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Neuromuscular Disorders : NMD|December 7, 2002
Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscleKim E Wells, Silvia Torelli, Qi Lu, et al.
Human Molecular Genetics|January 22, 2005
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophyMartin Brockington, Silvia Torelli, Paola Prandini, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 17, 2011
Restoration of the dystrophin-associated glycoprotein complex after exon skipping therapy in Duchenne muscular dystrophySebahattin Cirak, Lucy Feng, Karen Anthony, et al.
Plos One|January 5, 2011
Transgenic overexpression of LARGE induces α-dystroglycan hyperglycosylation in skeletal and cardiac muscleMartin Brockington, Silvia Torelli, Paul S Sharp, et al.
Scientific Reports|February 28, 2019
Regulation of the dystrophin-associated glycoprotein complex composition by the metabolic properties of muscle fibresSaleh Omairi, Kwan-Leong Hau, Henry Collins-Hooper, et al.
Plos One|July 30, 2013
Flow cytometry for the analysis of α-dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathiesElizabeth Stevens, Silvia Torelli, Lucy Feng, et al.
Acta Neuropathologica Communications|April 19, 2020
A high-throughput digital script for multiplexed immunofluorescent analysis and quantification of sarcolemmal and sarcomeric proteins in muscular dystrophiesDominic Scaglioni, Matthew Ellis, Francesco Catapano, et al.
Plos One|March 27, 2018
A novel high-throughput immunofluorescence analysis method for quantifying dystrophin intensity in entire transverse sections of Duchenne muscular dystrophy muscle biopsy samplesValentina Sardone, Matthew Ellis, Silvia Torelli, et al.
Molecular Therapy. Methods & Clinical Development|July 23, 2020
Myostatin Is a Quantifiable Biomarker for Monitoring Pharmaco-gene Therapy in Duchenne Muscular DystrophyVirginie Mariot, Caroline Le Guiner, Inès Barthélémy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 6, 2003
Profound skeletal muscle depletion of alpha-dystroglycan in Walker-Warburg syndromeCecilia Jiménez-Mallebrera, Silvia Torelli, Susan C Brown, et al.
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