Search Results - "Musaraj, Kejla"
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Effects of Nandrolone in the Counteraction of Skeletal Muscle Atrophy in a Mouse Model of Muscle Disuse: Molecular Biology and Functional Evaluation
Published in PloS one (11-06-2015)“…Muscle disuse produces severe atrophy and a slow-to-fast phenotype transition in the postural Soleus (Sol) muscle of rodents. Antioxidants, amino-acids and…”
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Risk of Myopathy in Patients in Therapy with Statins: Identification of Biological Markers in a Pilot Study
Published in Frontiers in pharmacology (27-07-2017)“…Statin therapy may induce skeletal muscle damage ranging from myalgia to severe rhabdomyolysis. Our previous preclinical studies showed that statin treatment…”
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Statin-induced myotoxicity is exacerbated by aging: A biophysical and molecular biology study in rats treated with atorvastatin
Published in Toxicology and applied pharmacology (01-09-2016)“…Statin-induced skeletal muscle damage in rats is associated to the reduction of the resting sarcolemmal chloride conductance (gCl) and ClC-1 chloride channel…”
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Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies
Published in The FASEB journal (01-10-2016)“…Myotonia congenita is an inherited disease that is characterized by impaired muscle relaxation after contraction caused by loss-of-function mutations in the…”
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Protein kinase C theta (PKCθ) modulates the ClC-1 chloride channel activity and skeletal muscle phenotype: a biophysical and gene expression study in mouse models lacking the PKCθ
Published in Pflügers Archiv (01-12-2014)“…In skeletal muscle, the resting chloride conductance (gCl), due to the ClC-1 chloride channel, controls the sarcolemma electrical stability. Indeed,…”
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Cisplatin-Induced Cachexia in rats Causes Alterations in Skeletal Muscle Calcium Homeostasis
Published in Biophysical journal (27-01-2015)Get full text
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Multidisciplinary study of a new CIC‐1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies
Published in The FASEB journal (01-10-2016)“…ABSTRACT Myotonia congenita is an inherited disease that is characterized by impaired muscle relaxation after contraction caused by loss‐of‐function mutations…”
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Protein kinase C theta (PKC[theta]) modulates the ClC-1 chloride channel activity and skeletal muscle phenotype: a biophysical and gene expression study in mouse models lacking the PKC[theta]
Published in Pflügers Archiv (01-12-2014)“…In skeletal muscle, the resting chloride conductance (gCl), due to the ClC-1 chloride channel, controls the sarcolemma electrical stability. Indeed,…”
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