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Quaking Inhibits Doxorubicin-Mediated Cardiotoxicity Through Regulation of Cardiac Circular RNA Expression

Circulation research, 2018-01, Vol.122 (2), p.246-254

2018

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Long-term functional and structural preservation of precision-cut human myocardium under continuous electromechanical stimulation in vitro

Nature communications, 2019-01, Vol.10 (1), p.117-117, Article 117

2019

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SARS-CoV-2 infects and induces cytotoxic effects in human cardiomyocytes

Cardiovascular research, 2020-12, Vol.116 (14), p.2207-2215

2020

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Increased susceptibility of human endothelial cells to infections by SARS-CoV-2 variants

Basic research in cardiology, 2021-07, Vol.116 (1), p.42-42, Article 42

2021

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MicroRNA-365 regulates human cardiac action potential duration

Nature communications, 2022-01, Vol.13 (1), p.220-220, Article 220

2022

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Diabetes Mellitus–Induced Microvascular Destabilization in the Myocardium

Journal of the American College of Cardiology, 2017-01, Vol.69 (2), p.131-143

2017

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Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies

International journal of molecular sciences, 2019-09, Vol.20 (18), p.4381

2019

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Cardiac desmosomal adhesion relies on ideal-, slip- and catch bonds

Scientific reports, 2024-01, Vol.14 (1), p.2555-2555, Article 2555

2024

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The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly

Cells (Basel, Switzerland), 2022-12, Vol.11 (23), p.3906

2022

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Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

Circulation (New York, N.Y.), 2018-04, Vol.137 (15), p.1595-1610

2018

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Vitamin D deficiency and driveline infection in patients with a left ventricular assist device implant

International journal of artificial organs, 2023-04, Vol.46 (4), p.235-240

2023

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Detrimental proarrhythmogenic interaction of Ca2+/calmodulin-dependent protein kinase II and NaV1.8 in heart failure

Nature communications, 2021-11, Vol.12 (1), p.1-13, Article 6586

2021

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Targeting myeloid cell coagulation signaling blocks MAP kinase/TGF-β1-driven fibrotic remodeling in ischemic heart failure

The Journal of clinical investigation, 2023-02, Vol.133 (4), p.1-21

2023

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Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20

Human mutation, 2020-11, Vol.41 (11), p.1931-1943

2020

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Neprilysins regulate muscle contraction and heart function via cleavage of SERCA-inhibitory micropeptides

Nature communications, 2022-07, Vol.13 (1), p.4420-4420, Article 4420

2022

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Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene?

Protein & cell, 2019-06, Vol.10 (6), p.393-394

2019

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Special Issue "Cardiovascular Genetics"

Genes, 2021-03, Vol.12 (4), p.479

2021

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The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients

PloS one, 2013-12, Vol.8 (12), p.e83005-e83005

2013

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Publisher Correction: Long-term functional and structural preservation of precision-cut human myocardium under continuous electromechanical stimulation in vitro

Nature communications, 2019-01, Vol.10 (1), p.532-532, Article 532

2019

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Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin ( DES ) Mutation p.Y122H Leading to a Severe Filament Assembly Defect

Genes, 2019-11, Vol.10 (11), p.918

2019

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Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset

International journal of molecular sciences, 2021-04, Vol.22 (7), p.3786

2021

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High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation

PloS one, 2017-12, Vol.12 (12), p.e0189489-e0189489

2017

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Generation of a TMEM43 knockout human induced pluripotent stem cell line (HDZi003-A-1) using CRISPR/Cas9

Stem cell research, 2024-04, Vol.76, p.103354-103354, Article 103354

2024

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Compound Heterozygous FKTN Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern

International journal of molecular sciences, 2022-06, Vol.23 (12), p.6685

2022

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Plasma Biomarkers of Myocardial Fibrosis and Remodeling in Terminal Heart Failure Patients Supported by Mechanical Circulatory Support Devices

The Journal of heart and lung transplantation, 2008-06, Vol.27 (6), p.589-596

2008

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Quaking Inhibits Doxorubicin-Mediated Cardiotoxicity Through Regulation of Cardiac Circular RNA Expression

Long-term functional and structural preservation of precision-cut human myocardium under continuous electromechanical stimulation in vitro

SARS-CoV-2 infects and induces cytotoxic effects in human cardiomyocytes

Increased susceptibility of human endothelial cells to infections by SARS-CoV-2 variants

MicroRNA-365 regulates human cardiac action potential duration

Diabetes Mellitus–Induced Microvascular Destabilization in the Myocardium

Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies

Cardiac desmosomal adhesion relies on ideal-, slip- and catch bonds

The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly

Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

Vitamin D deficiency and driveline infection in patients with a left ventricular assist device implant

Detrimental proarrhythmogenic interaction of Ca2+/calmodulin-dependent protein kinase II and NaV1.8 in heart failure

Targeting myeloid cell coagulation signaling blocks MAP kinase/TGF-β1-driven fibrotic remodeling in ischemic heart failure

Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20

Neprilysins regulate muscle contraction and heart function via cleavage of SERCA-inhibitory micropeptides

Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene?

Special Issue "Cardiovascular Genetics"

The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients

Publisher Correction: Long-term functional and structural preservation of precision-cut human myocardium under continuous electromechanical stimulation in vitro

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin ( DES ) Mutation p.Y122H Leading to a Severe Filament Assembly Defect

Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset

High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation

Generation of a TMEM43 knockout human induced pluripotent stem cell line (HDZi003-A-1) using CRISPR/Cas9

Compound Heterozygous FKTN Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern

Plasma Biomarkers of Myocardial Fibrosis and Remodeling in Terminal Heart Failure Patients Supported by Mechanical Circulatory Support Devices

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