Papers associated with neural crest (and six1)

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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.
	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.
	Paracrine regulation of neural crest EMT by placodal MMP28., Gouignard N., PLoS Biol. August 1, 2023; 21 (8): e3002261.
	Zmym4 is required for early cranial gene expression and craniofacial cartilage formation., Jourdeuil K., Front Cell Dev Biol. January 1, 2023; 11 1274788.
	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):
	Dynamic expression of MMP28 during cranial morphogenesis., Gouignard N., Philos Trans R Soc Lond B Biol Sci. October 12, 2020; 375 (1809): 20190559.
	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):
	The neural border: Induction, specification and maturation of the territory that generates neural crest cells., Pla P., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.
	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.
	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.
	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.
	Xenopus Nkx6.3 is a neural plate border specifier required for neural crest development., Zhang Z., PLoS One. December 15, 2014; 9 (12): e115165.
	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.
	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; .
	Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates., Yajima H., BMC Biol. May 29, 2014; 12 40.
	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.
	Identification of Pax3 and Zic1 targets in the developing neural crest., Bae CJ., Dev Biol. February 15, 2014; 386 (2): 473-83.
	Early embryonic specification of vertebrate cranial placodes., Schlosser G., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
	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.
	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.
	Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
	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.
	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.
	Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm., Carmona-Fontaine C., Dev Biol. September 15, 2007; 309 (2): 208-21.
	The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.
	XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms., van Grunsven LA., Dev Biol. June 1, 2007; 306 (1): 34-49.
	Neural induction in Xenopus requires inhibition of Wnt-beta-catenin signaling., Heeg-Truesdell E., Dev Biol. October 1, 2006; 298 (1): 71-86.
	Induction and specification of cranial placodes., Schlosser G., Dev Biol. June 15, 2006; 294 (2): 303-51.
	XNF-ATc3 affects neural convergent extension., Borchers A., Development. May 1, 2006; 133 (9): 1745-55.
	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.
	Evolutionary origins of vertebrate placodes: insights from developmental studies and from comparisons with other deuterostomes., Schlosser G., J Exp Zool B Mol Dev Evol. July 15, 2005; 304 (4): 347-99.
	Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor., Brugmann SA., Development. December 1, 2004; 131 (23): 5871-81.
	Role of BMP signaling and the homeoprotein Iroquois in the specification of the cranial placodal field., Glavic A., Dev Biol. August 1, 2004; 272 (1): 89-103.
	Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.

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