Papers associated with sensory system (and irx1)

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	The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains., Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
	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;
	Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy., Van de Sompele S., Am J Hum Genet. November 3, 2022; 109 (11): 2029-2048.
	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.
	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.
	Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis., Whitworth GB., Dev Biol. June 15, 2017; 426 (2): 360-373.
	Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.
	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 conserved barH-like homeobox-2 gene barhl2 acts downstream of orthodentricle-2 and together with iroquois-3 in establishment of the caudal forebrain signaling center induced by Sonic Hedgehog., Juraver-Geslin HA., Dev Biol. December 1, 2014; 396 (1): 107-20.
	HNF1B controls proximal-intermediate nephron segment identity in vertebrates by regulating Notch signalling components and Irx1/2., Heliot C., Development. February 1, 2013; 140 (4): 873-85.
	Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
	Over-expression of atf4 in Xenopus embryos interferes with neurogenesis and eye formation., Liu JT., Dongwuxue Yanjiu. October 1, 2011; 32 (5): 485-91.
	A conserved function of the chromatin ATPase Kismet in the regulation of hedgehog expression., Terriente-Félix A., Dev Biol. February 15, 2011; 350 (2): 382-92.
	The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
	The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B., Dev Biol. May 1, 2007; 305 (1): 103-19.
	Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation., Liu H., Gene Expr Patterns. August 1, 2006; 6 (6): 632-6.
	Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.
	Xiro homeoproteins coordinate cell cycle exit and primary neuron formation by upregulating neuronal-fate repressors and downregulating the cell-cycle inhibitor XGadd45-gamma., de la Calle-Mustienes E., Mech Dev. November 1, 2002; 119 (1): 69-80.
	Molecular cloning and characterization of dullard: a novel gene required for neural development., Satow R., Biochem Biophys Res Commun. July 5, 2002; 295 (1): 85-91.
	The Xiro-repressed gene CoREST is expressed in Xenopus neural territories., de la Calle-Mustienes E., Mech Dev. January 1, 2002; 110 (1-2): 209-11.
	The Iroquois family of genes: from body building to neural patterning., Cavodeassi F., Development. August 1, 2001; 128 (15): 2847-55.
	Expression of two novel mouse Iroquois homeobox genes during neurogenesis., Cohen DR., Mech Dev. March 1, 2000; 91 (1-2): 317-21.

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