Muscle strength deficiency and mitochondrial dysfunction in a muscular dystrophy model of Caenorhabditis elegans and its functional response to drugs

NemaFlex: a microfluidics-based technology for standardized measurement of muscular strength of C. elegans

(2018) Mizanur Rahman et al.   LAB ON A CHIP

DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants

(2018) Charlotte Scholtes et al.   Scientific Reports

A screening-based platform for the assessment of cellular respiration in Caenorhabditis elegans

(2016) Mandy Koopman et al.   Nature Protocols

An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments

(2015) Zhichang Qiu et al.   Biomicrofluidics

Colored polydimethylsiloxane micropillar arrays for high throughput measurements of forces applied by genetic model organisms

(2015) Siddharth M. Khare et al.   Biomicrofluidics

Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies

(2015) Elisabeth Le Rumeur   Bosnian Journal of Basic Medical Sciences

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

(2015) J. W. McGreevy et al.   Disease Models & Mechanisms

The integrin-adhesome is required to maintain muscle structure, mitochondrial ATP production, and movement forces in Caenorhabditis elegans

(2015) Timothy Etheridge et al.   FASEB JOURNAL

The burrowing behavior of the nematodeCaenorhabditis elegans: a new assay for the study of neuromuscular disorders

(2015) C. Beron et al.   GENES BRAIN AND BEHAVIOR

Ultra-structural time-course study in theC. elegansmodel for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process

(2015) Nicolas Brouilly et al.   HUMAN MOLECULAR GENETICS

Degenerin channel activation causes caspase-mediated protein degradation and mitochondrial dysfunction in adultC. elegansmuscle

(2015) Christopher J. Gaffney et al.   Journal of Cachexia Sarcopenia and Muscle

In vivo single-molecule imaging identifies altered dynamics of calcium channels in dystrophin-mutant C. elegans

(2014) Hong Zhan et al.   Nature Communications

Automated, high-throughput, motility analysis in Caenorhabditis elegans and parasitic nematodes: Applications in the search for new anthelmintics

(2014) Steven D. Buckingham et al.   International Journal for Parasitology-Drugs and Drug Resistance

Methods to Assess Subcellular Compartments of Muscle in C. elegans

(2014) Christopher J. Gaffney et al.   Jove-Journal of Visualized Experiments

WormFarm: a quantitative control and measurement device toward automatedCaenorhabditis elegansaging analysis

(2013) Bo Xian et al.   AGING CELL

Probing the anti-aging role of polydatin in Caenorhabditis elegans on a chip

(2013) Hui Wen et al.   Integrative Biology

On-chip analysis of C. elegans muscular forces and locomotion patterns in microstructured environments

(2013) Shazlina Johari et al.   LAB ON A CHIP

Reduced IGF signaling prevents muscle cell death in a Caenorhabditis elegans model of muscular dystrophy

(2013) K. H. Oh et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Multiparameter evaluation of the longevity in C. elegans under stress using an integrated microfluidic device

(2012) Hui Wen et al.   BIOMEDICAL MICRODEVICES

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures

(2012) Alberto Lerario et al.   BMC Neurology

Emerging drugs for Duchenne muscular dystrophy

(2012) Vinod Malik et al.   EXPERT OPINION ON EMERGING DRUGS

A micropillar-based on-chip system for continuous force measurement ofC. elegans

(2012) Ali Ghanbari et al.   JOURNAL OF MICROMECHANICS AND MICROENGINEERING

Melatonin treatment counteracts the hyperoxidative status in erythrocytes of patients suffering from Duchenne muscular dystrophy

(2011) Mariam Chahbouni et al.   CLINICAL BIOCHEMISTRY

Melatonin improves muscle function of the dystrophic mdx5Cv mouse, a model for Duchenne muscular dystrophy

(2011) Youssef Hibaoui et al.   JOURNAL OF PINEAL RESEARCH

Melatonin treatment normalizes plasma pro-inflammatory cytokines and nitrosative/oxidative stress in patients suffering from Duchenne muscular dystrophy

(2010) Mariam Chahbouni et al.   JOURNAL OF PINEAL RESEARCH

Loss of dystrophin and the microtubule-binding protein ELP-1 causes progressive paralysis and death of adultC. elegans

(2009) Jennifer L. Hueston et al.   DEVELOPMENTAL DYNAMICS

Lifespan-on-a-chip: microfluidic chambers for performing lifelong observation of C. elegans

(2009) S. Elizabeth Hulme et al.   LAB ON A CHIP

Collapse of proteostasis represents an early molecular event in Caenorhabditis elegans aging

(2009) A. Ben-Zvi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA