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Molecular Genetics and Metabolism|August 6, 2008
A missense variant in desmoglein-2 predisposes to dilated cardiomyopathyMaximilian G Posch, Matthias J Posch, Christian Geier, et al.Biological Chemistry|May 23, 2007
Expression of the protein phosphatase 1 inhibitor KEPI is downregulated in breast cancer cell lines and tissues and involved in the regulation of the tumor suppressor EGR1 via the MEK-ERK pathwayKatrin Wenzel, Katjana Daskalow, Florian Herse, et al.Plos One|August 27, 2009
Connective tissue growth factor overexpression in cardiomyocytes promotes cardiac hypertrophy and protection against pressure overloadAnna N Panek, Maximilian G Posch, Natalia Alenina, et al.American Journal of Hypertension|January 3, 2007
The G-231A polymorphism in the endothelin-A receptor gene is associated with lower aortic pressure in patients with dilated cardiomyopathyRalph Telgmann, Bassam A Harb, Cemil Ozcelik, et al.International Journal of Cardiology|July 11, 2008
The Biomaterialbank of the German Competence Network of Heart Failure (CNHF) is a valuable resource for biomedical and genetic researchMaximilian G Posch, Götz Gelbrich, Burkert Pieske, et al.Journal of Medical Genetics|January 18, 2011
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practiceSiv Fokstuen, Analia Munoz, Paola Melacini, et al.Basic Research in Cardiology|September 17, 2008
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathyAndreas Perrot, Shwan Hussein, Volker Ruppert, et al.Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.Plos One|June 16, 2011
Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4Mahdi Moradi Marjaneh, Edwin P Kirk, Maximilian G Posch, et al.Journal of Medical Genetics|September 19, 2009
A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defectsMaximilian G Posch, Michael Gramlich, Margaret Sunde, et al.Pageof 4