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Journal of Muscle Research and Cell Motility
|
November 8, 2011
How do MYBPC3 mutations cause hypertrophic cardiomyopathy?
Steven Marston, O'Neal Copeland, Katja Gehmlich, et al.
Frontiers in Physiology
|
April 9, 2020
Pressure Overload Is Associated With Low Levels of Troponin I and Myosin Binding Protein C Phosphorylation in the Hearts of Patients With Aortic Stenosis
O'neal Copeland, Andrew Messer, Andrew Jabbour, et al.
Frontiers in Physiology
|
June 24, 2017
Investigations into the Sarcomeric Protein and Ca<sup>2+</sup>-Regulation Abnormalities Underlying Hypertrophic Cardiomyopathy in Cats (<i>Felix catus</i>)
Andrew E Messer, Jasmine Chan, Alex Daley, et al.
Journal of Muscle Research and Cell Motility
|
May 29, 2013
Tropomyosin isoform expression and phosphorylation in the human heart in health and disease
Steven B Marston, O'Neal Copeland, Andrew E Messer, et al.
Biophysical Journal
|
November 25, 2014
The dilated cardiomyopathy-causing mutation ACTC E361G in cardiac muscle myofibrils specifically abolishes modulation of Ca(2+) regulation by phosphorylation of troponin I
Petr G Vikhorev, Weihua Song, Ross Wilkinson, et al.
Journal of Molecular and Cellular Cardiology
|
September 21, 2010
Analysis of cardiac myosin binding protein-C phosphorylation in human heart muscle
O'Neal Copeland, Sakthivel Sadayappan, Andrew E Messer, et al.
Journal of Muscle Research and Cell Motility
|
August 14, 2010
Investigation of changes in skeletal muscle alpha-actin expression in normal and pathological human and mouse hearts
O'Neal Copeland, Kristen J Nowak, Nigel G Laing, et al.
The Journal of Biological Chemistry
|
March 16, 2007
The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments
Mahmooda Mirza, Paul Robinson, Elena Kremneva, et al.
Circulation Research
|
July 4, 2009
Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency
Steven Marston, O'Neal Copeland, Adam Jacques, et al.
Plos One
|
September 26, 2015
OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
Steven Marston, Cecile Montgiraud, Alex B Munster, et al.
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of 2
Search research articles
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Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Journal of Muscle Research and Cell Motility
|
November 8, 2011
How do MYBPC3 mutations cause hypertrophic cardiomyopathy?
Steven Marston, O'Neal Copeland, Katja Gehmlich, et al.
Frontiers in Physiology
|
April 9, 2020
Pressure Overload Is Associated With Low Levels of Troponin I and Myosin Binding Protein C Phosphorylation in the Hearts of Patients With Aortic Stenosis
O'neal Copeland, Andrew Messer, Andrew Jabbour, et al.
Frontiers in Physiology
|
June 24, 2017
Investigations into the Sarcomeric Protein and Ca<sup>2+</sup>-Regulation Abnormalities Underlying Hypertrophic Cardiomyopathy in Cats (<i>Felix catus</i>)
Andrew E Messer, Jasmine Chan, Alex Daley, et al.
Journal of Muscle Research and Cell Motility
|
May 29, 2013
Tropomyosin isoform expression and phosphorylation in the human heart in health and disease
Steven B Marston, O'Neal Copeland, Andrew E Messer, et al.
Biophysical Journal
|
November 25, 2014
The dilated cardiomyopathy-causing mutation ACTC E361G in cardiac muscle myofibrils specifically abolishes modulation of Ca(2+) regulation by phosphorylation of troponin I
Petr G Vikhorev, Weihua Song, Ross Wilkinson, et al.
Journal of Molecular and Cellular Cardiology
|
September 21, 2010
Analysis of cardiac myosin binding protein-C phosphorylation in human heart muscle
O'Neal Copeland, Sakthivel Sadayappan, Andrew E Messer, et al.
Journal of Muscle Research and Cell Motility
|
August 14, 2010
Investigation of changes in skeletal muscle alpha-actin expression in normal and pathological human and mouse hearts
O'Neal Copeland, Kristen J Nowak, Nigel G Laing, et al.
The Journal of Biological Chemistry
|
March 16, 2007
The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments
Mahmooda Mirza, Paul Robinson, Elena Kremneva, et al.
Circulation Research
|
July 4, 2009
Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency
Steven Marston, O'Neal Copeland, Adam Jacques, et al.
Plos One
|
September 26, 2015
OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
Steven Marston, Cecile Montgiraud, Alex B Munster, et al.
Page
of 2