, 2008; 52 (7): 999-1004.    


Reprogramming events of mammalian somatic cells induced by Xenopus laevis egg extracts., Miyamoto K., Mol Reprod Dev. October 1, 2007; 74 (10): 1268-77.


Xenopus embryos lacking specific isoforms of the corepressor SMRT develop abnormal heads., Malartre M., Dev Biol. April 15, 2006; 292 (2): 333-43.                    


GDF3, a BMP inhibitor, regulates cell fate in stem cells and early embryos., Levine AJ., Development. January 1, 2006; 133 (2): 209-16.            


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.          


foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.            

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