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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.
CUG-BP, Elav-like family member 1 (CELF1) is required for normal myofibrillogenesis, morphogenesis, and contractile function in the embryonic heart. , Blech-Hermoni Y., Dev Dyn. August 1, 2016; 245 (8): 854-73.
Tcf21 regulates the specification and maturation of proepicardial cells. , Tandon P ., Development. June 1, 2013; 140 (11): 2409-21.
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.
Retinoic acid signaling is essential for formation of the heart tube in Xenopus. , Collop AH., Dev Biol. March 1, 2006; 291 (1): 96-109.
Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart. , Stennard FA ., Dev Biol. October 15, 2003; 262 (2): 206-24.
BMP signaling is required for heart formation in vertebrates. , Shi Y , Shi Y ., Dev Biol. August 15, 2000; 224 (2): 226-37.
Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments. , Raffin M., Dev Biol. February 15, 2000; 218 (2): 326-40.
The morphology of heart development in Xenopus laevis. , Mohun TJ ., Dev Biol. February 1, 2000; 218 (1): 74-88.
Tbx5 is essential for heart development. , Horb ME ., Development. April 1, 1999; 126 (8): 1739-51.
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.
Retinoic acid can block differentiation of the myocardium after heart specification. , Drysdale TA ., Dev Biol. August 15, 1997; 188 (2): 205-15.
Induction of avian cardiac myogenesis by anterior endoderm. , Schultheiss TM., Development. December 1, 1995; 121 (12): 4203-14.