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Proceedings of the National Academy of Sciences of the United States of America|June 20, 2002
Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathyCemil Ozcelik, Bettina Erdmann, Bernhard Pilz, et al.
European Journal of Medical Genetics|April 6, 2010
Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillationMaximilian G Posch, Leif-Hendrik Boldt, Michael Polotzki, et al.
European Journal of Human Genetics : EJHG|February 11, 2010
Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathyVolker Ruppert, Thomas Meyer, Clarissa Struwe, et al.
Pediatric Cardiology|October 31, 2006
Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart diseaseCemil Ozcelik, Nana Bit-Avragim, Anna Panek, et al.
International Journal of Cardiology|June 23, 2009
Plasma HER2 levels are not associated with cardiac function or hypertrophy in control subjects and heart failure patientsMaximilian G Posch, Anna Panek, Andrea Kersten, et al.
Heart Rhythm|March 28, 2009
Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudesMaximilian G Posch, Andreas Perrot, Christian Geier, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 2, 2008
Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathyMaximilian G Posch, Laura Thiemann, Pavol Tomasov, et al.
Disease Markers|December 20, 2008
Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophyCristina Alonso-Montes, Mónica G Castro, Julián R Reguero, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 11, 2007
Dysfunction of dysferlin-deficient heartsKatrin Wenzel, Christian Geier, Fatimunnisa Qadri, et al.
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