Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes.
暂无分享,去创建一个
R. Hetzer | W. Haverkamp | M. Gutberlet | R. Dietz | H. Lehmkuhl | A. Perrot | L. Boldt | C. Ozcelik | M. Posch | G. Schmidt | C. Geier
[1] W. Haverkamp,et al. A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy. , 2008, Molecular genetics and metabolism.
[2] I. V. Van Gelder,et al. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. , 2007, American heart journal.
[3] Y. Pinto,et al. Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene. , 2007, Journal of the American College of Cardiology.
[4] R. Hetzer,et al. Corrected body surface potential mapping , 2007, Biomedizinische Technik. Biomedical engineering.
[5] P. Charron,et al. The genetic bases of cardiomyopathies , 2006 .
[6] B. Soliven,et al. Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy. , 2006, Journal of the American College of Cardiology.
[7] G. Dorn,et al. A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[8] R. Felix,et al. Myocardial viability assessment in patients with highly impaired left ventricular function: comparison of delayed enhancement, dobutamine stress MRI, end-diastolic wall thickness, and TI201-SPECT with functional recovery after revascularization , 2005, European Radiology.
[9] Dudley J Pennell,et al. The histologic basis of late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy. , 2004, Journal of the American College of Cardiology.
[10] E. Kranias,et al. Calcium: Phospholamban: a crucial regulator of cardiac contractility , 2003, Nature Reviews Molecular Cell Biology.
[11] G. Dorn,et al. Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human. , 2003, The Journal of clinical investigation.
[12] Ulrike Mende,et al. Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban , 2003, Science.
[13] Andrew N. Carr,et al. Gender influences on sarcoplasmic reticulum Ca2+-handling in failing human myocardium. , 2001, Journal of molecular and cellular cardiology.
[14] J. Seidman,et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. , 1999, The New England journal of medicine.
[15] M. Böhm,et al. Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy , 2008, Basic Research in Cardiology.
[16] O. Simonetti,et al. An improved MR imaging technique for the visualization of myocardial infarction. , 2001, Radiology.
[17] L. Mestroni,et al. Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy. , 1999, European heart journal.
[18] H. Katus,et al. Frequency and phenotypes of familial dilated cardiomyopathy. , 1998, Journal of the American College of Cardiology.