Papers associated with ventral (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
	The myeloid lineage is required for the emergence of a regeneration-permissive environment following Xenopus tail amputation., Aztekin C., Development. February 5, 2020; 147 (3):
	Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J., Dev Dyn. June 1, 2019; 248 (6): 465-476.
	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.
	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.
	Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E., Sci Rep. February 14, 2017; 7 42506.
	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.
	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.
	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.
	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.
	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.
	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	Paralysis and delayed Z-disc formation in the Xenopus tropicalis unc45b mutant dicky ticker., Geach TJ., BMC Dev Biol. January 22, 2010; 10 75.
	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.
	Morphogenesis of the primitive gut tube is generated by Rho/ROCK/myosin II-mediated endoderm rearrangements., Reed RA., Dev Dyn. December 1, 2009; 238 (12): 3111-25.
	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.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	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.
	Convergence and extension at gastrulation require a myosin IIB-dependent cortical actin network., Skoglund P., Development. August 1, 2008; 135 (14): 2435-44.
	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.
	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.
	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.
	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.
	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.
	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.
	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.
	The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner., Palmer S., J Cell Biol. May 28, 2001; 153 (5): 985-98.
	Wnt antagonism initiates cardiogenesis in Xenopus laevis., Schneider VA., Genes Dev. February 1, 2001; 15 (3): 304-15.
	Serrate and Notch specify cell fates in the heart field by suppressing cardiomyogenesis., Rones MS., Development. September 1, 2000; 127 (17): 3865-76.
	Disruption of actin-myosin interactions results in the inhibition of focal adhesion assembly in Xenopus XR1 glial cells., Folsom TD., Glia. May 1, 1999; 26 (3): 245-59.
	Expression of myogenic regulatory factors during muscle development of Xenopus: myogenin mRNA accumulation is limited strictly to secondary myogenesis., Nicolas N., Dev Dyn. November 1, 1998; 213 (3): 309-21.

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