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E Seidman

Showing results (271-280 of 533) with videos related to

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Open Heart|April 29, 2020
Hypertrophic cardiomyopathy in myosin-binding protein C (<i>MYBPC3</i>) Icelandic founder mutation carriersBerglind Adalsteinsdottir, Michael Burke, Barry J Maron, et al.
The Journal of Clinical Investigation|February 6, 2002
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathyMichael Arad, D Woodrow Benson, Antonio R Perez-Atayde, et al.
Circulation|March 26, 2008
Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathyTatiana Tsoutsman, Matthew Kelly, Dominic C H Ng, et al.
Science (New York, N.Y.)|July 4, 1998
Congenital heart disease caused by mutations in the transcription factor NKX2-5J J Schott, D W Benson, C T Basson, et al.
Heart Rhythm|April 29, 2014
Alpha blockade potentiates CPVT therapy in calsequestrin-mutant miceEfrat Kurtzwald-Josefson, Edith Hochhauser, Katia Bogachenko, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Spectrum of somatic mitochondrial mutations in five cancersTatianna C Larman, Steven R DePalma, Angela G Hadjipanayis, et al.
Cell|September 27, 2001
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and diseaseB G Bruneau, G Nemer, J P Schmitt, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 5, 2009
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rodsElena Zvaritch, Natasha Kraeva, Eric Bombardier, et al.
Circulation Research|February 13, 2024
Molecular and Spatial Signatures of Mouse Embryonic Endothelial Cells at Single-Cell ResolutionJian Chen, Xiaoran Zhang, Daniel M DeLaughter, et al.
Circulation|November 28, 2001
Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C geneC I Berul, B K McConnell, H Wakimoto, et al.
Pageof 54

Showing results (271-280 of 533) with videos related to

Sort By:
Pageof 54
Open Heart|April 29, 2020
Hypertrophic cardiomyopathy in myosin-binding protein C (<i>MYBPC3</i>) Icelandic founder mutation carriersBerglind Adalsteinsdottir, Michael Burke, Barry J Maron, et al.
The Journal of Clinical Investigation|February 6, 2002
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathyMichael Arad, D Woodrow Benson, Antonio R Perez-Atayde, et al.
Circulation|March 26, 2008
Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathyTatiana Tsoutsman, Matthew Kelly, Dominic C H Ng, et al.
Science (New York, N.Y.)|July 4, 1998
Congenital heart disease caused by mutations in the transcription factor NKX2-5J J Schott, D W Benson, C T Basson, et al.
Heart Rhythm|April 29, 2014
Alpha blockade potentiates CPVT therapy in calsequestrin-mutant miceEfrat Kurtzwald-Josefson, Edith Hochhauser, Katia Bogachenko, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Spectrum of somatic mitochondrial mutations in five cancersTatianna C Larman, Steven R DePalma, Angela G Hadjipanayis, et al.
Cell|September 27, 2001
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and diseaseB G Bruneau, G Nemer, J P Schmitt, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 5, 2009
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rodsElena Zvaritch, Natasha Kraeva, Eric Bombardier, et al.
Circulation Research|February 13, 2024
Molecular and Spatial Signatures of Mouse Embryonic Endothelial Cells at Single-Cell ResolutionJian Chen, Xiaoran Zhang, Daniel M DeLaughter, et al.
Circulation|November 28, 2001
Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C geneC I Berul, B K McConnell, H Wakimoto, et al.
Pageof 54