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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.
Direct nkx2-5 transcriptional repression of isl1 controls cardiomyocyte subtype identity. , Dorn T., Stem Cells. April 1, 2015; 33 (4): 1113-29.
Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo. , Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
Cardiac neural crest is dispensable for outflow tract septation in Xenopus. , Lee YH ., Development. May 1, 2011; 138 (10): 2025-34.
The BMP pathway acts to directly regulate Tbx20 in the developing heart. , Mandel EM ., Development. June 1, 2010; 137 (11): 1919-29.
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.
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 amphibian second heart field: Xenopus islet-1 is required for cardiovascular development. , Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.
SHP-2 is required for the maintenance of cardiac progenitors. , Langdon YG ., Development. November 1, 2007; 134 (22): 4119-30.
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.