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The Journal of Physiology|December 17, 2002
Expression of a calpastatin transgene slows muscle wasting and obviates changes in myosin isoform expression during murine muscle disuseJames G Tidball, Melissa J SpencerHuman Molecular Genetics|October 2, 2002
Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathologyMelissa J Spencer, Ronald L MellgrenThe Journal of Clinical Investigation|April 17, 2012
Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2HElena Kudryashova, Irina Kramerova, Melissa J SpencerThe Journal of Biological Chemistry|November 13, 2014
Autolytic activation of calpain 3 proteinase is facilitated by calmodulin proteinNatalia Ermolova, Irina Kramerova, Melissa J SpencerHandbook of Clinical Neurology|April 19, 2011
Limb-girdle muscular dystrophy 2H and the role of TRIM32Perry B Shieh, Elena Kudryashova, Melissa J SpencerBiochimica Et Biophysica Acta. Molecular Cell Research|December 25, 2016
Outside in: The matrix as a modifier of muscular dystrophyMattia Quattrocelli, Melissa J Spencer, Elizabeth M McNallyBiochimica Et Biophysica Acta|August 29, 2006
Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)Irina Kramerova, Jacques S Beckmann, Melissa J SpencerJournal of Molecular Biology|October 26, 2005
Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actinElena Kudryashova, Dmitri Kudryashov, Irina Kramerova, et al.Human Molecular Genetics|June 18, 2005
Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathwayIrina Kramerova, Elena Kudryashova, Gayathri Venkatraman, et al.Molecular and Cellular Biology|September 20, 2006
Regulation of the M-cadherin-beta-catenin complex by calpain 3 during terminal stages of myogenic differentiationIrina Kramerova, Elena Kudryashova, Benjamin Wu, et al.Pageof 7