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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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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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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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A Novel Therapy to Restore Metabolic Activity and Prevent Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2019, Vol.28, p.S156-S156

2019

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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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The Role of Extracellular Matrix Stiffness on Cardiac Metabolic Activity

Heart, lung & circulation, 2019, Vol.28, p.S193-S193

2019

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The Role of Extracellular Matrix Stiffness on Regulation of Cardiac Metabolic Activity: Implications for the Development of Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2018, Vol.27, p.S140-S141

2018

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Identifying the Therapeutic Window for Treatment of Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2017, Vol.26, p.S107-S107

2017

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Testing Efficacy of Branched Dendrimers for the Delivery of a Peptide into Cardiomyocytes

Heart, lung & circulation, 2018, Vol.27, p.S136-S136

2018

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095 Characterising the Phenotypic Switch in a Murine Model of Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2020, Vol.29, p.S79-S80

2020

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Optimal Design of Dendrimer Nanotechnology to Deliver a Peptide as a Therapeutic to the Heart

Heart, lung & circulation, 2019, Vol.28, p.S184-S185

2019

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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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Characterising Mitochondrial Morphology and Signalling in Familial Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2017, Vol.26, p.S104-S104

2017

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Loss of Mitochondrial RNA Binding Protein PTCD1 Leads to Cardiomyopathy

Heart, lung & circulation, 2018, Vol.27, p.S49-S49

2018

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Developing an In Vitro Model of Hypertrophic Cardiomyopathy Using Hydrogel Technology

Heart, lung & circulation, 2018, Vol.27, p.S91-S91

2018

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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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Misregulation of Mitochondrial Protein Synthesis Leads to Cardiomyopathy

Heart, lung & circulation, 2019, Vol.28, p.S147-S147

2019

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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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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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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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Impact of Fluorination on Uptake of Dendrimers by Cardiomyocytes

Heart, lung & circulation, 2017, Vol.26, p.S108-S108

2017

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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

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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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Altered Communication Between the l -Type Ca2+ Channel and VDAC Contributes to Metabolic Inhibition in mdx Cardiomyopathy

Heart, lung & circulation, 2012, Vol.21, p.S54-S54

2012

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

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

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

A Novel Therapy to Restore Metabolic Activity and Prevent Hypertrophic Cardiomyopathy

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

The Role of Extracellular Matrix Stiffness on Cardiac Metabolic Activity

The Role of Extracellular Matrix Stiffness on Regulation of Cardiac Metabolic Activity: Implications for the Development of Hypertrophic Cardiomyopathy

Identifying the Therapeutic Window for Treatment of Hypertrophic Cardiomyopathy

Testing Efficacy of Branched Dendrimers for the Delivery of a Peptide into Cardiomyocytes

095 Characterising the Phenotypic Switch in a Murine Model of Hypertrophic Cardiomyopathy

Optimal Design of Dendrimer Nanotechnology to Deliver a Peptide as a Therapeutic to the Heart

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

Characterising Mitochondrial Morphology and Signalling in Familial Hypertrophic Cardiomyopathy

Loss of Mitochondrial RNA Binding Protein PTCD1 Leads to Cardiomyopathy

Developing an In Vitro Model of Hypertrophic Cardiomyopathy Using Hydrogel Technology

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

Misregulation of Mitochondrial Protein Synthesis Leads to Cardiomyopathy

Optimising morpholino oligomer therapy in the treatment of 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

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

Impact of Fluorination on Uptake of Dendrimers by Cardiomyocytes

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

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

Altered Communication Between the l -Type Ca2+ Channel and VDAC Contributes to Metabolic Inhibition in mdx Cardiomyopathy

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