Papers associated with right (and six1)

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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.
	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.
	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.
	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):
	Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development., Tavares ALP., Development. September 1, 2021; 148 (17):
	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.
	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):
	Prdm12 Directs Nociceptive Sensory Neuron Development by Regulating the Expression of the NGF Receptor TrkA., Desiderio S., Cell Rep. March 26, 2019; 26 (13): 3522-3536.e5.
	Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
	Xenopus SOX5 enhances myogenic transcription indirectly through transrepression., Della Gaspera B., Dev Biol. October 15, 2018; 442 (2): 262-275.
	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.
	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.
	Neural crest development in Xenopus requires Protocadherin 7 at the lateral neural crest border., Bradley RS., Mech Dev. February 1, 2018; 149 41-52.
	Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling., Vacca B., Sci Rep. January 19, 2018; 8 (1): 1204.
	Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus., Bae CJ., Biochem Biophys Res Commun. January 15, 2018; 495 (3): 2257-2263.
	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.
	Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates., Marchak A., Dev Biol. September 1, 2017; 429 (1): 213-224.
	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.
	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.
	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 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.
	Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
	The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	Identification of Pax3 and Zic1 targets in the developing neural crest., Bae CJ., Dev Biol. February 15, 2014; 386 (2): 473-83.
	Developmental expression of Pitx2c in Xenopus trigeminal and profundal placodes., Jeong YH., Int J Dev Biol. January 1, 2014; 58 (9): 701-4.
	Sim2 prevents entry into the myogenic program by repressing MyoD transcription during limb embryonic myogenesis., Havis E., Development. June 1, 2012; 139 (11): 1910-20.
	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.
	ΔNp63 is regulated by BMP4 signaling and is required for early epidermal development in Xenopus., Tríbulo C., Dev Dyn. February 1, 2012; 241 (2): 257-69.
	The LIM adaptor protein LMO4 is an essential regulator of neural crest development., Ochoa SD., Dev Biol. January 15, 2012; 361 (2): 313-25.
	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.
	The posteriorizing gene Gbx2 is a direct target of Wnt signalling and the earliest factor in neural crest induction., Li B., Development. October 1, 2009; 136 (19): 3267-78.
	Xhairy2 functions in Xenopus lens development by regulating p27(xic1) expression., Murato Y., Dev Dyn. September 1, 2009; 238 (9): 2179-92.
	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.
	Hairy2-Id3 interactions play an essential role in Xenopus neural crest progenitor specification., Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.

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