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Published in 2021 at "Journal of Leukocyte Biology"
DOI: 10.1002/jlb.3a0920-620r
Abstract: No longer regarded simply as end‐stage cytotoxic effectors, eosinophils are now recognized as complex cells with unique phenotypes that develop in response stimuli in the local microenvironment. In our previous study, we documented eosinophil infiltration…
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Keywords:
expression;
mice;
muscle;
mdx ... See more keywords
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Published in 2018 at "Molecular Neurobiology"
DOI: 10.1007/s12035-018-1018-8
Abstract: We have previously shown that inadequate dystrophin in cortical neurons in mdx mice is associated with age-dependent dyshomeostasis of resting intracellular Ca2+ ([Ca2+]i) and Na+ ([Na+]i), elevated reactive oxygen species (ROS) production, increase in neuronal…
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Keywords:
body periodic;
mdx neurons;
mdx;
nitric oxide ... See more keywords
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Published in 2017 at "Journal of Cell Communication and Signaling"
DOI: 10.1007/s12079-017-0439-x
Abstract: The Kallikrein Kinin System (KKS) is a vasoactive peptide system with known functions in the maintenance of tissue homeostasis, renal function and blood pressure. The main effector peptide of KKS is Bradykinin (BK). This ligand…
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Keywords:
receptors worsens;
worsens dystrophic;
mdx mice;
mdx ... See more keywords
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Published in 2020 at "EBioMedicine"
DOI: 10.1016/j.ebiom.2020.102700
Abstract: Background Duchenne muscular dystrophy (DMD) is caused by the loss of dystrophin. Severe and ultimately lethal, DMD progresses relatively slowly in that patients become wheelchair bound only around age twelve with a survival expectancy reaching…
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Keywords:
mdx mice;
muscular dystrophy;
stress;
mdx ... See more keywords
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Published in 2019 at "Scientific Reports"
DOI: 10.1038/s41598-019-48744-7
Abstract: Duchenne muscular dystrophy (DMD) is a uniformly fatal condition of striated muscle wasting resulting in premature death from respiratory and/or cardiac failure. Symptomatic therapy has prolonged survival by limiting deaths resulting from respiratory insufficiency, but…
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Keywords:
therapy;
muscle;
function;
mdx ... See more keywords
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2
Published in 2023 at "Europace"
DOI: 10.1093/europace/euad122.592
Abstract: Abstract Funding Acknowledgements Type of funding sources: None. Background The cardiac sodium channel Nav1.5 is transported to the membrane by the microtubule network. Alterations in microtubule dynamics are known to impact on ion channel trafficking.…
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Keywords:
microtubule detyrosination;
parthenolide;
mdx;
cms ... See more keywords
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Published in 2022 at "International Journal of Experimental Pathology"
DOI: 10.1111/iep.12461
Abstract: Duchenne muscular dystrophy (DMD) is the most severe and frequent form of muscular dystrophy. The mdx mouse is one of the most widely used experimental models to understand aspects of the biology of dystrophic skeletal…
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Keywords:
mdx mice;
mdx;
oxidative stress;
muscle ... See more keywords
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Published in 2023 at "Physiology"
DOI: 10.1152/physiol.2023.38.s1.5730580
Abstract: Background: Duchenne muscular dystrophy (DMD) is an X-linked recessive muscle wasting disease that, with no cure, leads to early mortality (30-40 years of age). Previous studies have shown that voluntary wheel running can mitigate disease…
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Keywords:
serca function;
mdx;
muscle;
physiology ... See more keywords
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Published in 2018 at "Oxidative Medicine and Cellular Longevity"
DOI: 10.1155/2018/4814696
Abstract: Duchenne muscular dystrophy (DMD) is a genetic disease associated with mutations of Dystrophin gene that regulate myofiber integrity and muscle degeneration, characterized by oxidative stress increase. We previously published that reactive oxygen species (ROS) induce…
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Keywords:
skeletal muscle;
myogenic differentiation;
muscle;
mdx ... See more keywords
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Published in 2020 at "JCI insight"
DOI: 10.1172/jci.insight.135703
Abstract: Duchenne muscular dystrophy (DMD) is a chronic muscle disease characterized by poor myogenesis and replacement of muscle by extracellular matrix. Despite the shared genetic basis, severity of these deficits varies among patients. One source of…
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Keywords:
muscle;
disease;
tgf;
muscle degeneration ... See more keywords
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Published in 2021 at "BMC Cardiovascular Disorders"
DOI: 10.1186/s12872-021-02112-4
Abstract: Background Duchenne muscular dystrophy (DMD) associated cardiomyopathy is a major cause of morbidity and mortality. In an in vitro DMD cardiomyocyte model, nicorandil reversed stress-induced cell injury through multiple pathways implicated in DMD . We…
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Keywords:
dmd;
isoproterenol;
nicorandil isoproterenol;
isoproterenol induced ... See more keywords