Defects in sarcolemma repair and skeletal muscle function after injury in a mouse model of Niemann-Pick type A/B disease
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M. Corrotte | R. Lovering | D. Mazala | S. Iyer | E. Chin | H. Li | N. Andrews | V. Michailowsky | B. Mittra | Y. Wang | N. W. Andrews
[1] Benjamin Sanchez,et al. Non‐invasive assessment of muscle injury in healthy and dystrophic animals with electrical impedance myography , 2017, Muscle & nerve.
[2] R. Lovering,et al. In Vivo Assessment of Muscle Contractility in Animal Studies. , 2016, Methods in molecular biology.
[3] A. Arner,et al. Immobilization of Dystrophin and Laminin α2-Chain Deficient Zebrafish Larvae In Vivo Prevents the Development of Muscular Dystrophy , 2015, PloS one.
[4] R. Grange,et al. The role of proteases in excitation-contraction coupling failure in muscular dystrophy. , 2015, American journal of physiology. Cell physiology.
[5] D. Mazala,et al. Perturbations in intracellular Ca2+ handling in skeletal muscle in the G93A*SOD1 mouse model of amyotrophic lateral sclerosis. , 2014, American journal of physiology. Cell physiology.
[6] M. Corrotte,et al. Damage control: cellular mechanisms of plasma membrane repair. , 2014, Trends in cell biology.
[7] Stephen J. P. Pratt,et al. A stepwise procedure to test contractility and susceptibility to injury for the rodent quadriceps muscle. , 2014, Journal of biological methods.
[8] J. Jaiswal,et al. Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion , 2014, Cell Death and Disease.
[9] P. Boya,et al. High sphingomyelin levels induce lysosomal damage and autophagy dysfunction in Niemann Pick disease type A , 2014, Cell Death and Differentiation.
[10] D. Mazala,et al. Perturbations in intracellular Ca handling in skeletal muscle in the G93A*SOD1 mouse model of amyotrophic lateral sclerosis , 2014 .
[11] Bryan A. Millis,et al. Caveolae internalization repairs wounded cells and muscle fibers , 2013, eLife.
[12] N. Andrews,et al. Live imaging assay for assessing the roles of Ca2+ and sphingomyelinase in the repair of pore-forming toxin wounds. , 2013, Journal of Visualized Experiments.
[13] Chang-chen Yin,et al. Shotgun proteomic analysis of sarcoplasmic reticulum preparations from rabbit skeletal muscle , 2013, Proteomics.
[14] R. Desnick,et al. Morbidity and mortality in type B Niemann–Pick disease , 2013, Genetics in Medicine.
[15] Sameer B. Shah,et al. Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles , 2013, The Journal of physiology.
[16] Sameer B. Shah,et al. An in vivo rodent model of contraction-induced injury in the quadriceps muscle. , 2012, Injury.
[17] J. Tidball,et al. Mechanisms of muscle injury, repair, and regeneration. , 2011, Comprehensive Physiology.
[18] Jianjie Ma,et al. Visualization of MG53-mediated Cell Membrane Repair Using in vivo and in vitro Systems , 2011, Journal of visualized experiments : JoVE.
[19] C. Reggiani,et al. Massive alterations of sarcoplasmic reticulum free calcium in skeletal muscle fibers lacking calsequestrin revealed by a genetically encoded probe , 2010, Proceedings of the National Academy of Sciences.
[20] C. Devlin,et al. Exocytosis of acid sphingomyelinase by wounded cells promotes endocytosis and plasma membrane repair , 2010, The Journal of cell biology.
[21] E. Schuchman. Acid sphingomyelinase, cell membranes and human disease: Lessons from Niemann–Pick disease , 2010, FEBS letters.
[22] G. Lamb. Mechanisms of excitation-contraction uncoupling relevant to activity-induced muscle fatigue. , 2009, Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme.
[23] R. Sidman,et al. Neuropathology of the acid sphingomyelinase knockout mouse model of Niemann-Pick A disease including structure–function studies associated with cerebellar Purkinje cell degeneration , 2008, Experimental Neurology.
[24] S. Brodie,et al. A Prospective, Cross-sectional Survey Study of the Natural History of Niemann-Pick Disease Type B , 2008, Pediatrics.
[25] D. Toomre,et al. Repair of injured plasma membrane by rapid Ca2+-dependent endocytosis , 2008, The Journal of cell biology.
[26] R. Lovering,et al. Recovery of function in skeletal muscle following 2 different contraction-induced injuries. , 2007, Archives of physical medicine and rehabilitation.
[27] K. Fénelon,et al. Role of calsequestrin evaluated from changes in free and total calcium concentrations in the sarcoplasmic reticulum of frog cut skeletal muscle fibres , 2007, The Journal of physiology.
[28] A. E. Rossi,et al. Sarcoplasmic reticulum: The dynamic calcium governor of muscle , 2006, Muscle & nerve.
[29] J. Lieberman,et al. Perforin triggers a plasma membrane-repair response that facilitates CTL induction of apoptosis. , 2005, Immunity.
[30] R. Lovering,et al. The contribution of contractile pre-activation to loss of function after a single lengthening contraction. , 2005, Journal of biomechanics.
[31] J. Jaffrezou,et al. UV-C Light Induces Raft-associated Acid Sphingomyelinase and JNK Activation and Translocation Independently on a Nuclear Signal* , 2005, Journal of Biological Chemistry.
[32] Anthony H. Futerman,et al. The cell biology of lysosomal storage disorders , 2004, Nature Reviews Molecular Cell Biology.
[33] K. Campbell,et al. Dysferlin and the plasma membrane repair in muscular dystrophy. , 2004, Trends in cell biology.
[34] C. Padovani,et al. Skeletal muscule fiber types in C57BL6J mice , 2004 .
[35] P. Mcneil,et al. Plasma membrane disruption: repair, prevention, adaptation. , 2003, Annual review of cell and developmental biology.
[36] Chien-Chang Chen,et al. Defective membrane repair in dysferlin-deficient muscular dystrophy , 2003, Nature.
[37] E. Gulbins. Regulation of death receptor signaling and apoptosis by ceramide. , 2003, Pharmacological research.
[38] R. Kolesnick,et al. Host defense against Pseudomonas aeruginosa requires ceramide-rich membrane rafts , 2003, Nature Medicine.
[39] R. Desnick,et al. The demographics and distribution of type B Niemann-Pick disease: novel mutations lead to new genotype/phenotype correlations. , 2002, American journal of human genetics.
[40] Hai-Shan Wu,et al. Reproductive pathology and sperm physiology in acid sphingomyelinase-deficient mice. , 2002, The American journal of pathology.
[41] G. W. Huntley,et al. Intracerebral transplantation of mesenchymal stem cells into acid sphingomyelinase-deficient mice delays the onset of neurological abnormalities and extends their life span. , 2002, The Journal of clinical investigation.
[42] P. Mcneil,et al. Repairing a torn cell surface: make way, lysosomes to the rescue. , 2002, Journal of Cell Science.
[43] O. Petersen,et al. Membrane repair: Ca2+-elicited lysosomal exocytosis , 2001, Current Biology.
[44] E. Caler,et al. Plasma Membrane Repair Is Mediated by Ca2+-Regulated Exocytosis of Lysosomes , 2001, Cell.
[45] N. Andrews,et al. Regulated secretion of conventional lysosomes. , 2000, Trends in cell biology.
[46] K. Williams,et al. Sphingomyelinase, an enzyme implicated in atherogenesis, is present in atherosclerotic lesions and binds to specific components of the subendothelial extracellular matrix. , 1999, Arteriosclerosis, thrombosis, and vascular biology.
[47] D. Allen,et al. The contribution of pH‐dependent mechanisms to fatigue at different intensities in mammalian single muscle fibres , 1998, The Journal of physiology.
[48] E. Chin,et al. The role of elevations in intracellular [Ca2+] in the development of low frequency fatigue in mouse single muscle fibres. , 1996, The Journal of physiology.
[49] D. Perl,et al. Acid sphingomyelinase deficient mice: a model of types A and B Niemann–Pick disease , 1995, Nature Genetics.
[50] P. Mcneil,et al. Disruptions of muscle fiber plasma membranes. Role in exercise-induced damage. , 1992, The American journal of pathology.
[51] J. Faulkner,et al. Contraction-induced injury: recovery of skeletal muscles in young and old mice. , 1990, The American journal of physiology.
[52] P. Mcneil,et al. Gastrointestinal cell plasma membrane wounding and resealing in vivo. , 1989, Gastroenterology.