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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;
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.
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP., Development. September 1, 2021; 148 (17):
Molecular mechanisms of hearing loss in Nager syndrome. , Maharana SK ., Dev Biol. August 1, 2021; 476 200-208.
Mutations in SIX1 Associated with Branchio-oto-Renal Syndrome (BOR) Differentially Affect Otic Expression of Putative Target Genes. , Mehdizadeh T., J Dev Biol. June 30, 2021; 9 (3):
Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1. , Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
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.
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.
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.
Opportunities and limits of the one gene approach: the ability of Atoh1 to differentiate and maintain hair cells depends on the molecular context. , Jahan I., Front Cell Neurosci. February 5, 2015; 9 26.
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.
Sp8 regulates inner ear development. , Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
Early embryonic specification of vertebrate cranial placodes. , Schlosser G ., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
Probing the Xenopus laevis inner ear transcriptome for biological function. , Powers TR ., BMC Genomics. June 8, 2012; 13 225.
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.
The LIM adaptor protein LMO4 is an essential regulator of neural crest development. , Ochoa SD., Dev Biol. January 15, 2012; 361 (2): 313-25.
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.
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.
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.
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.
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.