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Deficit in PINK1/PARKIN-mediated mitochondrial autophagy at late stages of dystrophic cardiomyopathy

Cardiovascular research, 2018-01, Vol.114 (1), p.90-102

2018

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Transfer and Tunneling of Ca2+ from Sarcoplasmic Reticulum to Mitochondria in Skeletal Muscle

The Journal of biological chemistry, 2006-01, Vol.281 (3), p.1547-1554

2006

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Cardiac phenotype of Duchenne Muscular Dystrophy: Insights from cellular studies

Journal of molecular and cellular cardiology, 2013-05, Vol.58, p.217-224

2013

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Hypersensitivity of excitation-contraction coupling in dystrophic cardiomyocytes

American journal of physiology. Heart and circulatory physiology, 2009-12, Vol.297 (6), p.H1992-H2003

2009

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Reciprocal amplification of ROS and Ca2+ signals in stressed mdx dystrophic skeletal muscle fibers

Pflügers Archiv, 2009-09, Vol.458 (5), p.915-928

2009

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Type 1 Inositol (1,4,5)-Trisphosphate Receptor Activates Ryanodine Receptor 1 to Mediate Calcium Spark Signaling in Adult Mammalian Skeletal Muscle

The Journal of biological chemistry, 2013-01, Vol.288 (4), p.2103-2109

2013

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Reactive oxygen species contribute to Ca2+ signals produced by osmotic stress in mouse skeletal muscle fibres

The Journal of physiology, 2008-01, Vol.586 (1), p.197-210

2008

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Intestinal Metaplasia of Antral Superficial-foveolar Epithelium in Children with Atrophic Gastritis

The journal of pediatric research, 2017-03, Vol.4 (1), p.6-11

2017

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Mitochondrial redox state and Ca2+ sparks in permeabilized mammalian skeletal muscle

The Journal of physiology, 2005-06, Vol.565 (3), p.855-872

2005

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Metabolic Regulation of Ca2+ Release in Permeabilized Mammalian Skeletal Muscle Fibres

The Journal of physiology, 2003-03, Vol.547 (2), p.453-462

2003

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Local calcium release in mammalian skeletal muscle

The Journal of physiology, 1998-10, Vol.512 (2), p.377-384

1998

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Gαq Sensitizes TRPM8 to Inhibition by PI(4,5)P2 Depletion upon Receptor Activation

The Journal of neuroscience, 2019-07, Vol.39 (31), p.6067-6080

2019

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Pivotal role of miR-448 in the development of ROS-induced cardiomyopathy

Cardiovascular research, 2015-12, Vol.108 (3), p.324-334

2015

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Posttranslational modifications of cardiac ryanodine receptors: Ca(2+) signaling and EC-coupling

Biochimica et biophysica acta, 2013-04, Vol.1833 (4), p.866

2013

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CAVE — SANCTUARY — MYTH: INTERPRETATION CRITERIA FOR THE UPPER PALEOLITHIC DECORATED CAVES IN THE URALS

Uralʹskij istoričeskij vestnik, 2022, Vol.75 (2), p.128-138

2022

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Mitochondrial dysfunctions during progression of dystrophic cardiomyopathy

Cell calcium (Edinburgh), 2015-08, Vol.58 (2), p.186-195

2015

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Abstract 418: Genetic Rescue of Connexin 43 Remodeling in Muscular Dystrophy Cardiomyopathy

Circulation research, 2017-07, Vol.121 (suppl_1)

2017

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Small event Ca2+ release: a probable precursor of Ca2+ sparks in frog skeletal muscle

The Journal of physiology, 1997-07, Vol.502 (Pt 1), p.3-11

1997

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Prevention of connexin-43 remodeling protects against Duchenne muscular dystrophy cardiomyopathy

The Journal of clinical investigation, 2020-04, Vol.130 (4), p.1713-1727

2020

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G αq Sensitizes TRPM8 to Inhibition by PI(4,5)P 2 Depletion upon Receptor Activation

The Journal of neuroscience, 2019-07, Vol.39 (31), p.6067-6080

2019

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Posttranslational modifications of cardiac ryanodine receptors: Ca2+ signaling and EC-coupling

Biochimica et biophysica acta. Molecular cell research, 2013-04, Vol.1833 (4), p.866-875

2013

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Abstract 13964: A Microtubule-Connexin-43 Feed-Forward Loop Suppresses Arrhythmias in Duchenne Muscular Dystrophy Mice

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

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Remodeled connexin 43 hemichannels alter cardiac excitability and promote arrhythmias

The Journal of general physiology, 2023-07, Vol.155 (7)

2023

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Abnormal Sodium Handling and Mitochondrial Metabolism in Cardiac Dystrophy

Biophysical journal, 2011-02, Vol.100 (3), p.81a-81a

2011

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Dystrophic cardiomyopathy: amplification of cellular damage by Ca2+ signalling and reactive oxygen species-generating pathways

Cardiovascular research, 2008-03, Vol.77 (4), p.766-773

2008

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Deficit in PINK1/PARKIN-mediated mitochondrial autophagy at late stages of dystrophic cardiomyopathy

Transfer and Tunneling of Ca2+ from Sarcoplasmic Reticulum to Mitochondria in Skeletal Muscle

Cardiac phenotype of Duchenne Muscular Dystrophy: Insights from cellular studies

Hypersensitivity of excitation-contraction coupling in dystrophic cardiomyocytes

Reciprocal amplification of ROS and Ca2+ signals in stressed mdx dystrophic skeletal muscle fibers

Type 1 Inositol (1,4,5)-Trisphosphate Receptor Activates Ryanodine Receptor 1 to Mediate Calcium Spark Signaling in Adult Mammalian Skeletal Muscle

Reactive oxygen species contribute to Ca2+ signals produced by osmotic stress in mouse skeletal muscle fibres

Intestinal Metaplasia of Antral Superficial-foveolar Epithelium in Children with Atrophic Gastritis

Mitochondrial redox state and Ca2+ sparks in permeabilized mammalian skeletal muscle

Metabolic Regulation of Ca2+ Release in Permeabilized Mammalian Skeletal Muscle Fibres

Local calcium release in mammalian skeletal muscle

Gαq Sensitizes TRPM8 to Inhibition by PI(4,5)P2 Depletion upon Receptor Activation

Pivotal role of miR-448 in the development of ROS-induced cardiomyopathy

Posttranslational modifications of cardiac ryanodine receptors: Ca(2+) signaling and EC-coupling

CAVE — SANCTUARY — MYTH: INTERPRETATION CRITERIA FOR THE UPPER PALEOLITHIC DECORATED CAVES IN THE URALS

Mitochondrial dysfunctions during progression of dystrophic cardiomyopathy

Abstract 418: Genetic Rescue of Connexin 43 Remodeling in Muscular Dystrophy Cardiomyopathy

Small event Ca2+ release: a probable precursor of Ca2+ sparks in frog skeletal muscle

Prevention of connexin-43 remodeling protects against Duchenne muscular dystrophy cardiomyopathy

G αq Sensitizes TRPM8 to Inhibition by PI(4,5)P 2 Depletion upon Receptor Activation

Posttranslational modifications of cardiac ryanodine receptors: Ca2+ signaling and EC-coupling

Abstract 13964: A Microtubule-Connexin-43 Feed-Forward Loop Suppresses Arrhythmias in Duchenne Muscular Dystrophy Mice

Remodeled connexin 43 hemichannels alter cardiac excitability and promote arrhythmias

Abnormal Sodium Handling and Mitochondrial Metabolism in Cardiac Dystrophy

Dystrophic cardiomyopathy: amplification of cellular damage by Ca2+ signalling and reactive oxygen species-generating pathways

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