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Circulation
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October 2, 2002
Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarction
Saïd Ghostine, Claire Carrion, Luiz César Guarita Souza, et al.
Cardiovascular Research
|
July 14, 2004
Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice
Lucie 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 patients
Albert 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 mice
Nicolas 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 cardiomyopathy
Jean 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 cardiomyopathy
Takuro 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 cardiomyopathy
Stephan 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 dysfunction
Philippe 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 cardiomyopathy
Felix 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 laminopathies
Takuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Circulation
|
October 2, 2002
Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarction
Saïd Ghostine, Claire Carrion, Luiz César Guarita Souza, et al.
Cardiovascular Research
|
July 14, 2004
Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice
Lucie 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 patients
Albert 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 mice
Nicolas 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 cardiomyopathy
Jean 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 cardiomyopathy
Takuro 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 cardiomyopathy
Stephan 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 dysfunction
Philippe 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 cardiomyopathy
Felix 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 laminopathies
Takuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.
Page
of 3