Papers associated with embryonic structure (and tnni3)

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	Expression cloning of a human B1 bradykinin receptor., Menke JG., J Biol Chem. August 26, 1994; 269 (34): 21583-6.
	Cardiac troponin I is a heart-specific marker in the Xenopus embryo: expression during abnormal heart morphogenesis., Drysdale TA., Dev Biol. October 1, 1994; 165 (2): 432-41.
	Overexpression of the tinman-related genes XNkx-2.5 and XNkx-2.3 in Xenopus embryos results in myocardial hyperplasia., Cleaver OB., Development. November 1, 1996; 122 (11): 3549-56.
	Retinoic acid can block differentiation of the myocardium after heart specification., Drysdale TA., Dev Biol. August 15, 1997; 188 (2): 205-15.
	Differential expression of nucleoside diphosphate kinases (NDPK/NM23) during Xenopus early development., Ouatas T., Int J Dev Biol. January 1, 1998; 42 (1): 43-52.
	Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant manner., Fu Y., Development. November 1, 1998; 125 (22): 4439-49.
	Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory mutants of the tinman-related genes, XNkx2-3 and XNkx2-5., Grow MW., Dev Biol. December 1, 1998; 204 (1): 187-96.
	The homeobox gene Pitx2: mediator of asymmetric left-right signaling in vertebrate heart and gut looping., Campione M., Development. March 1, 1999; 126 (6): 1225-34.
	The lefty-related factor Xatv acts as a feedback inhibitor of nodal signaling in mesoderm induction and L-R axis development in xenopus., Cheng AM., Development. March 1, 2000; 127 (5): 1049-61.
	BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.
	Serrate and Notch specify cell fates in the heart field by suppressing cardiomyogenesis., Rones MS., Development. September 1, 2000; 127 (17): 3865-76.
	Fox (forkhead) genes are involved in the dorso-ventral patterning of the Xenopus mesoderm., El-Hodiri H., Int J Dev Biol. January 1, 2001; 45 (1): 265-71.
	Wnt antagonism initiates cardiogenesis in Xenopus laevis., Schneider VA., Genes Dev. February 1, 2001; 15 (3): 304-15.
	Cooperative action of Tbx2 and Nkx2.5 inhibits ANF expression in the atrioventricular canal: implications for cardiac chamber formation., Habets PE., Genes Dev. May 15, 2002; 16 (10): 1234-46.
	The slow isoform of Xenopus troponin I is expressed in developing skeletal muscle but not in the heart., Warkman AS., Mech Dev. July 1, 2002; 115 (1-2): 143-6.
	Dishevelled activates Ca2+ flux, PKC, and CamKII in vertebrate embryos., Sheldahl LC., J Cell Biol. May 26, 2003; 161 (4): 769-77.
	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.
	Regulation of heart size in Xenopus laevis., Garriock RJ., Differentiation. October 1, 2003; 71 (8): 506-15.
	Amphibian cardiac troponin I gene's organization, developmental expression, and regulatory properties are different from its mammalian homologue., Warkman AS., Dev Dyn. February 1, 2004; 229 (2): 275-88.
	Heart induction by Wnt antagonists depends on the homeodomain transcription factor Hex., Foley AC., Genes Dev. February 1, 2005; 19 (3): 387-96.
	Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis., Brown DD., Development. February 1, 2005; 132 (3): 553-63.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	Retinoic acid signaling is essential for formation of the heart tube in Xenopus., Collop AH., Dev Biol. March 1, 2006; 291 (1): 96-109.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.
	Characterization of myeloid cells derived from the anterior ventral mesoderm in the Xenopus laevis embryo., Tashiro S., Dev Growth Differ. October 1, 2006; 48 (8): 499-512.
	Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart., Allen BG., Mech Dev. October 1, 2006; 123 (10): 719-29.
	ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.
	Multiple functions of Cerberus cooperate to induce heart downstream of Nodal., Foley AC., Dev Biol. March 1, 2007; 303 (1): 57-65.
	The left-right axis is regulated by the interplay of Coco, Xnr1 and derrière in Xenopus embryos., Vonica A., Dev Biol. March 1, 2007; 303 (1): 281-94.
	The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development., Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.
	GATA4 and GATA5 are essential for heart and liver development in Xenopus embryos., Haworth KE., BMC Dev Biol. July 28, 2008; 8 74.
	Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1., Movassagh M., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
	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.
	GATA transcription factors integrate Wnt signalling during heart development., Afouda BA., Development. October 1, 2008; 135 (19): 3185-90.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	Wnt6 signaling regulates heart muscle development during organogenesis., Lavery DL., Dev Biol. November 15, 2008; 323 (2): 177-88.
	Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5., Espinoza-Lewis RA., Dev Biol. March 15, 2009; 327 (2): 376-85.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	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.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	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.
	Lymph heart musculature is under distinct developmental control from lymphatic endothelium., Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.
	Claudin5 genes encoding tight junction proteins are required for Xenopus heart formation., Yamagishi M., Dev Growth Differ. September 1, 2010; 52 (7): 665-75.
	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.
	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.
	Tbx5 overexpression favors a first heart field lineage in murine embryonic stem cells and in Xenopus laevis embryos., Herrmann F., Dev Dyn. December 1, 2011; 240 (12): 2634-45.

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