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Summary Anatomy Item Literature (3426) Expression Attributions Wiki
XB-ANAT-726

Papers associated with sensory system (and dlx5)

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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.


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


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.                          


Ash2l, an obligatory component of H3K4 methylation complexes, regulates neural crest development., Mohammadparast S., Dev Biol. December 1, 2022; 492 14-24.                                  


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.        


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


Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.          


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):               


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.          


Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing., Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.                    


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.                    


The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.                              


A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements., Square T., Dev Biol. January 15, 2015; 397 (2): 293-304.                                            


Early stages of induction of anterior head ectodermal properties in Xenopus embryos are mediated by transcriptional cofactor ldb1., Plautz CZ., Dev Dyn. December 1, 2014; 243 (12): 1606-18.              


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


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


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


Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis., Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.                                


Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.          


Anuran olfactory bulb organization: embryology, neurochemistry and hodology., Moreno N., Brain Res Bull. March 18, 2008; 75 (2-4): 241-5.


Evidences for tangential migrations in Xenopus telencephalon: developmental patterns and cell tracking experiments., Moreno N., Dev Neurobiol. March 1, 2008; 68 (4): 504-20.                  


An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.                      


The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system., Huang X., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.                        


Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes., von Bubnoff A., Dev Biol. May 15, 2005; 281 (2): 210-26.                                                      


Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus., Chen JA., Mech Dev. March 1, 2005; 122 (3): 307-31.                                                                                                                      


Expression cloning screening of a unique and full-length set of cDNA clones is an efficient method for identifying genes involved in Xenopus neurogenesis., Voigt J., Mech Dev. March 1, 2005; 122 (3): 289-306.                                            


Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.                  


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


Defining pallial and subpallial divisions in the developing Xenopus forebrain., Bachy I., Mech Dev. September 1, 2002; 117 (1-2): 163-72.            


Conserved and divergent patterns of Reelin expression in the zebrafish central nervous system., Costagli A., J Comp Neurol. August 12, 2002; 450 (1): 73-93.    


The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway., Merlo GR., Dev Biol. August 1, 2002; 248 (1): 157-69.


Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation., Hartley KO., Dev Biol. October 1, 2001; 238 (1): 168-84.                


Differential and overlapping expression patterns of X-dll3 and Pax-6 genes suggest distinct roles in olfactory system development of the African clawed frog Xenopus laevis., Franco MD., J Exp Biol. June 1, 2001; 204 (Pt 12): 2049-61.  


Misexpression of Polycomb-group proteins in Xenopus alters anterior neural development and represses neural target genes., Yoshitake Y., Dev Biol. November 15, 1999; 215 (2): 375-87.          


The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals., Pannese M., Mech Dev. April 1, 1998; 73 (1): 73-83.                


Xwnt-8 and lithium can act upon either dorsal mesodermal or neurectodermal cells to cause a loss of forebrain in Xenopus embryos., Fredieu JR., Dev Biol. June 1, 1997; 186 (1): 100-14.                


Cellular and molecular interactions in the development of the Xenopus olfactory system., Reiss JO., Semin Cell Dev Biol. April 1, 1997; 8 (2): 171-9.            


Patterns of distal-less gene expression and inductive interactions in the head of the direct developing frog Eleutherodactylus coqui., Fang H., Dev Biol. October 10, 1996; 179 (1): 160-72.              


Xenopus Distal-less related homeobox genes are expressed in the developing forebrain and are induced by planar signals., Papalopulu N., Development. March 1, 1993; 117 (3): 961-75.          

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