Adam M Jacques

发表

Evidence From Human Myectomy Samples That MYBPC3 Mutations Cause Hypertrophic Cardiomyopathy Through Haploinsufficiency*

H. Watkins, V. Tsang, W. McKenna, 2009, Circulation research.

Ischemic preconditioning-an unfulfilled promise.

Kalpa de Silva, Timothy M. Williams, R. Waksman, 2015, Cardiovascular revascularization medicine : including molecular interventions.

The smoking-dyslipidaemia dyad: A potent synergistic risk for atherosclerotic coronary artery disease

V. Prakash, Pankaj Sharma, Adam M Jacques, 2021, JRSM cardiovascular disease.

The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy

H. Watkins, V. Tsang, S. Harding, 2008, Cardiovascular research.

From genotype to phenotype: a longitudinal study of a patient with hypertrophic cardiomyopathy due to a mutation in the MYBPC3 gene

Steven B Marston, Adam M Jacques, J. Kentish, 2009, Journal of Muscle Research and Cell Motility.

Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T.

D. Ward, C. D. dos Remedios, W. McKenna, 2013, Cardiovascular research.

Functional Analysis of a Unique Troponin C Mutation, GLY159ASP, that Causes Familial Dilated Cardiomyopathy, Studied in Explanted Heart Muscle

D. Ward, J. Kaski, Steven B Marston, 2009, Circulation. Heart failure.

Donor hearts in the Sydney Heart Bank: reliable control but is it ‘normal’ heart?

M. Papadaki, Steven B Marston, Adam M Jacques, 2020, Biophysical Reviews.

Troponin phosphorylation and regulatory function in human heart muscle: dephosphorylation of Ser23/24 on troponin I could account for the contractile defect in end-stage heart failure.

Steven B Marston, Adam M Jacques, A. Messer, 2007, Journal of molecular and cellular cardiology.

Myosin binding protein C phosphorylation in normal, hypertrophic and failing human heart muscle.

V. Tsang, W. McKenna, Steven B Marston, 2008, Journal of molecular and cellular cardiology.

Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy

H. Watkins, V. Tsang, C. D. dos Remedios, 2010, Journal of molecular and cellular cardiology.

Optical coherence tomography in coronary atherosclerosis

Adam M Jacques, M. Mahmoudi, N. Shah, 2015 .

Evidence for haploinsufficiency as the mechanism of action of MyBP-C mutations that cause HCM

H. Watkins, S. Carballo, C. Redwood, 2008 .

Altered function and post-translational modification of contractile proteins in myectomy samples from HOCM patients

V. Tsang, W. McKenna, Adam M Jacques, 2007 .

Evidence for reduced troponin I phosphorylation and altered troponin function in patients with hypertrophic obstructive cardiomyopathy

V. Tsang, W. McKenna, Steven B Marston, 2006 .