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Response by Methawasin and Granzier to Letter Regarding Article, "Phosphodiesterase 9a Inhibition in Mouse Models of Diastolic Dysfunction"

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Klhl41b orchestrates sarcomere assembly and growth to drive skeletal muscle hypertrophy in vivo.

Diastolic contributors in cardiomyocytes of a cardiometabolic HFpEF-like mouse model.

Kbtbd13 knockdown restores muscle function in a clinically relevant mouse model of nemaline myopathy type 6.

RBM20 isoform regulation by independent transcription start sites adapts alternative splicing in development and disease.

Titin's P-zone domains A164-167 are essential for thick filament structural arrangement.

Rbm20 antisense oligonucleotides alleviate diastolic dysfunction in a mouse model of cardiometabolic heart failure (HFpEF).

Diastolic Dysfunction in Congenital Heart Disease: A Pressure-Volume Loop Analysis of Borderline Left Heart.

Genotype, Phenotypic Severity, and Survival in Pediatric Dilated Cardiomyopathy: A Report From the Pediatric Cardiomyopathy Registry.

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Health-Related Quality of Life in Older Patients With Advanced Heart Failure From Before to 2 Years After Heart Transplantation or Long-Term Mechanical Circulatory Support: Findings From the SUSTAIN-IT Study.

Optimizing Screening Intervals for At-Risk Relatives of Dilated Cardiomyopathy Carrying a TTNtv.

A Recovery-Focused Framework for the Management of Cardiogenic Shock.

Quantitative Analysis of Flavonoid Binding to Tyrosinase by Quartz Crystal Microbalance and Molecular Dynamics.

From Conventional to Nano-Enabled Combination Therapies to Address Therapeutic Challenges of Malaria.

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Subjective cognitive symptoms improve following effective migraine treatment: A patient-reported outcome study.

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