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Summary Anatomy Item Literature (763) Expression Attributions Wiki
XB-ANAT-727

Papers associated with vestibuloauditory system (and fn1)

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TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):                                               

Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB., iScience. September 15, 2023; 26 (9): 107665.                          

Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis., Mills A., Front Physiol. January 1, 2019; 10 431.                                          

Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo., Gouignard N., PLoS One. January 18, 2018; 13 (1): e0191751.                                                          

Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              

Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.                                        

In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity., Kuriyama S., J Cell Biol. July 7, 2014; 206 (1): 113-27.                                

PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B., BMC Dev Biol. June 10, 2011; 11 36.                          

Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.            

Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.      

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.                    

Molecular cloning, expression and partial characterization of Xksy, Xenopus member of the Sky family of receptor tyrosine kinases., Kishi YA., Gene. April 17, 2002; 288 (1-2): 29-40.              

Xenopus ADAM 13 is a metalloprotease required for cranial neural crest-cell migration., Alfandari D, Alfandari D., Curr Biol. June 26, 2001; 11 (12): 918-30.            

Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain., Landesman Y., Mech Dev. May 1, 1997; 63 (2): 199-209.            

Integrin alpha 6 expression is required for early nervous system development in Xenopus laevis., Lallier TE., Development. August 1, 1996; 122 (8): 2539-54.                                  

Expression of a homologue of the deleted in colorectal cancer (DCC) gene in the nervous system of developing Xenopus embryos., Pierceall WE., Dev Biol. December 1, 1994; 166 (2): 654-65.              

Regional specificity of glycoconjugates in Xenopus and axolotl embryos., Slack JM., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 137-53.      

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