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The Journal of Biological Chemistry
|
August 21, 2002
Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy
Paul Robinson, Mahmooda Mirza, Adam Knott, et al.
The Journal of Biological Chemistry
|
June 1, 2005
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype
Mahmooda Mirza, Steven Marston, Ruth Willott, et al.
The Biochemical Journal
|
November 17, 2011
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy
Minttu Marttila, Elina Lemola, William Wallefeld, et al.
Plos One
|
September 26, 2015
OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
Steven Marston, Cecile Montgiraud, Alex B Munster, 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.
Human Molecular Genetics
|
July 27, 2013
Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients
Steven Marston, Massimiliano Memo, Andrew Messer, 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.
Annals of Neurology
|
March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportion
Nigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
April 23, 2013
Mechanical and energetic properties of papillary muscle from ACTC E99K transgenic mouse models of hypertrophic cardiomyopathy
Weihua Song, Petr G Vikhorev, Mavin N Kashyap, et al.
Journal of Molecular and Cellular Cardiology
|
July 6, 2010
Investigation of a transgenic mouse model of familial dilated cardiomyopathy
Weihua Song, Emma Dyer, Daniel Stuckey, et al.
Page
of 4
Search research articles
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Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
The Journal of Biological Chemistry
|
August 21, 2002
Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy
Paul Robinson, Mahmooda Mirza, Adam Knott, et al.
The Journal of Biological Chemistry
|
June 1, 2005
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype
Mahmooda Mirza, Steven Marston, Ruth Willott, et al.
The Biochemical Journal
|
November 17, 2011
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy
Minttu Marttila, Elina Lemola, William Wallefeld, et al.
Plos One
|
September 26, 2015
OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
Steven Marston, Cecile Montgiraud, Alex B Munster, 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.
Human Molecular Genetics
|
July 27, 2013
Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients
Steven Marston, Massimiliano Memo, Andrew Messer, 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.
Annals of Neurology
|
March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportion
Nigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
April 23, 2013
Mechanical and energetic properties of papillary muscle from ACTC E99K transgenic mouse models of hypertrophic cardiomyopathy
Weihua Song, Petr G Vikhorev, Mavin N Kashyap, et al.
Journal of Molecular and Cellular Cardiology
|
July 6, 2010
Investigation of a transgenic mouse model of familial dilated cardiomyopathy
Weihua Song, Emma Dyer, Daniel Stuckey, et al.
Page
of 4