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Summary Anatomy Item Literature (24) Expression Attributions Wiki
XB-ANAT-3946

Papers associated with cardiac atrium

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Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E., Sci Rep. February 14, 2017; 7 42506.          


The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly., Smith SJ., Dev Biol. August 15, 2016; 416 (2): 373-88.                                                      


Cloning, functional characterization, and remodeling of K2P3.1 (TASK-1) potassium channels in a porcine model of atrial fibrillation and heart failure., Schmidt C., Heart Rhythm. October 1, 2014; 11 (10): 1798-805.


Congenital heart disease protein 5 associates with CASZ1 to maintain myocardial tissue integrity., Sojka S., Development. August 1, 2014; 141 (15): 3040-9.                


Cardiac expression and atrial fibrillation-associated remodeling of K₂p2.1 (TREK-1) K⁺ channels in a porcine model., Schmidt C., Life Sci. March 3, 2014; 97 (2): 107-15.


Identifying the evolutionary building blocks of the cardiac conduction system., Jensen B., PLoS One. January 1, 2012; 7 (9): e44231.                    


Development of the venous pole of the heart in the frog Xenopus laevis: a morphological study with special focus on the development of the venoatrial connections., Jahr M., Dev Dyn. June 1, 2011; 240 (6): 1518-27.


Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart., Puskaric S., Hum Mol Genet. December 1, 2010; 19 (23): 4625-33.            


The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM., Development. June 1, 2010; 137 (11): 1919-29.                  


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.      


Characterization of hERG1a and hERG1b potassium channels-a possible role for hERG1b in the I (Kr) current., Larsen AP., Pflugers Arch. September 1, 2008; 456 (6): 1137-48.


Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination., Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.          


Left-right lineage analysis of the embryonic Xenopus heart reveals a novel framework linking congenital cardiac defects and laterality disease., Ramsdell AF., Development. April 1, 2006; 133 (7): 1399-410.                    


Atria selective prolongation by NIP-142, an antiarrhythmic agent, of refractory period and action potential duration in guinea pig myocardium., Matsuda T., J Pharmacol Sci. May 1, 2005; 98 (1): 33-40.


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.            


Frzb modulates Wnt-9a-mediated beta-catenin signaling during avian atrioventricular cardiac cushion development., Person AD., Dev Biol. February 1, 2005; 278 (1): 35-48.              


Transcriptional regulation of the cardiac-specific MLC2 gene during Xenopus embryonic development., Latinkic BV., Development. February 1, 2004; 131 (3): 669-79.                    


Left and right contributions to the Xenopus heart: implications for asymmetric morphogenesis., Gormley JP., Dev Genes Evol. August 1, 2003; 213 (8): 390-8.


Expression of muscle LIM protein during early development in Xenopus laevis., Duan LJ., Int J Dev Biol. May 1, 2003; 47 (4): 299-302.        


A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2., Svensson EC., Nat Genet. July 1, 2000; 25 (3): 353-6.


The morphology of heart development in Xenopus laevis., Mohun TJ., Dev Biol. February 1, 2000; 218 (1): 74-88.                    


Confocal imaging of early heart development in Xenopus laevis., Kolker SJ., Dev Biol. February 1, 2000; 218 (1): 64-73.              


Response kinetics and pharmacological properties of heteromeric receptors formed by coassembly of GABA rho- and gamma 2-subunits., Qian H., Proc Biol Sci. December 7, 1999; 266 (1436): 2419-25.


Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB., Kosaki R., Am J Med Genet. January 1, 1999; 82 (1): 70-6.

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