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Sakthivel Sadayappan

Showing results (81-90 of 185) with videos related to

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Plos One|November 10, 2017
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosageShiv Kumar Viswanathan, Heather K Sanders, James W McNamara, et al.
Journal of Molecular and Cellular Cardiology|December 3, 2014
Haploinsufficiency of MYBPC3 exacerbates the development of hypertrophic cardiomyopathy in heterozygous miceDavid Barefield, Mohit Kumar, Joshua Gorham, et al.
Journal of Molecular and Cellular Cardiology|December 14, 2016
Cardiac inflammation in genetic dilated cardiomyopathy caused by MYBPC3 mutationThomas L Lynch, Mohamed Ameen Ismahil, Anil G Jegga, et al.
Biorxiv : the Preprint Server for Biology|October 31, 2023
The structural OFF and ON states of myosin can be decoupled from the biochemical super-relaxed and disordered-relaxed statesWeikang Ma, Vivek P Jani, Taejeong Song, et al.
PNAS Nexus|February 8, 2024
The structural OFF and ON states of myosin can be decoupled from the biochemical super- and disordered-relaxed statesVivek P Jani, Taejeong Song, Chengqian Gao, et al.
Journal of Muscle Research and Cell Motility|April 25, 2012
Protein kinase C depresses cardiac myocyte power output and attenuates myofilament responses induced by protein kinase AAaron C Hinken, Laurin M Hanft, Sarah B Scruggs, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 7, 2007
Role of the acidic N' region of cardiac troponin I in regulating myocardial functionSakthivel Sadayappan, Natosha Finley, Jack W Howarth, et al.
Plos One|August 13, 2013
Cardiac myosin binding protein-C plays no regulatory role in skeletal muscle structure and functionBrian Lin, Suresh Govindan, Kyounghwan Lee, et al.
Elife|April 24, 2019
Myonuclear accretion is a determinant of exercise-induced remodeling in skeletal muscleQingnian Goh, Taejeong Song, Michael J Petrany, et al.
International Journal of Cardiology|November 10, 2006
Novel mitochondrial DNA mutations implicated in Noonan syndromePerundurai S Dhandapany, Sakthivel Sadayappan, Ayyasamy Vanniarajan, et al.
Pageof 19

Showing results (81-90 of 185) with videos related to

Sort By:
Pageof 19
Plos One|November 10, 2017
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosageShiv Kumar Viswanathan, Heather K Sanders, James W McNamara, et al.
Journal of Molecular and Cellular Cardiology|December 3, 2014
Haploinsufficiency of MYBPC3 exacerbates the development of hypertrophic cardiomyopathy in heterozygous miceDavid Barefield, Mohit Kumar, Joshua Gorham, et al.
Journal of Molecular and Cellular Cardiology|December 14, 2016
Cardiac inflammation in genetic dilated cardiomyopathy caused by MYBPC3 mutationThomas L Lynch, Mohamed Ameen Ismahil, Anil G Jegga, et al.
Biorxiv : the Preprint Server for Biology|October 31, 2023
The structural OFF and ON states of myosin can be decoupled from the biochemical super-relaxed and disordered-relaxed statesWeikang Ma, Vivek P Jani, Taejeong Song, et al.
PNAS Nexus|February 8, 2024
The structural OFF and ON states of myosin can be decoupled from the biochemical super- and disordered-relaxed statesVivek P Jani, Taejeong Song, Chengqian Gao, et al.
Journal of Muscle Research and Cell Motility|April 25, 2012
Protein kinase C depresses cardiac myocyte power output and attenuates myofilament responses induced by protein kinase AAaron C Hinken, Laurin M Hanft, Sarah B Scruggs, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 7, 2007
Role of the acidic N' region of cardiac troponin I in regulating myocardial functionSakthivel Sadayappan, Natosha Finley, Jack W Howarth, et al.
Plos One|August 13, 2013
Cardiac myosin binding protein-C plays no regulatory role in skeletal muscle structure and functionBrian Lin, Suresh Govindan, Kyounghwan Lee, et al.
Elife|April 24, 2019
Myonuclear accretion is a determinant of exercise-induced remodeling in skeletal muscleQingnian Goh, Taejeong Song, Michael J Petrany, et al.
International Journal of Cardiology|November 10, 2006
Novel mitochondrial DNA mutations implicated in Noonan syndromePerundurai S Dhandapany, Sakthivel Sadayappan, Ayyasamy Vanniarajan, et al.
Pageof 19