Publications — Radcliffe Department of Medicine

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Structural and Signaling Proteins in the Z-disk and their Role in Cardiomyopathies

GEHMLICH K. and Noureddine M., (2023), Frontiers in Physiology

Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2.

Broadway-Stringer S. et al, (2023), Cells, 12

Familial atrial fibrillation mutation M1875T-SCN5A increases early sodium current and dampens the effect of flecainide.

O'Reilly M. et al, (2022), Europace

CRUCIAL FUNCTIONS OF ALPHA-ACTININ2 IN THE EMBRYONIC HEART

Gehmlich K. et al, (2022), HEART, 108, A163 - A164

Basic Research Approaches to Evaluate Cardiac Arrhythmia in Heart Failure and Beyond.

Cumberland MJ. et al, (2022), Front Physiol, 13

The Role of Z-disc Proteins in Myopathy and Cardiomyopathy.

Wadmore K. et al, (2021), Int J Mol Sci, 22

Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant.

Jiang H. et al, (2021), Basic Res Cardiol, 116

Complex Relationship Between Cardiac Fibroblasts and Cardiomyocytes in Health and Disease.

Hall C. et al, (2021), J Am Heart Assoc, 10

Nitric Oxide and Mechano-Electrical Transduction in Cardiomyocytes

BOYCOTT HE. et al, (2021), Frontiers in Physiology, 11

Fluorescent PSC-Derived Cardiomyocyte Reporter Lines: Generation Approaches and Their Applications in Cardiovascular Medicine.

Sontayananon N. et al, (2020), Biology (Basel), 9

A year in the life of the EU-CardioRNA COST action: CA17129 catalysing transcriptomics research in cardiovascular disease

Robinson EL. et al, (2020), Non-coding RNA, 6

Nitric Oxide and Mechano-Electrical Transduction in Cardiomyocytes.

Boycott HE. et al, (2020), Front Physiol, 11

The giant titin: how to evaluate its role in cardiomyopathies.

Azad A. et al, (2019), J Muscle Res Cell Motil, 40, 159 - 167

HspB1 phosphorylation regulates its intramolecular dynamics and mechanosensitive molecular chaperone interaction with filamin C.

Collier MP. et al, (2019), Sci Adv, 5

Genetics of and pathogenic mechanisms in arrhythmogenic right ventricular cardiomyopathy.

Vimalanathan AK. et al, (2018), Biophys Rev, 10, 973 - 982

Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion.

Ehsan M. et al, (2018), J Mol Cell Cardiol, 121, 287 - 296

Non-sarcomeric causes of heart failure.

Gehmlich K. and Ehler E., (2018), Biophys Rev, 10, 943 - 947

RNAseq reveals mechanisms of cardiomyopathy in Mlp-C58G knock-in mice

Ehsan M. et al, (2018), JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 120, 53 - 53

Age- and strain-related aberrant Ca2+ release is associated with sudden cardiac death in the ACTC E99K mouse model of hypertrophic cardiomyopathy.

Rowlands CT. et al, (2017), Am J Physiol Heart Circ Physiol, 313, H1213 - H1226

Mammalian γ2 AMPK regulates intrinsic heart rate.

Yavari A. et al, (2017), Nat Commun, 8

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