Papers associated with mesoderm (and isl1)

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	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.
	Generation of iPSC-derived limb progenitor-like cells for stimulating phalange regeneration in the adult mouse., Chen Y., Cell Discov. December 19, 2017; 3 17046.
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis., Hempel A., Dev Biol. April 1, 2017; 424 (1): 28-39.
	Dissecting the pre-placodal transcriptome to reveal presumptive direct targets of Six1 and Eya1 in cranial placodes., Riddiford N., Elife. August 31, 2016; 5
	A Retinoic Acid-Hedgehog Cascade Coordinates Mesoderm-Inducing Signals and Endoderm Competence during Lung Specification., Rankin SA, Rankin SA., Cell Rep. June 28, 2016; 16 (1): 66-78.
	Spatial regulation of cell cohesion by Wnt5a during second heart field progenitor deployment., Li D., Dev Biol. April 1, 2016; 412 (1): 18-31.
	The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
	Direct nkx2-5 transcriptional repression of isl1 controls cardiomyocyte subtype identity., Dorn T., Stem Cells. April 1, 2015; 33 (4): 1113-29.
	Temporal and spatial expression analysis of peripheral myelin protein 22 (Pmp22) in developing Xenopus., Tae HJ., Gene Expr Patterns. January 1, 2015; 17 (1): 26-30.
	Sulf1 influences the Shh morphogen gradient during the dorsal ventral patterning of the neural tube in Xenopus tropicalis., Ramsbottom SA., Dev Biol. July 15, 2014; 391 (2): 207-18.
	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.
	Fgfr signaling is required as the early eye field forms to promote later patterning and morphogenesis of the eye., Atkinson-Leadbeater K., Dev Dyn. May 1, 2014; .
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein., Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
	TBX3 Directs Cell-Fate Decision toward Mesendoderm., Weidgang CE., Stem Cell Reports. August 29, 2013; 1 (3): 248-65.
	MRAS GTPase is a novel stemness marker that impacts mouse embryonic stem cell plasticity and Xenopus embryonic cell fate., Mathieu ME., Development. August 1, 2013; 140 (16): 3311-22.
	sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling., Gibb N., Development. April 1, 2013; 140 (7): 1537-49.
	Islet1-expressing cardiac progenitor cells: a comparison across species., Pandur P., Dev Genes Evol. March 1, 2013; 223 (1-2): 117-29.
	Spatial and temporal expressions of prune reveal a role in Müller gliogenesis during Xenopus retinal development., Bilitou A., Gene. November 1, 2012; 509 (1): 93-103.
	New developments in the second heart field., Zaffran S., Differentiation. July 1, 2012; 84 (1): 17-24.
	Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus., Park BY., Dev Biol. February 1, 2012; 362 (1): 65-75.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	Expression analysis of Runx3 and other Runx family members during Xenopus development., Park BY., Gene Expr Patterns. June 1, 2010; 10 (4-5): 159-66.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Islet-1 is required for ventral neuron survival in Xenopus., Shi Y, Shi Y., Biochem Biophys Res Commun. October 23, 2009; 388 (3): 506-10.
	Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Retinal regeneration in the Xenopus laevis tadpole: a new model system., Vergara MN., Mol Vis. May 18, 2009; 15 1000-13.
	Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis., Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.
	Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.
	DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.
	The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development., Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.
	Wnt5 signaling in vertebrate pancreas development., Kim HJ., BMC Biol. October 24, 2005; 3 23.
	Targeted expression of the dominant-negative FGFR4a in the eye using Xrx1A regulatory sequences interferes with normal retinal development., Zhang L., Development. September 1, 2003; 130 (17): 4177-86.
	Development of the pancreas in Xenopus laevis., Kelly OG., Dev Dyn. August 1, 2000; 218 (4): 615-27.
	The control of Xenopus embryonic primary neurogenesis is mediated by retinoid signalling in the neurectoderm., Sharpe C., Mech Dev. March 1, 2000; 91 (1-2): 69-80.

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