Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Anatomy Item Literature (3430) Expression Attributions Wiki
XB-ANAT-726

Papers associated with sensory system (and sox11)

Limit to papers also referencing gene:
Show all sensory system papers
???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

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.


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.                                    


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


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.                                          


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.                              


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.                  


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.                                                                


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


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


Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome., Hempel A., J Med Genet. March 1, 2016; 53 (3): 152-62.          


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.                    


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.                            


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


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


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):                                               


Comparative gene expression profiling between optic nerve and spinal cord injury in Xenopus laevis reveals a core set of genes inherent in successful regeneration of vertebrate central nervous system axons., Belrose JL., BMC Genomics. August 5, 2020; 21 (1): 540.                  


Developmental and Injury-induced Changes in DNA Methylation in Regenerative versus Non-regenerative Regions of the Vertebrate Central Nervous System., Reverdatto S., BMC Genomics. January 4, 2022; 23 (1): 2.                      


Influence of Sox protein SUMOylation on neural development and regeneration., Chang KC., Neural Regen Res. March 1, 2022; 17 (3): 477-481.      


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

???pagination.result.page??? 1