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Exercise exacerbates decline in the musculature of an animal model of Duchenne muscular dystrophy

https://doi.org/10.1101/360388
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inferredcites →https://doi.org/10.1002/0471142727.mb2603s109openalex-snapshot
RNA Interference in Caenorhabditis elegans
inferredcites →https://doi.org/10.1002/mus.23244openalex-snapshot
Exercise and duchenne muscular dystrophy: Where we have been and where we need to go
inferredcites →https://doi.org/10.1002/mus.25111openalex-snapshot
The muscular dystrophy coordinating committee action plan for the muscular dystrophies
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-1-4612-4380-9_25openalex-snapshot
Nonparametric Estimation from Incomplete Observations
inferredcites →https://doi.org/10.1007/978-1-4612-4380-9_37openalex-snapshot
Regression Models and Life-Tables
inferredcites →https://doi.org/10.1007/bf00687043openalex-snapshot
Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse
inferredcites →https://doi.org/10.1007/bf02034655openalex-snapshot
Role of intracellular calcium in promoting muscle damage: A strategy for controlling the dystrophic condition
inferredcites →https://doi.org/10.1016/0022-510x(92)90023-eopenalex-snapshot
Increased leakage of calcium ion from the sarcoplasmic reticulum of the mdx mouse
inferredcites →https://doi.org/10.1016/0092-8674(87)90504-6openalex-snapshot
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
inferredcites →https://doi.org/10.1016/0092-8674(87)90579-4openalex-snapshot
Dystrophin: The protein product of the duchenne muscular dystrophy locus
inferredcites →https://doi.org/10.1016/0143-4160(95)90062-4openalex-snapshot
Abnormal calcium homeostasis in Duchenne muscular dystrophy myotubes contracting in vitro
inferredcites →https://doi.org/10.1016/j.bbapap.2010.05.001openalex-snapshot
Dystrophin: More than just the sum of its parts
inferredcites →https://doi.org/10.1016/j.jneumeth.2016.02.023openalex-snapshot
Method for the assessment of neuromuscular integrity and burrowing choice in vermiform animals
inferredcites →https://doi.org/10.1016/j.jpeds.2006.12.045openalex-snapshot
Delayed Developmental Language Milestones in Children with Duchenne’s Muscular Dystrophy
inferredcites →https://doi.org/10.1016/s0014-5793(99)01651-8openalex-snapshot
Mutations in the dystrophin‐like dys‐1 gene of Caenorhabditis elegans result in reduced acetylcholinesterase activity
inferredcites →https://doi.org/10.1016/s0092-8674(00)80532-2openalex-snapshot
Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy
inferredcites →https://doi.org/10.1016/s0960-8966(02)00140-2openalex-snapshot
Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation
inferredcites →https://doi.org/10.1016/s0960-8966(99)00011-5openalex-snapshot
Molecular analysis of a spontaneous dystrophin `knockout' dog
inferredcites →https://doi.org/10.1016/s0960-9822(00)00691-6openalex-snapshot
Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0960-9822(01)00528-0openalex-snapshot
Muscular degeneration in the absence of dystrophin is a calcium-dependent process
inferredcites →https://doi.org/10.1016/s1474-4422(09)70271-6openalex-snapshot
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
inferredcites →https://doi.org/10.1017/erm.2014.17openalex-snapshot
Dysregulation of calcium homeostasis in muscular dystrophies
inferredcites →https://doi.org/10.1017/s003358351000017xopenalex-snapshot
The sarcoplasmic Ca2+-ATPase: design of a perfect chemi-osmotic pump
inferredcites →https://doi.org/10.1038/323646a0openalex-snapshot
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene
inferredcites →https://doi.org/10.1038/cdd.2016.127openalex-snapshot
Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy
inferredcites →https://doi.org/10.1038/labinvest.2010.146openalex-snapshot
An intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breed
inferredcites →https://doi.org/10.1038/nature02798openalex-snapshot
SNF-6 is an acetylcholine transporter interacting with the dystrophin complex in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nrm2024openalex-snapshot
Molecular mechanisms of muscular dystrophies: old and new players
inferredcites →https://doi.org/10.1046/j.1365-201x.2001.00839.xopenalex-snapshot
Muscle training in muscular dystrophies
inferredcites →https://doi.org/10.1051/medsci/20031967725openalex-snapshot
C. elegans : des neurones et des gènes
inferredcites →https://doi.org/10.1073/pnas.0810359105openalex-snapshot
Genetic analysis of crawling and swimming locomotory patterns in C. elegans
inferredcites →https://doi.org/10.1073/pnas.0906591106openalex-snapshot
Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism
inferredcites →https://doi.org/10.1073/pnas.1108673108openalex-snapshot
Caenorhabditis elegans selects distinct crawling and swimming gaits via dopamine and serotonin
inferredcites →https://doi.org/10.1073/pnas.90.8.3710openalex-snapshot
Dystrophin protects the sarcolemma from stresses developed during muscle contraction.
inferredcites →https://doi.org/10.1083/jcb.152.6.1313openalex-snapshot
The Caenorhabditis elegans unc-78 Gene Encodes a Homologue of Actin-Interacting Protein 1 Required for Organized Assembly of Muscle Actin Filaments
inferredcites →https://doi.org/10.1085/jgp.201010436openalex-snapshot
Mechanisms of muscle weakness in muscular dystrophy
inferredcites →https://doi.org/10.1093/emboj/cdf681openalex-snapshot
Physiological calcium concentrations regulate calmodulin binding and catalysis of adenylyl cyclase exotoxins
inferredcites →https://doi.org/10.1093/genetics/77.1.71openalex-snapshot
THE GENETICS OF CAENORHABDITIS ELEGANS
inferredcites →https://doi.org/10.1093/hmg/ddl065openalex-snapshot
Targeted inhibition of Ca2+/calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle
inferredcites →https://doi.org/10.1093/qjmed/hci113openalex-snapshot
Analysis of an adult Duchenne muscular dystrophy population
inferredcites →https://doi.org/10.1097/00002060-200212000-00004openalex-snapshot
Predictive Factors of Cessation of Ambulation in Patients with Duchenne Muscular Dystrophy
inferredcites →https://doi.org/10.1111/gbb.12217openalex-snapshot
The burrowing behavior of the nematode Caenorhabditis elegans: a new assay for the study of neuromuscular disorders
inferredcites →https://doi.org/10.1111/j.1365-2613.2009.00688.xopenalex-snapshot
Calcium‐binding proteins in skeletal muscles of the mdx mice: potential role in the pathogenesis of Duchenne muscular dystrophy
inferredcites →https://doi.org/10.1111/j.2517-6161.1972.tb00899.xopenalex-snapshot
Regression Models and Life-Tables
inferredcites →https://doi.org/10.1177/1049909109346165openalex-snapshot
Pain in Youths With Neuromuscular Disease
inferredcites →https://doi.org/10.1186/1471-2199-9-9openalex-snapshot
Selection and validation of a set of reliable reference genes for quantitative sod gene expression analysis in C. elegans
inferredcites →https://doi.org/10.1186/s12915-017-0368-4openalex-snapshot
Single swim sessions in C. elegans induce key features of mammalian exercise
inferredcites →https://doi.org/10.1242/dmm.018424openalex-snapshot
Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy
inferredcites →https://doi.org/10.1242/jcs.02814openalex-snapshot
Dystroglycan: from biosynthesis to pathogenesis of human disease
inferredcites →https://doi.org/10.1242/jcs.115.14.2801openalex-snapshot
The dystrophin-associated protein complex
inferredcites →https://doi.org/10.1249/01.jes.0000240020.84630.9dopenalex-snapshot
Recommendations to Define Exercise Prescription for Duchenne Muscular Dystrophy
inferredcites →https://doi.org/10.1371/journal.pone.0002418openalex-snapshot
Genetic Modifier Screens Reveal New Components that Interact with the Drosophila Dystroglycan-Dystrophin Complex
inferredcites →https://doi.org/10.1371/journal.pone.0065414openalex-snapshot
Efficacy of Muscle Exercise in Patients with Muscular Dystrophy: A Systematic Review Showing a Missed Opportunity to Improve Outcomes
inferredcites →https://doi.org/10.2307/2281868openalex-snapshot
Nonparametric Estimation from Incomplete Observations
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