Article Commentary: Commentary on the Present State of Knowledge for Myoblast Transfer Therapy ‌ Miranda D. Grounds

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Myoblast Transfer Therapy in the New Millennium ‌ Miranda D. Grounds

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Cromolyn administration (to block mast cell degranulation) reduces necrosis of dystrophic muscle in mdx mice ‌ Hannah G. Radley, Miranda D. Grounds

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Exposure to Tissue Culture Conditions Can Adversely Affect Myoblast Behavior in Vivo in Whole Muscle Grafts: Implications for Myoblast Transfer Therapy ‌ Gayle M. Smythe, Miranda D. Grounds

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Why Do Cultured Transplanted Myoblasts Die in Vivo? DNA Quantification Shows Enhanced Survival of Donor Male Myoblasts in Host Mice Depleted of CD4 and CD8 Cells or NK1.1 Cells ‌ Stuart I. Hodgetts, Manfred W. Beilharz, Anthony A. Scalzo, Miranda D. Grounds

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Striking denervation of neuromuscular junctions without lumbar motoneuron loss in geriatric mouse muscle. ‌ Ruth Jinfen Chai, Jana Vukovic, Sarah Dunlop, Miranda D Grounds, Thea Shavlakadze

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A Blood Biomarker for Duchenne Muscular Dystrophy Shows That Oxidation State of Albumin Correlates with Protein Oxidation and Damage in Mdx Muscle ‌ Basma A. Al-Mshhdani, Miranda D. Grounds, Peter G. Arthur, Jessica R. Terrill

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Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy ‌ Miranda D. Grounds, Hannah G. Radley, Gordon S. Lynch, Kanneboyina Nagaraju, Annamaria De Luca

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Dysferlin-deficiency has greater impact on function of slow muscles, compared with fast, in aged BLAJ mice. ‌ Erin M Lloyd, Hongyang Xu, Robyn M Murphy, Miranda D Grounds, Gavin J Pinniger

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Correction: Dysferlin-deficiency has greater impact on function of slow muscles, compared with fast, in aged BLAJ mice. ‌ Erin M Lloyd, Hongyang Xu, Robyn M Murphy, Miranda D Grounds, Gavin J Pinniger

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Beneficial effects of high dose taurine treatment in juvenile dystrophic mdx mice are offset by growth restriction. ‌ Jessica R Terrill, Gavin J Pinniger, Keshav V Nair, Miranda D Grounds, Peter G Arthur

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Oxidised Albumin Levels in Plasma and Skeletal Muscle as Biomarkers of Disease Progression and Treatment Efficacy in Dystrophic <i>mdx</i> Mice ‌ Jessica R. Terrill, Angelo Patrick R. Bautista, Irene Tsioutsias, Miranda D. Grounds, Peter G. Arthur

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MicroRNA and Long Non-coding RNA Regulation in Skeletal Muscle From Growth to Old Age Shows Striking Dysregulation of the Callipyge Locus ‌ Jasmine Mikovic, Kate Sadler, Lauren Butchart, Sarah Voisin, Frederico Gerlinger-Romero, Paul Della Gatta, Miranda D. Grounds, Séverine Lamon

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Dystropathology increases energy expenditure and protein turnover in the mdx mouse model of duchenne muscular dystrophy. ‌ Hannah G Radley-Crabb, Juan C Marini, Horacio A Sosa, Liliana I Castillo, Miranda D Grounds, Marta L Fiorotto

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Dysferlin deficiency alters lipid metabolism and remodels the skeletal muscle lipidome in mice ‌ Vanessa R. Haynes, Stacey N. Keenan, Jackie Bayliss, Erin M. Lloyd, Peter J. Meikle, Miranda D. Grounds, Matthew J. Watt

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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 ‌ Jessica R. Terrill, Marisa N. Duong, Rufus Turner, Caroline Le Guiner, Amber Boyatzis, Anthony J. Kettle, Miranda D. Grounds, Peter G. Arthur

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A Comparison between Real-Time Quantitative PCR and DNA Hybridization for Quantitation of Male DNA following Myoblast Transplantation ‌ Erika Bosio, Tracey F. Lee-Pullen, Clayton T. Fragall, Manfred W. Beilharz, Alayne L. Bennett, Miranda D. Grounds, Stuart I. Hodgetts, Leanne M. Sammels

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Macrophage Depletion in Elderly Mice Improves Response to Tumor Immunotherapy, Increases Anti-tumor T Cell Activity and Reduces Treatment-Induced Cachexia ‌ Lelinh Duong, Hannah G. Radley-Crabb, Joanne K. Gardner, Federica Tomay, Danielle E. Dye, Miranda D. Grounds, Fiona J. Pixley, Delia J. Nelson, Connie Jackaman

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Ageing contributes to phenotype transition in a mouse model of periodic paralysis ‌ Karen J. Suetterlin, S. Veronica Tan, Roope Mannikko, Rahul Phadke, Michael Orford, Simon Eaton, Avan A. Sayer, Miranda D. Grounds, Emma Matthews, Linda Greensmith, Michael G. Hanna

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Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the <i>mdx</i> Mouse Model for Duchenne Muscular Dystrophy ‌ Jessica R. Terrill, Corinne Huchet, Caroline Le Guiner, Aude Lafoux, Dorian Caudal, Ankita Tulangekar, Robert J. Bryson-Richardson, Tamar E. Sztal, Miranda D. Grounds, Peter G. Arthur

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