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Thomas Scheffold

Showing results (31-40 of 41) with videos related to

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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.
BMC Cardiovascular Disorders|March 10, 2011
Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registryThomas Scheffold, Silke Kullmann, Andreas Huge, et al.
Plos One|December 24, 2011
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defectsMaximilian G Posch, Stephan Waldmuller, Melanie Müller, et al.
Plos One|December 27, 2007
Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain geneBirgit S Budde, Priska Binner, Stephan Waldmüller, 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.
Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
International Journal of Cardiology|August 15, 2009
A network against failing hearts--introducing the German "Competence Network Heart Failure"Felix Mehrhof, Markus Löffler, Götz Gelbrich, et al.
European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.
Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
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.
BMC Cardiovascular Disorders|March 10, 2011
Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registryThomas Scheffold, Silke Kullmann, Andreas Huge, et al.
Plos One|December 24, 2011
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defectsMaximilian G Posch, Stephan Waldmuller, Melanie Müller, et al.
Plos One|December 27, 2007
Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain geneBirgit S Budde, Priska Binner, Stephan Waldmüller, 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.
Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
International Journal of Cardiology|August 15, 2009
A network against failing hearts--introducing the German "Competence Network Heart Failure"Felix Mehrhof, Markus Löffler, Götz Gelbrich, et al.
European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.
Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.
Pageof 5