Muscle strength deficiency and mitochondrial dysfunction in a muscular dystrophy model of Caenorhabditis elegans and its functional response to drugs
出版年份 2018 全文链接
标题
Muscle strength deficiency and mitochondrial dysfunction in a muscular dystrophy model of Caenorhabditis elegans and its functional response to drugs
作者
关键词
-
出版物
Disease Models & Mechanisms
Volume 11, Issue 12, Pages dmm036137
出版商
The Company of Biologists
发表日期
2018-11-05
DOI
10.1242/dmm.036137
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- 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
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now