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Summary Anatomy Item Literature (21) Expression Attributions Wiki
XB-ANAT-1680

Papers associated with secondary heart field

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Expression of the adhesion G protein-coupled receptor A2 (adgra2) during Xenopus laevis development., Seigfried FA., Gene Expr Patterns. January 1, 2018; 28 54-61.                                      


Frizzled-7 is required for Xenopus heart development., Abu-Elmagd M., Biol Open. December 15, 2017; 6 (12): 1861-1868.            


Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E., Sci Rep. January 1, 2017; 7 42506.          


Spatial regulation of cell cohesion by Wnt5a during second heart field progenitor deployment., Li D., Dev Biol. April 1, 2016; 412 (1): 18-31.  


Mapping the dynamic expression of Wnt11 and the lineage contribution of Wnt11-expressing cells during early mouse development., Sinha T., Dev Biol. February 15, 2015; 398 (2): 177-92.


Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.                                              


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.          


New developments in the second heart field., Zaffran S., Differentiation. July 1, 2012; 84 (1): 17-24.


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.  


Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.                  


Early chordate origins of the vertebrate second heart field., Stolfi A., Science. July 30, 2010; 329 (5991): 565-8.


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.            


XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage., Ito Y., Dev Biol. July 1, 2008; 319 (1): 34-45.                          


The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development., Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.          


Distinct effectors of platelet-derived growth factor receptor-alpha signaling are required for cell survival during embryogenesis., Van Stry M., Proc Natl Acad Sci U S A. June 7, 2005; 102 (23): 8233-8.          


Cardiac neural crest ablation alters Id2 gene expression in the developing heart., Martinsen BJ., Dev Biol. August 1, 2004; 272 (1): 176-90.          


Pitx2c patterns anterior myocardium and aortic arch vessels and is required for local cell movement into atrioventricular cushions., Liu C., Development. November 1, 2002; 129 (21): 5081-91.


Efficient Cre-mediated deletion in cardiac progenitor cells conferred by a 3''UTR-ires-Cre allele of the homeobox gene Nkx2-5., Stanley EG., Int J Dev Biol. January 1, 2002; 46 (4): 431-9.


Conotruncal myocardium arises from a secondary heart field., Waldo KL., Development. August 1, 2001; 128 (16): 3179-88.


Regulation of the tinman homologues in Xenopus embryos., Sparrow DB., Dev Biol. November 1, 2000; 227 (1): 65-79.      

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