Abnormal Calcium Handling in Duchenne Muscular Dystrophy: Mechanisms and Potential Therapies
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Abnormal Calcium Handling in Duchenne Muscular Dystrophy: Mechanisms and Potential Therapies
Authors
Keywords
-
Journal
Frontiers in Physiology
Volume 12, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2021-04-09
DOI
10.3389/fphys.2021.647010
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Duchenne muscular dystrophy
- (2021) Dongsheng Duan et al. Nature Reviews Disease Primers
- Prevention of connexin-43 remodeling protects against Duchenne muscular dystrophy cardiomyopathy
- (2020) Eric Himelman et al. JOURNAL OF CLINICAL INVESTIGATION
- Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy
- (2020) Nalinda B. Wasala et al. MOLECULAR THERAPY
- Contribution of TRPC Channels to Intracellular Ca2 + Dyshomeostasis in Smooth Muscle From mdx Mice
- (2020) Jose R. Lopez et al. Frontiers in Physiology
- Small-molecule activation of lysosomal TRP channels ameliorates Duchenne muscular dystrophy in mouse models
- (2020) Lu Yu et al. Science Advances
- Nox4 – RyR1 – Nox2: Regulators of micro-domain signaling in skeletal muscle
- (2020) Tanya R. Cully et al. Redox Biology
- Investigation of the safety and feasibility of AAV1/SERCA2a gene transfer in patients with chronic heart failure supported with a left ventricular assist device – the SERCA-LVAD TRIAL
- (2020) A. R. Lyon et al. GENE THERAPY
- Mitochondrial Dysfunction Is an Early Consequence of Partial or Complete Dystrophin Loss in mdx Mice
- (2020) Timothy M. Moore et al. Frontiers in Physiology
- Gene Therapy With the DWORF Micropeptide Attenuates Cardiomyopathy in Mice
- (2020) Catherine A. Makarewich et al. CIRCULATION RESEARCH
- Sarcolipin haploinsufficiency prevents dystrophic cardiomyopathy in mdx mice
- (2020) Satvik Mareedu et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- NOX5: Molecular biology and pathophysiology
- (2019) Rhian M. Touyz et al. EXPERIMENTAL PHYSIOLOGY
- Crosstalk between Calcium and ROS in Pathophysiological Conditions
- (2019) Simona Feno et al. Oxidative Medicine and Cellular Longevity
- Sarcolipin overexpression impairs myogenic differentiation in Duchenne muscular dystrophy
- (2019) Nandita Niranjan et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- P2X7 purinoceptor as a therapeutic target in muscular dystrophies
- (2019) Dariusz C Górecki CURRENT OPINION IN PHARMACOLOGY
- Mitochondrial dysfunction causes Ca2+ overload and ECM degradation–mediated muscle damage in C. elegans
- (2019) Surabhi Sudevan et al. FASEB JOURNAL
- Targeting RyR activity boosts antisense exon 44 and 45 skipping in human DMD skeletal or cardiac muscle culture models
- (2019) Florian Barthélémy et al. Molecular Therapy-Nucleic Acids
- Blockade of IGF2R improves muscle regeneration and ameliorates Duchenne muscular dystrophy
- (2019) Pamela Bella et al. EMBO Molecular Medicine
- Ca2+ Channels Mediate Bidirectional Signaling between Sarcolemma and Sarcoplasmic Reticulum in Muscle Cells
- (2019) Guillermo Avila et al. Cells
- Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin-deficient mdx mice: proof-of-concept study and independent validation of efficacy
- (2018) Roberta Francesca Capogrosso et al. FASEB JOURNAL
- The relationship between form and function throughout the history of excitation–contraction coupling
- (2018) Clara Franzini-Armstrong JOURNAL OF GENERAL PHYSIOLOGY
- Calcium-induced release of calcium in muscle: 50 years of work and the emerging consensus
- (2018) Eduardo Ríos JOURNAL OF GENERAL PHYSIOLOGY
- Normalization of connexin 43 protein levels prevents cellular and functional signs of dystrophic cardiomyopathy in mice
- (2018) J. Patrick Gonzalez et al. NEUROMUSCULAR DISORDERS
- Mitochondrial Ca 2+ signaling
- (2018) Trayambak Pathak et al. PHARMACOLOGY & THERAPEUTICS
- Physical interaction of junctophilin and the CaV1.1 C terminus is crucial for skeletal muscle contraction
- (2018) Tsutomu Nakada et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Endoplasmic Reticulum–Mitochondrial Contactology: Structure and Signaling Functions
- (2018) György Csordás et al. TRENDS IN CELL BIOLOGY
- The Complex Role of Store Operated Calcium Entry Pathways and Related Proteins in the Function of Cardiac, Skeletal and Vascular Smooth Muscle Cells
- (2018) Javier Avila-Medina et al. Frontiers in Physiology
- Exacerbation of dystrophic cardiomyopathy by phospholamban deficiency-mediated chronically increased cardiac Ca2+ cycling in vivo
- (2018) Michelle L Law et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Truncated dystrophin ameliorates the dystrophic phenotype of mdx mice by reducing sarcolipin-mediated SERCA inhibition
- (2018) Jun Tanihata et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- IP3 receptor blockade restores autophagy and mitochondrial function in skeletal muscle fibers of dystrophic mice
- (2018) Denisse Valladares et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Necroptosis mediates myofibre death in dystrophin-deficient mice
- (2018) Jennifer E. Morgan et al. Nature Communications
- Mitochondrial Permeability Transition: A Molecular Lesion with Multiple Drug Targets
- (2018) Thomas Briston et al. TRENDS IN PHARMACOLOGICAL SCIENCES
- Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle
- (2018) John T. Olthoff et al. Nature Communications
- The DWORF micropeptide enhances contractility and prevents heart failure in a mouse model of dilated cardiomyopathy
- (2018) Catherine A Makarewich et al. eLife
- Duchenne muscular dystrophy: Focus on arachidonic acid metabolites
- (2018) Malvina Hoxha BIOMEDICINE & PHARMACOTHERAPY
- Intracellular calcium release channels: an update
- (2017) Gaetano Santulli et al. JOURNAL OF PHYSIOLOGY-LONDON
- Alisporivir rescues defective mitochondrial respiration in Duchenne muscular dystrophy
- (2017) Marco Schiavone et al. PHARMACOLOGICAL RESEARCH
- Reducing sarcolipin expression mitigates Duchenne muscular dystrophy and associated cardiomyopathy in mice
- (2017) Antanina Voit et al. Nature Communications
- Molecular mechanisms of STIM/Orai communication
- (2016) Isabella Derler et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis
- (2016) Luis A. Cea et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- Inositol 1,4,5-trisphosphate (IP3)-dependent Ca2+signaling mediates delayed myogenesis in Duchenne muscular dystrophy fetal muscle
- (2016) Andrea Farini et al. DEVELOPMENT
- The importance of genetic diagnosis for Duchenne muscular dystrophy
- (2016) Annemieke Aartsma-Rus et al. JOURNAL OF MEDICAL GENETICS
- Phospholamban and sarcolipin: Are they functionally redundant or distinct regulators of the Sarco(Endo)Plasmic Reticulum Calcium ATPase?
- (2016) Sana A. Shaikh et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Eliminating Nox2 reactive oxygen species production protects dystrophic skeletal muscle from pathological calcium influx assessedin vivoby manganese-enhanced magnetic resonance imaging
- (2016) James A. Loehr et al. JOURNAL OF PHYSIOLOGY-LONDON
- Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy
- (2016) David G. Allen et al. PHYSIOLOGICAL REVIEWS
- A peptide encoded by a transcript annotated as long noncoding RNA enhances SERCA activity in muscle
- (2016) B. R. Nelson et al. SCIENCE
- Anti-inflammatory drugs for Duchenne muscular dystrophy: focus on skeletal muscle-releasing factors
- (2016) Yoshitsugu Aoki et al. Drug Design Development and Therapy
- Pharmacological therapeutics targeting the secondary defects and downstream pathology of Duchenne muscular dystrophy
- (2016) Janelle M. Spinazzola et al. Expert Opinion on Orphan Drugs
- SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models
- (2015) Davi A. G. Mázala et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Pivotal role of miR-448 in the development of ROS-induced cardiomyopathy
- (2015) Sergii Kyrychenko et al. CARDIOVASCULAR RESEARCH
- A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance
- (2015) Douglas M. Anderson et al. CELL
- Mitochondrial dysfunctions during progression of dystrophic cardiomyopathy
- (2015) Victoria Kyrychenko et al. CELL CALCIUM
- Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy
- (2015) A R Burr et al. CELL DEATH AND DIFFERENTIATION
- Physiological and Pathological Roles of the Mitochondrial Permeability Transition Pore in the Heart
- (2015) Jennifer Q. Kwong et al. Cell Metabolism
- The Ins and Outs of Mitochondrial Calcium
- (2015) T. Finkel et al. CIRCULATION RESEARCH
- Ca2+-Dependent Regulations and Signaling in Skeletal Muscle: From Electro-Mechanical Coupling to Adaptation
- (2015) Sebastian Gehlert et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Crosstalk between RyR2 oxidation and phosphorylation contributes to cardiac dysfunction in mice with Duchenne muscular dystrophy
- (2015) Qiongling Wang et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Signaling in Muscle Contraction
- (2015) Ivana Y. Kuo et al. Cold Spring Harbor Perspectives in Biology
- Small-molecule activation of SERCA2a SUMOylation for the treatment of heart failure
- (2015) Changwon Kho et al. Nature Communications
- Duchenne Muscular Dystrophy Gene Therapy in the Canine Model
- (2015) Dongsheng Duan Human Gene Therapy Clinical Development
- Calcium and ROS: A mutual interplay
- (2015) Agnes Görlach et al. Redox Biology
- Membrane-stabilizing copolymers confer marked protection to dystrophic skeletal muscle in vivo
- (2015) Evelyne M Houang et al. Molecular Therapy-Methods & Clinical Development
- Metabolic Dysfunction and Altered Mitochondrial Dynamics in the Utrophin-Dystrophin Deficient Mouse Model of Duchenne Muscular Dystrophy
- (2015) Meghna Pant et al. PLoS One
- Chronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin-/- Mice
- (2015) Bruce E. Markham et al. PLoS One
- Impaired structural and functional regeneration of skeletal muscles fromβ2-adrenoceptor knockout mice
- (2014) M. T. Silva et al. Acta Physiologica
- NADPH oxidase-2 inhibition restores contractility and intracellular calcium handling and reduces arrhythmogenicity in dystrophic cardiomyopathy
- (2014) Daniel R. Gonzalez et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Store-operated Ca2+entry in muscle physiology and diseases
- (2014) Zui Pan et al. BMB Reports
- Na+ Dysregulation Coupled with Ca2+ Entry through NCX1 Promotes Muscular Dystrophy in Mice
- (2014) A. R. Burr et al. MOLECULAR AND CELLULAR BIOLOGY
- The intracellular Ca2+ channel MCOLN1 is required for sarcolemma repair to prevent muscular dystrophy
- (2014) Xiping Cheng et al. NATURE MEDICINE
- Membrane Injury and Repair in the Muscular Dystrophies
- (2014) Sandra T. Cooper et al. NEUROSCIENTIST
- Poloxomer 188 Has a Deleterious Effect on Dystrophic Skeletal Muscle Function
- (2014) Rebecca L. Terry et al. PLoS One
- Functional β-Adrenoceptors Are Important for Early Muscle Regeneration in Mice through Effects on Myoblast Proliferation and Differentiation
- (2014) Jarrod E. Church et al. PLoS One
- Defects in Mitochondrial ATP Synthesis in Dystrophin-Deficient Mdx Skeletal Muscles May Be Caused by Complex I Insufficiency
- (2014) Emma Rybalka et al. PLoS One
- Diapocynin, a Dimer of the NADPH Oxidase Inhibitor Apocynin, Reduces ROS Production and Prevents Force Loss in Eccentrically Contracting Dystrophic Muscle
- (2014) Hesham M. Ismail et al. PLoS One
- Phospholipid Synthesis and Transport in Mammalian Cells
- (2014) Jean E. Vance TRAFFIC
- Damage control: cellular mechanisms of plasma membrane repair
- (2014) Norma W. Andrews et al. TRENDS IN CELL BIOLOGY
- Src-dependent impairment of autophagy by oxidative stress in a mouse model of Duchenne muscular dystrophy
- (2014) Rituraj Pal et al. Nature Communications
- L-type Ca2+ channel contributes to alterations in mitochondrial calcium handling in the mdx ventricular myocyte
- (2013) Helena M. Viola et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Enhanced currents through L-type calcium channels in cardiomyocytes disturb the electrophysiology of the dystrophic heart
- (2013) Xaver Koenig et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Long-Term Effects of AAV1/SERCA2a Gene Transfer in Patients With Severe Heart Failure
- (2013) Krisztina Zsebo et al. CIRCULATION RESEARCH
- Impairment of calcium ATPases by high glucose and potential pharmacological protection
- (2013) L. Horáková et al. FREE RADICAL RESEARCH
- Increased sarcolipin expression and decreased sarco(endo)plasmic reticulum Ca2+ uptake in skeletal muscles of mouse models of Duchenne muscular dystrophy
- (2013) Joel S. Schneider et al. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
- Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy
- (2013) Jerry R. Mendell et al. MUSCLE & NERVE
- Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
- (2013) Anne M. Connolly et al. NEUROMUSCULAR DISORDERS
- Nifedipine Treatment Reduces Resting Calcium Concentration, Oxidative and Apoptotic Gene Expression, and Improves Muscle Function in Dystrophic mdx Mice
- (2013) Francisco Altamirano et al. PLoS One
- Mitochondrial calcium uptake
- (2013) G. S. B. Williams et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Lipid Transport between the Endoplasmic Reticulum and Mitochondria
- (2013) V. V. Flis et al. Cold Spring Harbor Perspectives in Biology
- Where the endoplasmic reticulum and the mitochondrion tie the knot: The mitochondria-associated membrane (MAM)
- (2012) Arun Raturi et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- Mitofusin 2-Containing Mitochondrial-Reticular Microdomains Direct Rapid Cardiomyocyte Bioenergetic Responses Via Interorganelle Ca 2+ Crosstalk
- (2012) Yun Chen et al. CIRCULATION RESEARCH
- Modulation of Cardiac Contractility by the Phopholamban/SERCA2a Regulatome
- (2012) Evangelia G. Kranias et al. CIRCULATION RESEARCH
- Sarcoplasmic reticulum Ca2+permeation explored from the lumen side inmdxmuscle fibers under voltage control
- (2012) Gaëlle Robin et al. JOURNAL OF GENERAL PHYSIOLOGY
- Connexin- and Pannexin-Based Channels in Normal Skeletal Muscles and Their Possible Role in Muscle Atrophy
- (2012) Luis A. Cea et al. JOURNAL OF MEMBRANE BIOLOGY
- Cardiac phenotype of Duchenne Muscular Dystrophy: Insights from cellular studies
- (2012) Natalia Shirokova et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Contribution of oxidative stress to pathology in diaphragm and limb muscles with Duchenne muscular dystrophy
- (2012) Jong-Hee Kim et al. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
- Hsp72 preserves muscle function and slows progression of severe muscular dystrophy
- (2012) Stefan M. Gehrig et al. NATURE
- Chronic Administration of a Leupeptin-Derived Calpain Inhibitor Fails to Ameliorate Severe Muscle Pathology in a Canine Model of Duchenne Muscular Dystrophy
- (2012) Martin K. Childers et al. Frontiers in Pharmacology
- The Effect of Enalapril and Carvedilol on Left Ventricular Dysfunction in Middle Childhood and Adolescent Patients With Muscular Dystrophy
- (2012) Hye Won Kwon et al. Korean Circulation Journal
- Long-Term Blocking of Calcium Channels in mdx Mice Results in Differential Effects on Heart and Skeletal Muscle
- (2011) Louise H. Jørgensen et al. AMERICAN JOURNAL OF PATHOLOGY
- Stretch-activated calcium channel protein TRPC1 is correlated with the different degrees of the dystrophic phenotype in mdx mice
- (2011) Cíntia Yuri Matsumura et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Alignment of sarcoplasmic reticulum-mitochondrial junctions with mitochondrial contact points
- (2011) Cecília García-Pérez et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Sarcalumenin plays a critical role in age-related cardiac dysfunction due to decreases in SERCA2a expression and activity
- (2011) Qibin Jiao et al. CELL CALCIUM
- Calcium signaling around Mitochondria Associated Membranes (MAMs)
- (2011) Simone Patergnani et al. Cell Communication and Signaling
- The role of branched fibres in the pathogenesis of Duchenne muscular dystrophy
- (2011) S. Chan et al. EXPERIMENTAL PHYSIOLOGY
- P2X7 purinoceptor alterations in dystrophic mdx mouse muscles: relationship to pathology and potential target for treatment
- (2011) Christopher N. J. Young et al. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
- Mitigation of muscular dystrophy in mice by SERCA overexpression in skeletal muscle
- (2011) Sanjeewa A. Goonasekera et al. JOURNAL OF CLINICAL INVESTIGATION
- SERCA2a gene transfer improves electrocardiographic performance in aged mdx mice
- (2011) Jin-Hong Shin et al. Journal of Translational Medicine
- X-ROS Signaling: Rapid Mechano-Chemo Transduction in Heart
- (2011) B. L. Prosser et al. SCIENCE
- Excitation-contraction coupling alterations in mdx and utrophin/dystrophin double knockout mice: a comparative study
- (2010) Joana Capote et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Upregulation of store-operated Ca2+ entry in dystrophic mdx mouse muscle
- (2010) Joshua N. Edwards et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Leupeptin-based inhibitors do not improve the mdx phenotype
- (2010) Joshua Selsby et al. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
- Short Communication: Oxidative Posttranslational Modifications Mediate Decreased SERCA Activity and Myocyte Dysfunction in Gαq-Overexpressing Mice
- (2010) Steve Lancel et al. CIRCULATION RESEARCH
- Branched fibres in old dystrophicmdxmuscle are associated with mechanical weakening of the sarcolemma, abnormal Ca2+transients and a breakdown of Ca2+homeostasis during fatigue
- (2010) Stewart I. Head EXPERIMENTAL PHYSIOLOGY
- Overexpression of SERCA1a in the mdx Diaphragm Reduces Susceptibility to Contraction-Induced Damage
- (2010) Kevin J. Morine et al. HUMAN GENE THERAPY
- Duchenne muscular dystrophy – What causes the increased membrane permeability in skeletal muscle?
- (2010) David G. Allen et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs
- (2010) DeWayne Townsend et al. JOURNAL OF CLINICAL INVESTIGATION
- Histidine-rich calcium binding protein: The new regulator of sarcoplasmic reticulum calcium cycling
- (2010) Demetrios A. Arvanitis et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Treatment of Duchenne muscular dystrophy with ciclosporin A: a randomised, double-blind, placebo-controlled multicentre trial
- (2010) Janbernd Kirschner et al. LANCET NEUROLOGY
- Leaky RyR2 trigger ventricular arrhythmias in Duchenne muscular dystrophy
- (2010) J. Fauconnier et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Ca2+ channels and skeletal muscle diseases
- (2010) Eun Hui Lee PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY
- Ryanodine Receptors: Structure, Expression, Molecular Details, and Function in Calcium Release
- (2010) J. T. Lanner et al. Cold Spring Harbor Perspectives in Biology
- Negative modulation of inositol 1,4,5-trisphosphate type 1 receptor expression prevents dystrophin-deficient muscle cells death
- (2009) Ludivine Mondin et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Ryanodine receptor Ca2+ sensitivity and excitation-contraction coupling in muscular dystrophy and heart failure: similar and yet different
- (2009) Thomas R. Shannon AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Phospholipase A2-derived lysophosphatidylcholine triggers Ca2+ entry in dystrophic skeletal muscle fibers
- (2009) François-Xavier Boittin et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions
- (2009) Nadège Zanou et al. FEBS LETTERS
- Calcium-binding proteins in skeletal muscles of the mdx mice: potential role in the pathogenesis of Duchenne muscular dystrophy
- (2009) Adriana Pertille et al. INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY
- Regulation of TRPC1 and TRPC4 Cation Channels Requires an α1-Syntrophin-dependent Complex in Skeletal Mouse Myotubes
- (2009) Jessica Sabourin et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
- (2009) Katharine Bushby et al. LANCET NEUROLOGY
- Sarcoplasmic-endoplasmic-reticulum Ca2+-ATPase and calsequestrin are overexpressed in spared intrinsic laryngeal muscles of dystrophin-deficientmdxmice
- (2009) Renato Ferretti et al. MUSCLE & NERVE
- Diltiazem and verapamil protect dystrophin-deficient muscle fibers ofMDXmice from degeneration: A potential role in calcium buffering and sarcolemmal stability
- (2009) Cintia Yuri Matsumura et al. MUSCLE & NERVE
- Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle
- (2009) Andrew M Bellinger et al. NATURE MEDICINE
- Calcium-Induced Calcium Release in Skeletal Muscle
- (2009) Makoto Endo PHYSIOLOGICAL REVIEWS
- Investigation of Debio 025, a cyclophilin inhibitor, in the dystrophic mdx mouse, a model for Duchenne muscular dystrophy
- (2008) J Reutenauer et al. BRITISH JOURNAL OF PHARMACOLOGY
- Dominant-negative inhibition of Ca2+ influx via TRPV2 ameliorates muscular dystrophy in animal models
- (2008) Yuko Iwata et al. HUMAN MOLECULAR GENETICS
- Physical Coupling Supports the Local Ca2+Transfer between Sarcoplasmic Reticulum Subdomains and the Mitochondria in Heart Muscle
- (2008) Cecilia García-Pérez et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- TRPC1 binds to caveolin-3 and is regulated by Src kinase - role in Duchenne muscular dystrophy
- (2008) O. L. Gervasio et al. JOURNAL OF CELL SCIENCE
- Nav1.4 Deregulation in Dystrophic Skeletal Muscle Leads to Na+Overload and Enhanced Cell Death
- (2008) Carole Hirn et al. JOURNAL OF GENERAL PHYSIOLOGY
- Calsequestrin content and SERCA determine normal and maximal Ca2+storage levels in sarcoplasmic reticulum of fast- and slow-twitch fibres of rat
- (2008) Robyn M. Murphy et al. JOURNAL OF PHYSIOLOGY-LONDON
- Mitofusin 2 tethers endoplasmic reticulum to mitochondria
- (2008) Olga Martins de Brito et al. NATURE
- Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy
- (2008) Douglas P Millay et al. NATURE MEDICINE
- Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy
- (2008) Miranda D. Grounds et al. NEUROBIOLOGY OF DISEASE
- Dystrophin-deficient cardiomyopathy in mouse: Expression of Nox4 and Lox are associated with fibrosis and altered functional parameters in the heart
- (2008) Christopher F. Spurney et al. NEUROMUSCULAR DISORDERS
- L-Type Ca2+ Channel Function Is Linked to Dystrophin Expression in Mammalian Muscle
- (2008) Oliver Friedrich et al. PLoS One
- Dystrophic skeletal muscle fibers display alterations at the level of calcium microdomains
- (2008) M. DiFranco et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started