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Summary Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-3714

Papers associated with right (and eya1)

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Paracrine regulation of neural crest EMT by placodal MMP28., Gouignard N., PLoS Biol. August 1, 2023; 21 (8): e3002261.                                      


Npr3 regulates neural crest and cranial placode progenitors formation through its dual function as clearance and signaling receptor., Devotta A., Elife. May 10, 2023; 12                                                       


Production and characterization of monoclonal antibodies to Xenopus proteins., Horr B., Development. February 15, 2023; 150 (4):               


Production and characterization of monoclonal antibodies to xenopus proteins., Horr B., Development. February 14, 2023;                 


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


Xenopus Dusp6 modulates FGF signaling to precisely pattern pre-placodal ectoderm., Tsukano K., Dev Biol. August 1, 2022; 488 81-90.                          


Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development., Tavares ALP., Development. September 1, 2021; 148 (17):                       


Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.                                                    


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):                                               


A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):               


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


Shared evolutionary origin of vertebrate neural crest and cranial placodes., Horie R., Nature. August 1, 2018; 560 (7717): 228-232.      


A gene regulatory network underlying the formation of pre-placodal ectoderm in Xenopus laevis., Maharana SK., BMC Biol. July 16, 2018; 16 (1): 79.                            


Six1 and Eya1 both promote and arrest neuronal differentiation by activating multiple Notch pathway genes., Riddiford N., Dev Biol. November 15, 2017; 431 (2): 152-167.                            


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.                    


Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.                  


Dissecting the pre-placodal transcriptome to reveal presumptive direct targets of Six1 and Eya1 in cranial placodes., Riddiford N., Elife. August 31, 2016; 5                                                                         


Using Xenopus to discover new genes involved in branchiootorenal spectrum disorders., Moody SA., Comp Biochem Physiol C Toxicol Pharmacol. December 1, 2015; 178 16-24.


The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.                                            


The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.            


Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning., Steventon B., Dev Biol. July 1, 2012; 367 (1): 55-65.                


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.                        


Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors., Neilson KM., Dev Dyn. December 1, 2010; 239 (12): 3446-66.                                                                          


EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis., Li Y., Biol Cell. February 17, 2010; 102 (5): 277-92.                  


Regulation of otic vesicle and hair cell stereocilia morphogenesis by Ena/VASP-like (Evl) in Xenopus., Wanner SJ., J Cell Sci. August 1, 2007; 120 (Pt 15): 2641-51.          


The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.                


Induction and specification of cranial placodes., Schlosser G., Dev Biol. June 15, 2006; 294 (2): 303-51.                


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.                    


Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.                          


A restrictive role for Hedgehog signalling during otic specification in Xenopus., Koebernick K., Dev Biol. August 15, 2003; 260 (2): 325-38.              

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