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Jens Mogensen

Showing results (11-20 of 78) with videos related to

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Lancet (London, England)|April 9, 2004
Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathyRoss T Murphy, Jens Mogensen, Anthony Shaw, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Recessive Inheritance of a Rare Variant in the Nuclear Mitochondrial Gene for <i>AARS2</i> in Late-Onset Dilated CardiomyopathySøren K Nielsen, Frederikke Hansen, Henrik Daa Schrøder, et al.
Circulation. Cardiovascular Genetics|December 7, 2011
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T geneFerdinando Pasquale, Petros Syrris, Juan Pablo Kaski, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|April 25, 2024
Frequency of misdiagnosis in hypertrophic cardiomyopathySøren K Nielsen, Torsten B Rasmussen, Thomas M Hey, et al.
Journal of the Neurological Sciences|July 19, 2017
DOK7 congenital myasthenia may be associated with severe mitral valve insufficiencyDavid Gaist, Jens Mogensen, Emil Greve Pedersen, et al.
The Journal of Biological Chemistry|June 1, 2005
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotypeMahmooda Mirza, Steven Marston, Ruth Willott, et al.
The FEBS Journal|April 12, 2005
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formationSøren Vang, Thomas J Corydon, Anders D Børglum, et al.
The Journal of Clinical Investigation|January 18, 2003
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutationsJens Mogensen, Toru Kubo, Mauricio Duque, et al.
Frontiers in Cardiovascular Medicine|March 9, 2026
Sickle cell related cardiomyopathy and cardiovascular autonomic dysfunctionJack Hartnett, Niall Connolly, Sandra Quinn, et al.
Pflugers Archiv : European Journal of Physiology|October 6, 2006
Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibresLaura C Preston, Simon Lipscomb, Paul Robinson, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
Lancet (London, England)|April 9, 2004
Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathyRoss T Murphy, Jens Mogensen, Anthony Shaw, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Recessive Inheritance of a Rare Variant in the Nuclear Mitochondrial Gene for <i>AARS2</i> in Late-Onset Dilated CardiomyopathySøren K Nielsen, Frederikke Hansen, Henrik Daa Schrøder, et al.
Circulation. Cardiovascular Genetics|December 7, 2011
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T geneFerdinando Pasquale, Petros Syrris, Juan Pablo Kaski, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|April 25, 2024
Frequency of misdiagnosis in hypertrophic cardiomyopathySøren K Nielsen, Torsten B Rasmussen, Thomas M Hey, et al.
Journal of the Neurological Sciences|July 19, 2017
DOK7 congenital myasthenia may be associated with severe mitral valve insufficiencyDavid Gaist, Jens Mogensen, Emil Greve Pedersen, et al.
The Journal of Biological Chemistry|June 1, 2005
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotypeMahmooda Mirza, Steven Marston, Ruth Willott, et al.
The FEBS Journal|April 12, 2005
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formationSøren Vang, Thomas J Corydon, Anders D Børglum, et al.
The Journal of Clinical Investigation|January 18, 2003
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutationsJens Mogensen, Toru Kubo, Mauricio Duque, et al.
Frontiers in Cardiovascular Medicine|March 9, 2026
Sickle cell related cardiomyopathy and cardiovascular autonomic dysfunctionJack Hartnett, Niall Connolly, Sandra Quinn, et al.
Pflugers Archiv : European Journal of Physiology|October 6, 2006
Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibresLaura C Preston, Simon Lipscomb, Paul Robinson, et al.
Pageof 8