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OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency

PloS one, 2015-09, Vol.10 (9), p.e0138568-e0138568

2015

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In vivo genome and base editing of a human PCSK9 knock-in hypercholesterolemic mouse model

BMC biology, 2019-01, Vol.17 (1), p.4-4, Article 4

2019

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Frequency-dependent signaling in cardiac myocytes

Frontiers in physiology, 2022-09, Vol.13, p.926422-926422

2022

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The long noncoding RNA TUNAR modulates Wnt signaling and regulates human β-cell proliferation

American journal of physiology: endocrinology and metabolism, 2021-04, Vol.320 (4), p.E846-E857

2021

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Myopalladin promotes muscle growth through modulation of the serum response factor pathway

Journal of cachexia, sarcopenia and muscle, 2020-02, Vol.11 (1), p.169-194

2020

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The Degree of Cardiac Remodelling before Overload Relief Triggers Different Transcriptome and miRome Signatures during Reverse Remodelling (RR)-Molecular Signature Differ with the Extent of RR

International journal of molecular sciences, 2020-12, Vol.21 (24), p.9687

2020

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Antisense Therapy Attenuates Phospholamban p.(Arg14del) Cardiomyopathy in Mice and Reverses Protein Aggregation

International journal of molecular sciences, 2022-02, Vol.23 (5), p.2427

2022

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Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

Journal of the American College of Cardiology, 2004-12, Vol.44 (11), p.2192-2201

2004

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Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes

Scientific reports, 2017-11, Vol.7 (1), p.14829-11, Article 14829

2017

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Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model

Human molecular genetics, 2016-09, Vol.25 (17), p.3676-3688

2016

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Epigenetics and Heart Failure

International journal of molecular sciences, 2020-11, Vol.21 (23), p.9010

2020

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A role for membrane shape and information processing in cardiac physiology

Pflügers Archiv, 2015-01, Vol.467 (1), p.167-173

Knoll, R

2015

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Disease-modifying mutations in familial hypertrophic cardiomyopathy: complexity from simplicity

Circulation (New York, N.Y.), 2008-04, Vol.117 (14), p.1775-1777

2008

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Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy

Nature communications, 2021-08, Vol.12 (1), p.5180-5180, Article 5180

2021

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Reversal of calcium cycling defects in advanced heart failure : Toward molecular therapy

Journal of the American College of Cardiology, 2006-11, Vol.48 (9), p.A15-A23

2006

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Titin kinase ubiquitination aligns autophagy receptors with mechanical signals in the sarcomere

EMBO reports, 2021-10, Vol.22 (10), p.e48018-n/a

2021

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Myosin binding protein-C and hypertrophic cardiomyopathy: role of altered C10 domain

Cardiovascular research, 2019-12, Vol.115 (14), p.1943-1945

2019

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Ventricular Assist Device Implantation Corrects Myocardial Lipotoxicity, Reverses Insulin Resistance, and Normalizes Cardiac Metabolism in Patients With Advanced Heart Failure

Circulation (New York, N.Y.), 2012-06, Vol.125 (23), p.2844-2853

2012

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An Approach to Study Shape-Dependent Transcriptomics at a Single Cell Level

Journal of visualized experiments, 2020-11 (165)

2020

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Inhibiting cardiac myeloperoxidase alleviates the relaxation defect in hypertrophic cardiomyocytes

Cardiovascular research, 2022-01, Vol.118 (2), p.517-530

2022

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Association of intronic DNA methylation and hydroxymethylation alterations in the epigenetic etiology of dilated cardiomyopathy

American journal of physiology. Heart and circulatory physiology, 2019-07, Vol.317 (1), p.H168-H180

2019

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Titin M-line insertion sequence 7 is required for proper cardiac function in mice

Journal of cell science, 2021-09, Vol.134 (18)

2021

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Cell shape determines gene expression: cardiomyocyte morphotypic transcriptomes

Basic research in cardiology, 2019-12, Vol.115 (1), p.7-7, Article 7

2019

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OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency

In vivo genome and base editing of a human PCSK9 knock-in hypercholesterolemic mouse model

Frequency-dependent signaling in cardiac myocytes

Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC)

The long noncoding RNA TUNAR modulates Wnt signaling and regulates human β-cell proliferation

Myopalladin promotes muscle growth through modulation of the serum response factor pathway

The Degree of Cardiac Remodelling before Overload Relief Triggers Different Transcriptome and miRome Signatures during Reverse Remodelling (RR)-Molecular Signature Differ with the Extent of RR

Antisense Therapy Attenuates Phospholamban p.(Arg14del) Cardiomyopathy in Mice and Reverses Protein Aggregation

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes

Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model

Epigenetics and Heart Failure

A role for membrane shape and information processing in cardiac physiology

Laminin-α4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells

Disease-modifying mutations in familial hypertrophic cardiomyopathy: complexity from simplicity

Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy

Reversal of calcium cycling defects in advanced heart failure : Toward molecular therapy

Titin kinase ubiquitination aligns autophagy receptors with mechanical signals in the sarcomere

Myosin binding protein-C and hypertrophic cardiomyopathy: role of altered C10 domain

Ventricular Assist Device Implantation Corrects Myocardial Lipotoxicity, Reverses Insulin Resistance, and Normalizes Cardiac Metabolism in Patients With Advanced Heart Failure

An Approach to Study Shape-Dependent Transcriptomics at a Single Cell Level

Inhibiting cardiac myeloperoxidase alleviates the relaxation defect in hypertrophic cardiomyocytes

Association of intronic DNA methylation and hydroxymethylation alterations in the epigenetic etiology of dilated cardiomyopathy

Titin M-line insertion sequence 7 is required for proper cardiac function in mice

Cell shape determines gene expression: cardiomyocyte morphotypic transcriptomes

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