Search Results - "Uaesoontrachoon, K"
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Eccentric muscle challenge shows osteopontin polymorphism modulation of muscle damage
Published in Human molecular genetics (01-08-2014)“…A promoter polymorphism of the osteopontin (OPN) gene (rs28357094) has been associated with multiple inflammatory states, severity of Duchenne muscular…”
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Protease-activated receptors in the musculoskeletal system
Published in The international journal of biochemistry & cell biology (01-01-2008)“…Protease-activated receptors (PARs) mediate cellular responses to a subset of extracellular proteases, including blood coagulation factors and proteases…”
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P.11.3 Long term treatment with naproxcinod significantly improves skeletal and cardiac function in mdx mouse model of dystrophy
Published in Neuromuscular disorders : NMD (01-10-2013)“…There is evidence that nitric oxide (NO) plays a critical role in skeletal muscle. In Duchenne muscular dystrophy (DMD) patients and the mdx mouse model of…”
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290P Developing a non-invasive, in vivo method for evaluating muscle inflammation longitudinally in two mouse models of Duchenne muscular dystrophy
Published in Neuromuscular disorders : NMD (01-10-2024)“…Muscle inflammation, a key characteristic of Duchenne muscular dystrophy (DMD), is replicated in dystrophin deficient mdx mice, making the model ideal for…”
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P32 Jak inhibitors Tofacitinib and Ruxolitinib do not improve functional deficits in dystrophin-deficient mdx mice
Published in Neuromuscular disorders : NMD (01-10-2023)“…Repurposing FDA approved drugs is a time and cost-effective strategy for finding potential Duchenne muscular dystrophy (DMD) treatments. Janus Kinase (JAK)…”
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DMD – ANIMAL MODELS & PRECLINICAL TREATMENT
Published in Neuromuscular disorders : NMD (01-10-2020)Get full text
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Success of preclinical drug trials using reliable and reproducible endpoints in mouse models of neuromuscular diseases
Published in Neuromuscular disorders : NMD (01-10-2017)Get full text
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P.309 - Success of preclinical drug trials using reliable and reproducible endpoints in mouse models of neuromuscular diseases
Published in Neuromuscular disorders : NMD (01-10-2017)Get full text
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Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophy
Published in Human molecular genetics (15-06-2014)“…In Duchenne muscular dystrophy (DMD) patients and the mouse model of DMD, mdx, dystrophin deficiency causes a decrease and mislocalization of muscle-specific…”
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REGISTRIES AND CARE OF NEUROMUSCULAR DISORDERS
Published in Neuromuscular disorders : NMD (01-10-2018)Get full text
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REGISTRIES AND CARE OF NEUROMUSCULAR DISORDERS: P.297Treatment responsive outcome measures in mouse models of neuromuscular disease
Published in Neuromuscular disorders : NMD (01-10-2018)Get full text
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VBP15, a glucocorticoid analogue, is effective at reducing allergic lung inflammation in mice
Published in PloS one (07-05-2013)“…Asthma is a chronic inflammatory condition of the lower respiratory tract associated with airway hyperreactivity and mucus obstruction in which a majority of…”
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