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Complex Relationship Between Cardiac Fibroblasts and Cardiomyocytes in Health and Disease

Journal of the American Heart Association, 2021-03, Vol.10 (5), p.e019338-e019338

2021

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How low can you go – Insight into the level of mutated protein required to cause pathogenic effects in hypertrophic cardiomyopathy

Journal of Molecular and Cellular Cardiology Plus (Online), 2022-09, Vol.1, p.100009, Article 100009

Gehmlich, Katja

2022

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Structural and signaling proteins in the Z-disk and their role in cardiomyopathies

Frontiers in physiology, 2023-03, Vol.14, p.1143858-1143858

2023

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The Role of Z-disc Proteins in Myopathy and Cardiomyopathy

International journal of molecular sciences, 2021-03, Vol.22 (6), p.3058

2021

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Should young athletes be screened for cardiomyopathies to reduce the burden of sudden cardiac death in athletes?

Biophysical reviews, 2023-06, Vol.15 (3), p.321-327

2023

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The Utilisation of Hydrogels for iPSC-Cardiomyocyte Research

International journal of molecular sciences, 2023-06, Vol.24 (12), p.9995

2023

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Genetics of and pathogenic mechanisms in arrhythmogenic right ventricular cardiomyopathy

Biophysical reviews, 2018-08, Vol.10 (4), p.973-982

2018

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Nitric Oxide and Mechano-Electrical Transduction in Cardiomyocytes

Frontiers in physiology, 2020-12, Vol.11, p.606740

2020

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MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy

Nature communications, 2016-06, Vol.7 (1), p.12120-12120, Article 12120

2016

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Generation of a human iPSC-derived cardiomyocyte/fibroblast engineered heart tissue model [version 1; peer review: 1 approved, 2 approved with reservations]

F1000 research, 2023, Vol.12, p.1224

2023

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

Basic research in cardiology, 2021-12, Vol.116 (1), p.14, Article 14

2021

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How do MYBPC3 mutations cause hypertrophic cardiomyopathy?

Journal of muscle research and cell motility, 2012-05, Vol.33 (1), p.75-80

2012

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Chronic activation of human cardiac fibroblasts in vitro attenuates the reversibility of the myofibroblast phenotype

Scientific reports, 2023-07, Vol.13 (1), p.12137-12137, Article 12137

2023

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

Biology (Basel, Switzerland), 2020-11, Vol.9 (11), p.402

2020

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Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion

Journal of molecular and cellular cardiology, 2018-08, Vol.121, p.287-296

2018

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Exploring Syndecan-4 and MLP and Their Interaction in Primary Cardiomyocytes and H9c2 Cells

Cells (Basel, Switzerland), 2024-06, Vol.13 (11), p.947

2024

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

Frontiers in physiology, 2022-02, Vol.13, p.806366-806366

2022

Volltextzugriff (PDF)

Phenoage and longitudinal changes on transthoracic echocardiography in Alström syndrome: a disease of accelerated ageing?

GeroScience, 2024-04, Vol.46 (2), p.1989-1999

2024

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy

Human molecular genetics, 2008-09, Vol.17 (18), p.2753-2765

2008

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Endurance Training Provokes Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Heterozygous Desmoglein-2 Mutants: Alleviation by Preload Reduction

Biomedicines, 2024-05, Vol.12 (5), p.985

2024

Volltextzugriff (PDF)

Generation of a human iPSC-derived cardiomyocyte/fibroblast engineered heart tissue model [version 2; peer review: 2 approved, 1 approved with reservations]

F1000 research, 2023-01, Vol.12, p.1224-1224

2023

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Changes in the cardiac metabolome caused by perhexiline treatment in a mouse model of hypertrophic cardiomyopathy

Molecular bioSystems, 2015-02, Vol.11 (2), p.564-573

2015

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

Cells (Basel, Switzerland), 2023-02, Vol.12 (5), p.721

2023

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A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

Heart rhythm, 2011-05, Vol.8 (5), p.711-718

2011

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How we name academic prizes matters

Nature human behaviour, 2024-02, Vol.8 (2), p.190

2024

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Complex Relationship Between Cardiac Fibroblasts and Cardiomyocytes in Health and Disease

How low can you go – Insight into the level of mutated protein required to cause pathogenic effects in hypertrophic cardiomyopathy

Structural and signaling proteins in the Z-disk and their role in cardiomyopathies

The Role of Z-disc Proteins in Myopathy and Cardiomyopathy

Should young athletes be screened for cardiomyopathies to reduce the burden of sudden cardiac death in athletes?

The Utilisation of Hydrogels for iPSC-Cardiomyocyte Research

Genetics of and pathogenic mechanisms in arrhythmogenic right ventricular cardiomyopathy

Nitric Oxide and Mechano-Electrical Transduction in Cardiomyocytes

MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy

Generation of a human iPSC-derived cardiomyocyte/fibroblast engineered heart tissue model [version 1; peer review: 1 approved, 2 approved with reservations]

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

How do MYBPC3 mutations cause hypertrophic cardiomyopathy?

Chronic activation of human cardiac fibroblasts in vitro attenuates the reversibility of the myofibroblast phenotype

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

Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion

Exploring Syndecan-4 and MLP and Their Interaction in Primary Cardiomyocytes and H9c2 Cells

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

Phenoage and longitudinal changes on transthoracic echocardiography in Alström syndrome: a disease of accelerated ageing?

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy

Endurance Training Provokes Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Heterozygous Desmoglein-2 Mutants: Alleviation by Preload Reduction

Generation of a human iPSC-derived cardiomyocyte/fibroblast engineered heart tissue model [version 2; peer review: 2 approved, 1 approved with reservations]

Changes in the cardiac metabolome caused by perhexiline treatment in a mouse model of hypertrophic cardiomyopathy

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

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

How we name academic prizes matters

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