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Summary Anatomy Item Literature (6691) Expression Attributions Wiki
XB-ANAT-177

Papers associated with eye (and six1)

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In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives., Griffin C., Dev Biol. February 1, 2024; 506 20-30.


Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;             


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


Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.        


Deep learning is widely applicable to phenotyping embryonic development and disease., Naert T., Development. November 1, 2021; 148 (21):                                                                 


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):                                               


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


Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.                      


Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):                                     


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


Ketamine Modulates Zic5 Expression via the Notch Signaling Pathway in Neural Crest Induction., Shi Y, Shi Y., Front Mol Neurosci. February 7, 2018; 11 9.          


De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development., Gordon CT., Nat Genet. February 1, 2017; 49 (2): 249-255.        


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


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


The requirement of histone modification by PRDM12 and Kdm4a for the development of pre-placodal ectoderm and neural crest in Xenopus., Matsukawa S., Dev Biol. March 1, 2015; 399 (1): 164-176.                    


Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development., Yan B., Dev Dyn. February 1, 2015; 244 (2): 181-210.                          


Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling., Watanabe T., Genesis. October 1, 2014; .


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


Early embryonic specification of vertebrate cranial placodes., Schlosser G., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.


Developmental expression of Pitx2c in Xenopus trigeminal and profundal placodes., Jeong YH., Int J Dev Biol. January 1, 2014; 58 (9): 701-4.        


Transcription factors involved in lens development from the preplacodal ectoderm., Ogino H., Dev Biol. March 15, 2012; 363 (2): 333-47.      


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.                        


Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.                        


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.                                                


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.                  


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


Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR., Sato S., Dev Biol. August 1, 2010; 344 (1): 158-71.  


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.                  


The F-box protein Cdc4/Fbxw7 is a novel regulator of neural crest development in Xenopus laevis., Almeida AD., Neural Dev. January 4, 2010; 5 1.                              


Making senses development of vertebrate cranial placodes., Schlosser G., Int Rev Cell Mol Biol. January 1, 2010; 283 129-234.


Xhairy2 functions in Xenopus lens development by regulating p27(xic1) expression., Murato Y., Dev Dyn. September 1, 2009; 238 (9): 2179-92.              


The Wnt antagonists Frzb-1 and Crescent locally regulate basement membrane dissolution in the developing primary mouth., Dickinson AJ., Development. April 1, 2009; 136 (7): 1071-81.                                      


Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus., Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.                        


Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion., Schlosser G., Dev Biol. August 1, 2008; 320 (1): 199-214.                  


Pleiotropic effects in Eya3 knockout mice., Söker T., BMC Dev Biol. June 23, 2008; 8 118.                    


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


XNF-ATc3 affects neural convergent extension., Borchers A., Development. May 1, 2006; 133 (9): 1745-55.          


Evolutionary origins of vertebrate placodes: insights from developmental studies and from comparisons with other deuterostomes., Schlosser G., J Exp Zool B Mol Dev Evol. July 15, 2005; 304 (4): 347-99.


Role of BMP signaling and the homeoprotein Iroquois in the specification of the cranial placodal field., Glavic A., Dev Biol. August 1, 2004; 272 (1): 89-103.


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


Xenopus Eya1 demarcates all neurogenic placodes as well as migrating hypaxial muscle precursors., David R., Mech Dev. May 1, 2001; 103 (1-2): 189-92.      


Molecular cloning and embryonic expression of Xenopus Six homeobox genes., Ghanbari H., Mech Dev. March 1, 2001; 101 (1-2): 271-7.                                                                        


Xenopus Six1 gene is expressed in neurogenic cranial placodes and maintained in the differentiating lateral lines., Pandur PD., Mech Dev. September 1, 2000; 96 (2): 253-7.    


Cell cycle-regulated phosphorylation of the human SIX1 homeodomain protein., Ford HL., J Biol Chem. July 21, 2000; 275 (29): 22245-54.

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