OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency von Marston, Steven, Montgiraud, Cecile, Munster, Alex B, Copeland, O'Neal, Choi, Onjee, Dos Remedios, Cristobal, Messer, Andrew E, Ehler, Elisabeth, Knöll, Ralph

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A post-MI power struggle: adaptations in cardiac power occur at the sarcomere level alongside MyBP-C and RLC phosphorylation von Toepfer, Christopher N, Sikkel, Markus B, Caorsi, Valentina, Vydyanath, Anupama, Torre, Iratxe, Copeland, O'Neal, Lyon, Alexander R, Marston, Steven B, Luther, Pradeep K, Macleod, Kenneth T, West, Timothy G, Ferenczi, Michael A

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Investigations into the Sarcomeric Protein and Ca2+-Regulation Abnormalities Underlying Hypertrophic Cardiomyopathy in Cats (Felix catus) von Messer, Andrew E., Chan, Jasmine, Daley, Alex, Copeland, O'Neal, Marston, Steven B., Connolly, David J.

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Quantifying the Release of Biomarkers of Myocardial Necrosis from Cardiac Myocytes and Intact Myocardium von Marjot, Jack, Kaier, Thomas E, Martin, Eva D, Reji, Shiney S, Copeland, O'Neal, Iqbal, Mohammed, Goodson, Bob, Hamren, Sarah, Harding, Sian E, Marber, Michael S

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Evidence From Human Myectomy Samples That MYBPC3 Mutations Cause Hypertrophic Cardiomyopathy Through Haploinsufficiency von Marston, Steven, Copeland, O‘Neal, Jacques, Adam, Livesey, Karen, Tsang, Victor, McKenna, William J, Jalilzadeh, Shapour, Carballo, Sebastian, Redwood, Charles, Watkins, Hugh

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How do MYBPC3 mutations cause hypertrophic cardiomyopathy? von Marston, Steven, Copeland, O’Neal, Gehmlich, Katja, Schlossarek, Saskia, Carrrier, Lucie

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Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes von Vikhorev, Petr G., Smoktunowicz, Natalia, Munster, Alex B., Copeland, O’Neal, Kostin, Sawa, Montgiraud, Cecile, Messer, Andrew E., Toliat, Mohammad R., Li, Amy, dos Remedios, Cristobal G., Lal, Sean, Blair, Cheavar A., Campbell, Kenneth S., Guglin, Maya, Richter, Manfred, Knöll, Ralph, Marston, Steven B.

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Pressure Overload Is Associated With Low Levels of Troponin I and Myosin Binding Protein C Phosphorylation in the Hearts of Patients With Aortic Stenosis von Copeland, O'neal, Messer, Andrew, Jabbour, Andrew, Poggesi, Corrado, Prasad, Sanjay, Marston, Steven

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The Dilated Cardiomyopathy-Causing Mutation ACTC E361G in Cardiac Muscle Myofibrils Specifically Abolishes Modulation of Ca2+ Regulation by Phosphorylation of Troponin I von Vikhorev, Petr G., Song, Weihua, Wilkinson, Ross, Copeland, O’Neal, Messer, Andrew E., Ferenczi, Michael A., Marston, Steven B.

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Analysis of cardiac myosin binding protein-C phosphorylation in human heart muscle von Copeland, O'Neal, Sadayappan, Sakthivel, Messer, Andrew E, Steinen, Ger J.M, van der Velden, Jolanda, Marston, Steven B

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Tropomyosin isoform expression and phosphorylation in the human heart in health and disease von Marston, Steven B., Copeland, O’Neal, Messer, Andrew E., MacNamara, Elyshia, Nowak, Kristen, Zampronio, Cleidiane G., Ward, Douglas G.

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The dilated cardiomyopathy-causing mutation ACTC E361G in cardiac muscle myofibrils specifically abolishes modulation of Ca(2+) regulation by phosphorylation of troponin I von Vikhorev, Petr G, Song, Weihua, Wilkinson, Ross, Copeland, O'Neal, Messer, Andrew E, Ferenczi, Michael A, Marston, Steven B

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Erratum to: How do MYBPC3 mutations cause hypertrophic cardiomyopathy? von Marston, Steven, Copeland, O’Neal, Gehmlich, Katja, Schlossarek, Saskia, Carrier, Lucie

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Myofibrillar Ca2+ sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T von Bayliss, Christopher R., Jacques, Adam M., Leung, Man-Ching, Ward, Douglas G., Redwood, Charles S., Gallon, Clare E., Copeland, O'Neal, McKenna, William J., dos Remedios, Cristobal, Marston, Steven B., Messer, Andrew E.

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Myosin binding protein C phosphorylation in normal, hypertrophic and failing human heart muscle von Jacques, Adam M, Copeland, O'Neal, Messer, Andrew E, Gallon, Clare E, King, Katie, McKenna, William J, Tsang, Victor T, Marston, Steven B

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Investigations into the Sarcomeric Protein and Ca 2+ -Regulation Abnormalities Underlying Hypertrophic Cardiomyopathy in Cats ( Felix catus ) von Messer, Andrew E, Chan, Jasmine, Daley, Alex, Copeland, O'Neal, Marston, Steven B, Connolly, David J

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Dcm-Causing Mutation E361G in Actin Uncouples Myofibril Ca2+ Sensitivity from Protein Phosphorylation von Vikhorev, Petr G., Wilkinson, Ross, Song, Weihua, Copeland, O'Neal, Ferenczi, Michael A., Marston, Steven B.

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Molecular Mechanism of the E99K Mutation in Cardiac Actin (ACTC Gene) That Causes Apical Hypertrophy in Man and Mouse von Song, Weihua, Dyer, Emma, Stuckey, Daniel J., Copeland, O'Neal, Leung, Man-Ching, Bayliss, Christopher, Messer, Andrew, Wilkinson, Ross, Tremoleda, Jordi Lopez, Schneider, Michael D., Harding, Sian E., Redwood, Charles S., Clarke, Kieran, Nowak, Kristen, Monserrat, Lorenzo, Wells, Dominic, Marston, Steven B.

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The Dilated Cardiomyopathy-Causing Mutation ACTC E361G in Cardiac Muscle Myofibrils Specifically Abolishes Modulation of Ca^sup 2+^ Regulation by Phosphorylation of Troponin I von Vikhorev, Petr G, Song, Weihua, Wilkinson, Ross, Copeland, O'Neal, Messer, Andrew E, Ferenczi, Michael A, Marston, Steven B

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Quantitative Analysis of MyBP-C Phosphorylation in Human Heart using Phosphate Affinity SDS-Page von Marston, Steven, Sadayappan, Sakthivel, Copeland, O'neal

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