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Elucidating the Role of the VDAC-ANT Complex in Regulating Mitochondrial Energetics in the Heart

Heart, lung & circulation, 2024-08, Vol.33, p.S475-S475

2024

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AlGaN/GaN-based biosensor for label-free detection of biological activity

Sensors and actuators. B, Chemical, 2013-02, Vol.177, p.577-582

2013

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A Novel Therapy to Prevent Cardiac Hypertrophy in a Troponin I Mutant Mouse Model

Heart, lung & circulation, 2016-08, Vol.25, p.S73-S73

2016

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A Single Cysteine in the Cytoplasmic Loop I-II Region on the Human L-type Calcium Channel Protein is Responsible for Increased Function During Oxidative Stress

Heart, lung & circulation, 2016-08, Vol.25, p.S73-S74

2016

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Role of NAD(P)H oxidase in the regulation of cardiac L-type Ca channel function during acute hypoxia

Cardiovascular research, 2005-09, Vol.67 (4), p.624-635

2005

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145 Oxidative Stress Does not Contribute to the Development of Hypertrophic Cardiomyopathy in a Murine Model of the Disease

Heart, lung & circulation, 2020, Vol.29, p.S100-S100

2020

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Treatment of mdx Mice with Morpholino Oligomers Improves Metabolic Function and Contractility

Heart, lung & circulation, 2016-08, Vol.25, p.S83-S84

2016

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CRISPR-like genome editing tool-mediated down regulation of CAMK2D: A potential role for epigenetics intervention in the treatment of cardiac hypertrophy

Heart, lung & circulation, 2015, Vol.24, p.S177-S177

2015

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Atenolol Reduces the Occurrence of Arrhythmias Induced by Isoproterenol in a Model of Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2021, Vol.30, p.S116-S116

2021

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The L-type Ca(2+) channel as a therapeutic target in heart disease

Current medicinal chemistry, 2009, Vol.16 (26), p.3341

2009

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Identification of Proteins that Mediate Functional Communication Between the L-type Calcium Channel and the Mitochondria

Heart, lung & circulation, 2012, Vol.21, p.S60-S60

2012

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Electrophysiological Characterisation of a Cardiac Calcium Channel Mutant Associated With Sudden Cardiac Death, Cav1.2-L1521I

Heart, lung & circulation, 2024-08, Vol.33, p.S260-S260

2024

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Optimising morpholino oligomer therapy in the treatment of mdx cardiomyopathy

Heart, lung & circulation, 2015, Vol.24, p.S181-S181

2015

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(504) - Storing Hearts at Room Temperature Using Gas Persufflation

The Journal of heart and lung transplantation, 2024-04, Vol.43 (4), p.S250-S250

2024

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Validating the Significance of Ser1487 in the Beta-Adrenergic Regulation of the Alpha Subunit of the Cardiac L-Type Calcium Channel Using a CRISPR/Cas9 Mouse Model

Heart, lung & circulation, 2022, Vol.31, p.S317-S317

2022

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Treatment of mdx Mice with Antisense Oligomers to Induce Exon Skipping of Dystrophin Exon 23 Restores Mitochondrial Function in mdx Cardiomyopathy

Heart, lung & circulation, 2013, Vol.22, p.S234-S234

2013

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A Peptide Derived Against the Alpha-Interacting Domain of the L-type Ca2+ Channel Reduces Ischaemia-Reperfusion Injury In Vivo in Rat Heart and Improves Contractility

Heart, lung & circulation, 2013, Vol.22, p.S54-S54

2013

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Identifying the Site/S of Modification on Human L-type Calcium Channel Protein Isoforms During Oxidative Stress

Heart, lung & circulation, 2013, Vol.22, p.S56-S56

2013

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The Role of the Cytoskeleton in Communication between the L-type Calcium Channel and the Mitochondria in Isolated Cardiac Myocytes

Heart, lung & circulation, 2011, Vol.20, p.S51-S51

2011

Volltextzugriff (PDF)

Electrophysiological Characterisation of Calcium Channel Mutant, Cav1.2-R1586Q, Associated With Long QT Syndrome 8

Heart, lung & circulation, 2023-07, Vol.32, p.S153-S154

2023

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An Omics-Based Screening Tool to Determine the Risk of Developing Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2023-07, Vol.32, p.S142

2023

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Altered Calcium Handling and Phosphorylation State are Associated With the Development of Hypertrophic Cardiomyopathy in a Murine Model of the Disease

Heart, lung & circulation, 2021, Vol.30, p.S116-S116

2021

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Evidence for Significance of Serine 1487 in Beta-Adrenergic Regulation of Cav1.2 Subunit Function

Heart, lung & circulation, 2019, Vol.28, p.S170-S170

2019

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Characterising effects of a peptide directed against the L-type Ca2+ channel on mitochondrial function in hypertrophic cardiomyopathy

Heart, lung & circulation, 2015, Vol.24, p.S176-S176

2015

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Characterising L-type Ca2+ Channel Function and Mitochondrial Function in Two Murine Models of Familial Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2013, Vol.22, p.S228-S228

2013

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Elucidating the Role of the VDAC-ANT Complex in Regulating Mitochondrial Energetics in the Heart

AlGaN/GaN-based biosensor for label-free detection of biological activity

A Novel Therapy to Prevent Cardiac Hypertrophy in a Troponin I Mutant Mouse Model

A Single Cysteine in the Cytoplasmic Loop I-II Region on the Human L-type Calcium Channel Protein is Responsible for Increased Function During Oxidative Stress

Role of NAD(P)H oxidase in the regulation of cardiac L-type Ca channel function during acute hypoxia

145 Oxidative Stress Does not Contribute to the Development of Hypertrophic Cardiomyopathy in a Murine Model of the Disease

Treatment of mdx Mice with Morpholino Oligomers Improves Metabolic Function and Contractility

CRISPR-like genome editing tool-mediated down regulation of CAMK2D: A potential role for epigenetics intervention in the treatment of cardiac hypertrophy

Atenolol Reduces the Occurrence of Arrhythmias Induced by Isoproterenol in a Model of Hypertrophic Cardiomyopathy

The L-type Ca(2+) channel as a therapeutic target in heart disease

Identification of Proteins that Mediate Functional Communication Between the L-type Calcium Channel and the Mitochondria

Electrophysiological Characterisation of a Cardiac Calcium Channel Mutant Associated With Sudden Cardiac Death, Cav1.2-L1521I

Optimising morpholino oligomer therapy in the treatment of mdx cardiomyopathy

(504) - Storing Hearts at Room Temperature Using Gas Persufflation

Validating the Significance of Ser1487 in the Beta-Adrenergic Regulation of the Alpha Subunit of the Cardiac L-Type Calcium Channel Using a CRISPR/Cas9 Mouse Model

Treatment of mdx Mice with Antisense Oligomers to Induce Exon Skipping of Dystrophin Exon 23 Restores Mitochondrial Function in mdx Cardiomyopathy

A Peptide Derived Against the Alpha-Interacting Domain of the L-type Ca2+ Channel Reduces Ischaemia-Reperfusion Injury In Vivo in Rat Heart and Improves Contractility

Identifying the Site/S of Modification on Human L-type Calcium Channel Protein Isoforms During Oxidative Stress

The Role of the Cytoskeleton in Communication between the L-type Calcium Channel and the Mitochondria in Isolated Cardiac Myocytes

Electrophysiological Characterisation of Calcium Channel Mutant, Cav1.2-R1586Q, Associated With Long QT Syndrome 8

An Omics-Based Screening Tool to Determine the Risk of Developing Hypertrophic Cardiomyopathy

Altered Calcium Handling and Phosphorylation State are Associated With the Development of Hypertrophic Cardiomyopathy in a Murine Model of the Disease

Evidence for Significance of Serine 1487 in Beta-Adrenergic Regulation of Cav1.2 Subunit Function

Characterising effects of a peptide directed against the L-type Ca2+ channel on mitochondrial function in hypertrophic cardiomyopathy

Characterising L-type Ca2+ Channel Function and Mitochondrial Function in Two Murine Models of Familial Hypertrophic Cardiomyopathy

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