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

Papers associated with vestibuloauditory system (and fgf8)

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


Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans., Lansdon LA., Genetics. January 1, 2018; 208 (1): 283-296.                  


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.                              


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.                    


Distal expression of sprouty (spry) genes during Xenopus laevis limb development and regeneration., Wang YH., Gene Expr Patterns. May 1, 2014; 15 (1): 61-6.                                                  


Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.                                                    


Role of Sp5 as an essential early regulator of neural crest specification in xenopus., Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.                


Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.                  


RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm., Janesick A., Development. March 1, 2012; 139 (6): 1213-24.                        


Regulation of XFGF8 gene expression through SRY (sex-determining region Y)-box 2 in developing Xenopus embryos., Kim YH., Reprod Fertil Dev. January 1, 2012; 24 (6): 769-77.


Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling., Day RC., BMC Dev Biol. January 26, 2011; 11 54.                                                


Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network., Yan B., Dev Dyn. December 1, 2010; 239 (12): 3467-80.                  


Temporal and spatial expression of FGF ligands and receptors during Xenopus development., Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.                                                                                                        


FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.      


Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.              


Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.      


Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus., Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.                  


Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.              


A ubiquitin-conjugating enzyme, ube2d3.2, regulates xMLK2 and pronephros formation in Xenopus., Jean S., Differentiation. April 1, 2008; 76 (4): 431-41.                  


Expression of marker genes during early ear development in medaka., Hochmann S., Gene Expr Patterns. January 1, 2007; 7 (3): 355-62.      


Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.                  


Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination., Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.          


Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles., Beck CW., Mech Dev. September 1, 2006; 123 (9): 674-88.              


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.                    


Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis., Ahrens K., Dev Biol. December 1, 2005; 288 (1): 40-59.            


XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.                  


Expression patterns of Xenopus FGF receptor-like 1/nou-darake in early Xenopus development resemble those of planarian nou-darake and Xenopus FGF8., Hayashi S., Dev Dyn. August 1, 2004; 230 (4): 700-7.        


Isthmin is a novel secreted protein expressed as part of the Fgf-8 synexpression group in the Xenopus midbrain-hindbrain organizer., Pera EM., Mech Dev. August 1, 2002; 116 (1-2): 169-72.      


Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo., Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.          


Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning., Nutt SL., Genes Dev. May 1, 2001; 15 (9): 1152-66.                


FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.        

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