Papers associated with embryo (and eya1)

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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;
	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.
	Eya1 protein distribution during embryonic development of Xenopus laevis., Almasoudi SH., Gene Expr Patterns. December 1, 2021; 42 119213.
	Collective durotaxis along a self-generated stiffness gradient in vivo., Shellard A., Nature. December 1, 2021; 600 (7890): 690-694.
	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.
	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.
	Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos., Naert T., Sci Rep. September 4, 2020; 10 (1): 14662.
	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):
	Znf703 is a novel RA target in the neural plate border., Janesick A., Sci Rep. June 4, 2019; 9 (1): 8275.
	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.
	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.
	A gene regulatory network underlying the formation of pre-placodal ectoderm in Xenopus laevis., Maharana SK., BMC Biol. July 16, 2018; 16 (1): 79.
	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.
	Identification of novel cis-regulatory elements of Eya1 in Xenopus laevis using BAC recombineering., Maharana SK., Sci Rep. November 3, 2017; 7 (1): 15033.
	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.
	Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
	Dissecting the pre-placodal transcriptome to reveal presumptive direct targets of Six1 and Eya1 in cranial placodes., Riddiford N., Elife. August 31, 2016; 5
	In vivo confinement promotes collective migration of neural crest cells., Szabó A., J Cell Biol. June 6, 2016; 213 (5): 543-55.
	E-cadherin is required for cranial neural crest migration in Xenopus laevis., Huang C., Dev Biol. March 15, 2016; 411 (2): 159-171.
	Using Xenopus to study genetic kidney diseases., Lienkamp SS., Semin Cell Dev Biol. March 1, 2016; 51 117-24.
	Zic1 controls placode progenitor formation non-cell autonomously by regulating retinoic acid production and transport., Jaurena MB., Nat Commun. June 23, 2015; 6 7476.
	The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
	Xenopus Nkx6.3 is a neural plate border specifier required for neural crest development., Zhang Z., PLoS One. December 15, 2014; 9 (12): e115165.
	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--I: cell type evolution., Patthey C., Dev Biol. May 1, 2014; 389 (1): 82-97.
	The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	Setting appropriate boundaries: fate, patterning and competence at the neural plate border., Groves AK., Dev Biol. May 1, 2014; 389 (1): 2-12.
	Early embryonic specification of vertebrate cranial placodes., Schlosser G., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
	New developments in the second heart field., Zaffran S., Differentiation. July 1, 2012; 84 (1): 17-24.
	Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning., Steventon B., Dev Biol. July 1, 2012; 367 (1): 55-65.
	Transcription factors involved in lens development from the preplacodal ectoderm., Ogino H., Dev Biol. March 15, 2012; 363 (2): 333-47.
	Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm., Pieper M., Development. March 1, 2012; 139 (6): 1175-87.
	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.
	Circadian Cycles of Gene Expression in the Coral, Acropora millepora., Brady AK., PLoS One. January 1, 2011; 6 (9): e25072.
	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.
	Making senses development of vertebrate cranial placodes., Schlosser G., Int Rev Cell Mol Biol. January 1, 2010; 283 129-234.
	Cold-inducible RNA binding protein (CIRP), a novel XTcf-3 specific target gene regulates neural development in Xenopus., van Venrooy S., BMC Dev Biol. August 7, 2008; 8 77.
	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.

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