Papers associated with mesoderm (and six1)

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	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):
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	Xenopus SOX5 enhances myogenic transcription indirectly through transrepression., Della Gaspera B., Dev Biol. October 15, 2018; 442 (2): 262-275.
	Histone deacetylase activity has an essential role in establishing and maintaining the vertebrate neural crest., Rao A., Development. August 8, 2018; 145 (15):
	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.
	Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates., Marchak A., Dev Biol. September 1, 2017; 429 (1): 213-224.
	Pax2/Pax8-defined subdomains and the occurrence of apoptosis in the posterior placodal area of mice., Washausen S., Brain Struct Funct. August 1, 2017; 222 (6): 2671-2695.
	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 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.
	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.
	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 II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	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.
	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.
	Transcription factors involved in lens development from the preplacodal ectoderm., Ogino H., Dev Biol. March 15, 2012; 363 (2): 333-47.
	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.
	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 Wnt antagonists Frzb-1 and Crescent locally regulate basement membrane dissolution in the developing primary mouth., Dickinson AJ., Development. April 1, 2009; 136 (7): 1071-81.
	Pleiotropic effects in Eya3 knockout mice., Söker T., BMC Dev Biol. June 23, 2008; 8 118.
	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.
	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.
	Dlx proteins position the neural plate border and determine adjacent cell fates., Woda JM., Development. January 1, 2003; 130 (2): 331-42.
	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.

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