scholarly article | Q13442814 |
P50 | author | Jean-Francois Rolland | Q58227354 |
Annamaria De Luca | Q42518905 | ||
P2093 | author name string | S Simonetti | |
B Nico | |||
V Longo | |||
A Cozzoli | |||
R F Capogrosso | |||
V T Sblendorio | |||
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Alteration of excitation-contraction coupling mechanism in extensor digitorum longus muscle fibres of dystrophic mdx mouse and potential efficacy of taurine | Q28354192 | ||
IRES-mediated translation of utrophin A is enhanced by glucocorticoid treatment in skeletal muscle cells | Q28472887 | ||
How calcium influx through calcium leak channels is responsible for the elevated levels of calcium-dependent proteolysis in dystrophic myotubes | Q34204770 | ||
Molecular pathophysiology and targeted therapeutics for muscular dystrophy | Q34360418 | ||
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A multidisciplinary evaluation of the effectiveness of cyclosporine a in dystrophic mdx mice. | Q35083651 | ||
Lipid peroxidation inhibition blunts nuclear factor-kappaB activation, reduces skeletal muscle degeneration, and enhances muscle function in mdx mice. | Q35087995 | ||
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Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy | Q36841572 | ||
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New therapies for Duchenne muscular dystrophy: challenges, prospects and clinical trials. | Q36993575 | ||
Shifts in macrophage phenotypes and macrophage competition for arginine metabolism affect the severity of muscle pathology in muscular dystrophy | Q37090043 | ||
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Bcl-2 overexpression prevents calcium overload and subsequent apoptosis in dystrophic myotubes | Q41811040 | ||
Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers | Q41882302 | ||
In situ measurements of calpain activity in isolated muscle fibres from normal and dystrophin-lacking mdx mice | Q42512800 | ||
Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions | Q43258728 | ||
The cytoprotective role of taurine in exercise-induced muscle injury | Q44055712 | ||
Enhanced dystrophic progression in mdx mice by exercise and beneficial effects of taurine and insulin-like growth factor-1. | Q44255035 | ||
The alteration of calcium homeostasis in adult dystrophic mdx muscle fibers is worsened by a chronic exercise in vivo | Q45098242 | ||
Multiple pathological events in exercised dystrophic mdx mice are targeted by pentoxifylline: outcome of a large array of in vivo and ex vivo tests. | Q45129880 | ||
A combined metabolomic and proteomic investigation of the effects of a failure to express dystrophin in the mouse heart | Q46043712 | ||
Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy | Q46113965 | ||
Gentamicin treatment in exercised mdx mice: Identification of dystrophin-sensitive pathways and evaluation of efficacy in work-loaded dystrophic muscle | Q46434974 | ||
Taurine depletion caused by knocking out the taurine transporter gene leads to cardiomyopathy with cardiac atrophy | Q46648922 | ||
P433 | issue | 3 | |
P921 | main subject | mdx mouse | Q24976962 |
P304 | page(s) | 243-256 | |
P577 | publication date | 2011-04-01 | |
P1433 | published in | Neuropathology and Applied Neurobiology | Q7002494 |
P1476 | title | Evaluation of potential synergistic action of a combined treatment with alpha-methyl-prednisolone and taurine on the mdx mouse model of Duchenne muscular dystrophy | |
P478 | volume | 37 |
Q57821110 | A long-term treatment with taurine prevents cardiac dysfunction in mdx mice |
Q43845526 | Beneficial effects of high dose taurine treatment in juvenile dystrophic mdx mice are offset by growth restriction. |
Q47349229 | Benefits of Prenatal Taurine Supplementation in Preventing the Onset of Acute Damage in the Mdx Mouse. |
Q45871995 | ECM-Related Myopathies and Muscular Dystrophies: Pros and Cons of Protein Therapies |
Q46463712 | Effects of prednisolone on the dystrophin-associated proteins in the blood-brain barrier and skeletal muscle of dystrophic mdx mice |
Q38603674 | Enalapril treatment discloses an early role of angiotensin II in inflammation- and oxidative stress-related muscle damage in dystrophic mdx mice |
Q36146630 | Increased taurine in pre-weaned juvenile mdx mice greatly reduces the acute onset of myofibre necrosis and dystropathology and prevents inflammation. |
Q40219200 | Increasing taurine intake and taurine synthesis improves skeletal muscle function in the mdx mouse model for Duchenne muscular dystrophy. |
Q37246026 | Levels of inflammation and oxidative stress, and a role for taurine in dystropathology of the Golden Retriever Muscular Dystrophy dog model for Duchenne Muscular Dystrophy |
Q26772002 | Metabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular Dystrophy |
Q24568176 | Molecular and cell-based therapies for muscle degenerations: a road under construction |
Q36925191 | Novel compounds for the treatment of Duchenne muscular dystrophy: emerging therapeutic agents |
Q26849430 | Pre-clinical drug tests in the mdx mouse as a model of dystrophinopathies: an overview |
Q96113189 | Safety issues and harmful pharmacological interactions of nutritional supplements in Duchenne muscular dystrophy: considerations for Standard of Care and emerging virus outbreaks |
Q57064365 | Taurine and Methylprednisolone Administration at Close Proximity to the Onset of Muscle Degeneration Is Ineffective at Attenuating Force Loss in the Hind-Limb of 28 Days Mice |
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Q34077151 | The different impact of a high fat diet on dystrophic mdx and control C57Bl/10 mice |
Q51625827 | The effect of taurine and β-alanine supplementation on taurine transporter protein and fatigue resistance in skeletal muscle from mdx mice. |
Q38351283 | What has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease? |
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