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Ketty Schwartz

Showing results (11-20 of 21) with videos related to

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Circulation|October 2, 2002
Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarctionSaïd Ghostine, Claire Carrion, Luiz César Guarita Souza, et al.
Cardiovascular Research|July 14, 2004
Asymmetric septal hypertrophy in heterozygous cMyBP-C null miceLucie Carrier, Ralph Knöll, Nicolas Vignier, et al.
Circulation|July 6, 2006
Skeletal myoblast transplantation in ischemic heart failure: long-term follow-up of the first phase I cohort of patientsAlbert A Hagège, Jean-Pierre Marolleau, Jean-Thomas Vilquin, et al.
Circulation Research|July 11, 2009
Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic miceNicolas Vignier, Saskia Schlossarek, Bodvael Fraysse, et al.
European Heart Journal|April 30, 2005
Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathyJean F Forissier, Philippe Charron, Sophie Tezenas du Montcel, et al.
Biochemical and Biophysical Research Communications|April 10, 2007
Structural analysis of four and half LIM protein-2 in dilated cardiomyopathyTakuro Arimura, Takeharu Hayashi, Yuji Matsumoto, et al.
Journal of Molecular and Cellular Cardiology|June 6, 2003
Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathyStephan Waldmüller, Sadayappan Sakthivel, Abdul Vahab Saadi, et al.
Journal of the American College of Cardiology|April 8, 2003
Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunctionPhilippe Menasché, Albert A Hagège, Jean-Thomas Vilquin, et al.
European Heart Journal|May 12, 2009
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathyFelix W Friedrich, Pedro Bausero, Yuli Sun, et al.
Human Molecular Genetics|November 19, 2004
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathiesTakuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Circulation|October 2, 2002
Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarctionSaïd Ghostine, Claire Carrion, Luiz César Guarita Souza, et al.
Cardiovascular Research|July 14, 2004
Asymmetric septal hypertrophy in heterozygous cMyBP-C null miceLucie Carrier, Ralph Knöll, Nicolas Vignier, et al.
Circulation|July 6, 2006
Skeletal myoblast transplantation in ischemic heart failure: long-term follow-up of the first phase I cohort of patientsAlbert A Hagège, Jean-Pierre Marolleau, Jean-Thomas Vilquin, et al.
Circulation Research|July 11, 2009
Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic miceNicolas Vignier, Saskia Schlossarek, Bodvael Fraysse, et al.
European Heart Journal|April 30, 2005
Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathyJean F Forissier, Philippe Charron, Sophie Tezenas du Montcel, et al.
Biochemical and Biophysical Research Communications|April 10, 2007
Structural analysis of four and half LIM protein-2 in dilated cardiomyopathyTakuro Arimura, Takeharu Hayashi, Yuji Matsumoto, et al.
Journal of Molecular and Cellular Cardiology|June 6, 2003
Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathyStephan Waldmüller, Sadayappan Sakthivel, Abdul Vahab Saadi, et al.
Journal of the American College of Cardiology|April 8, 2003
Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunctionPhilippe Menasché, Albert A Hagège, Jean-Thomas Vilquin, et al.
European Heart Journal|May 12, 2009
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathyFelix W Friedrich, Pedro Bausero, Yuli Sun, et al.
Human Molecular Genetics|November 19, 2004
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathiesTakuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.
Pageof 3