Results 231 to 240 of about 114,439 (345)

Proteomics of Duchenne Muscular Dystrophy Patient iPSC-Derived Skeletal Muscle Cells Reveal Differential Expression of Cytoskeletal and Extracellular Matrix Proteins. [PDF]

open access: yesCells
Gallert SM   +10 more
europepmc   +1 more source

Exploring the respiratory efficacy of combined chronic glucocorticoid and antioxidant interventions in the mdx mouse: The PREDNAC trial

open access: yesExperimental Physiology, Volume 110, Issue 12, Page 2019-2035, December 1, 2025.
Abstract Duchenne muscular dystrophy (DMD) is characterized by respiratory muscle injury and weakness, ultimately leading to respiratory failure. Impaired respiratory muscle performance, fibrosis and inflammation in early disease are evident in the dystrophin‐deficient mdx mouse model of DMD.
Michael N. Maxwell   +3 more
wiley   +1 more source

Beyond Muscle Weakness: Unraveling Endocrine and Metabolic Dysfunctions in Duchenne Muscular Dystrophy, a Narrative Review [PDF]

open access: gold
Giuseppe Cannalire   +12 more
openalex   +1 more source

Multiomics Analysis of the mdx/mTR Mouse Model of Duchenne Muscular Dystrophy [PDF]

open access: green, 2019
Douglas W. Van Pelt   +9 more
openalex   +1 more source

Weighted cart pull: A novel outcome measure for sustained motor function in mice

open access: yesExperimental Physiology, Volume 110, Issue 12, Page 1978-1989, December 1, 2025.
Abstract Sarcopenia, the pathological age‐related decline in muscle mass and strength, compromises independence and quality of life in older adults. Currently, no effective treatments are available. To enhance translational research using aged mouse models, we developed and validated the weighted cart pull (WCP) as a novel assessment of sustained motor
Charles D. Brennan   +12 more
wiley   +1 more source

Enfermedades genéticas: distrofia muscular de Duchenne

open access: yesRevista de Medicina y Cine / Journal of Medicine and Movies, 2016
María GARCÍA MORO   +2 more
doaj  

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