Papers associated with primordium (and myh6)

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	A thioredoxin fold protein Sh3bgr regulates Enah and is necessary for proper sarcomere formation., Jang DG., Dev Biol. September 1, 2015; 405 (1): 1-9.
	Direct nkx2-5 transcriptional repression of isl1 controls cardiomyocyte subtype identity., Dorn T., Stem Cells. April 1, 2015; 33 (4): 1113-29.
	Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4., Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.
	Nkx2.5 is involved in myeloid cell differentiation at anterior ventral blood islands in the Xenopus embryo., Sakata H., Dev Growth Differ. October 1, 2014; 56 (8): 544-54.
	Hhex and Cer1 mediate the Sox17 pathway for cardiac mesoderm formation in embryonic stem cells., Liu Y., Stem Cells. June 1, 2014; 32 (6): 1515-26.
	Wiring the retinal circuits activated by light during early development., Bertolesi GE., Neural Dev. February 13, 2014; 9 3.
	Cyclin D2 is a GATA4 cofactor in cardiogenesis., Yamak A., Proc Natl Acad Sci U S A. January 28, 2014; 111 (4): 1415-20.
	Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y., PLoS One. January 17, 2014; 9 (1): e87294.
	Nonclassical MHC class I-dependent invariant T cells are evolutionarily conserved and prominent from early development in amphibians., Edholm ES., Proc Natl Acad Sci U S A. August 27, 2013; 110 (35): 14342-7.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Expression of a cardiac myosin gene in non-heart tissues of developing frogs., Nath K., Dev Genes Evol. May 1, 2013; 223 (3): 189-93.
	Effective RNAi-mediated β2-microglobulin loss of function by transgenesis in Xenopus laevis., Nedelkovska H., Biol Open. March 15, 2013; 2 (3): 335-42.
	Early development of the thymus in Xenopus laevis., Lee YH, Lee YH., Dev Dyn. February 1, 2013; 242 (2): 164-78.
	Early, nonciliary role for microtubule proteins in left-right patterning is conserved across kingdoms., Lobikin M., Proc Natl Acad Sci U S A. July 31, 2012; 109 (31): 12586-91.
	Developmental expression and cardiac transcriptional regulation of Myh7b, a third myosin heavy chain in the vertebrate heart., Warkman AS., Cytoskeleton (Hoboken). May 1, 2012; 69 (5): 324-35.
	SHP-2 acts via ROCK to regulate the cardiac actin cytoskeleton., Langdon Y., Development. March 1, 2012; 139 (5): 948-57.
	Cloning and expression analysis of interferon-γ-inducible-lysosomal thiol reductase gene in South African clawed frog (Xenopus laevis)., Cui XW., Int Immunopharmacol. December 1, 2011; 11 (12): 2091-7.
	Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning., Fakhro KA., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.
	Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.
	Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.
	The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM., Development. June 1, 2010; 137 (11): 1919-29.
	Paralysis and delayed Z-disc formation in the Xenopus tropicalis unc45b mutant dicky ticker., Geach TJ., BMC Dev Biol. January 22, 2010; 10 75.
	FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.
	Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6., Abu-Daya A., Dev Biol. December 1, 2009; 336 (1): 20-9.
	Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/CREB pathway., Keren-Politansky A., Dev Biol. November 15, 2009; 335 (2): 374-84.
	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.
	Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Induction and modulation of smooth muscle differentiation in Xenopus embryonic cells., Barillot W., Dev Dyn. November 1, 2008; 237 (11): 3373-86.
	GATA transcription factors integrate Wnt signalling during heart development., Afouda BA., Development. October 1, 2008; 135 (19): 3185-90.
	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.
	Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1., Movassagh M., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
	IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.
	Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.
	The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.
	SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG., Development. November 1, 2007; 134 (22): 4119-30.
	Multiple functions of Cerberus cooperate to induce heart downstream of Nodal., Foley AC., Dev Biol. March 1, 2007; 303 (1): 57-65.
	Xenopus as a model system for vertebrate heart development., Warkman AS., Semin Cell Dev Biol. February 1, 2007; 18 (1): 46-53.
	Myoskeletin, a factor related to Myocardin, is expressed in somites and required for hypaxial muscle formation in Xenopus., Zhao H., Int J Dev Biol. January 1, 2007; 51 (4): 315-20.
	Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.
	Retinoic acid signaling is essential for formation of the heart tube in Xenopus., Collop AH., Dev Biol. March 1, 2006; 291 (1): 96-109.
	The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis., Huot ME., Mol Biol Cell. September 1, 2005; 16 (9): 4350-61.
	Developmental expression and comparative genomic analysis of Xenopus cardiac myosin heavy chain genes., Garriock RJ., Dev Dyn. August 1, 2005; 233 (4): 1287-93.
	The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart., Smith SJ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.
	Wnt11-R, a protein closely related to mammalian Wnt11, is required for heart morphogenesis in Xenopus., Garriock RJ., Dev Biol. March 1, 2005; 279 (1): 179-92.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.
	Cloning and characterization of Xenopus beta2-microglobulin., Stewart R., Dev Comp Immunol. January 1, 2005; 29 (8): 723-32.
	Phylogenetic conservation of gp96-mediated antigen-specific cellular immunity: new evidence from adoptive cell transfer in xenopus., Maniero GD., Transplantation. November 27, 2004; 78 (10): 1415-21.

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