Papers associated with mesoderm (and myh6)

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	Characterization of convergent thickening, a major convergence force producing morphogenic movement in amphibians., Shook DR., Elife. April 11, 2022; 11
	Disabled-2: a positive regulator of the early differentiation of myoblasts., Shang N., Cell Tissue Res. September 1, 2020; 381 (3): 493-508.
	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.
	Liver Specification in the Absence of Cardiac Differentiation Revealed by Differential Sensitivity to Wnt/β Catenin Pathway Activation., Haworth K., Front Physiol. January 1, 2019; 10 155.
	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus., Gentsch GE., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.
	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.
	Molecular model for force production and transmission during vertebrate gastrulation., Pfister K., Development. February 15, 2016; 143 (4): 715-27.
	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.
	Contractile activity is required for Z-disc sarcomere maturation in vivo., Geach TJ., Genesis. May 1, 2015; 53 (5): 299-307.
	Direct nkx2-5 transcriptional repression of isl1 controls cardiomyocyte subtype identity., Dorn T., Stem Cells. April 1, 2015; 33 (4): 1113-29.
	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.
	TBX3 Directs Cell-Fate Decision toward Mesendoderm., Weidgang CE., Stem Cell Reports. August 29, 2013; 1 (3): 248-65.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Early development of the thymus in Xenopus laevis., Lee YH, Lee YH., Dev Dyn. February 1, 2013; 242 (2): 164-78.
	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.
	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.
	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.
	Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.
	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.
	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.
	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.
	A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
	SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG., Development. November 1, 2007; 134 (22): 4119-30.
	The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros., Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.
	Multiple functions of Cerberus cooperate to induce heart downstream of Nodal., Foley AC., Dev Biol. March 1, 2007; 303 (1): 57-65.
	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.
	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.
	Spatio-temporal expression of MRF4 transcripts and protein during Xenopus laevis embryogenesis., Della Gaspera B., Dev Dyn. February 1, 2006; 235 (2): 524-9.
	p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	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.
	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.
	Myogenic regulatory factors: redundant or specific functions? Lessons from Xenopus., Chanoine C., Dev Dyn. December 1, 2004; 231 (4): 662-70.
	Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation., Leise WF., Development. April 1, 2004; 131 (8): 1703-15.
	Fibroblast growth factor receptor-1 is essential for in vitro cardiomyocyte development., Dell'Era P., Circ Res. September 5, 2003; 93 (5): 414-20.
	Amphibian in vitro heart induction: a simple and reliable model for the study of vertebrate cardiac development., Ariizumi T., Int J Dev Biol. September 1, 2003; 47 (6): 405-10.
	A single cdk inhibitor, p27Xic1, functions beyond cell cycle regulation to promote muscle differentiation in Xenopus., Vernon AE., Development. January 1, 2003; 130 (1): 71-83.

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