Robert Grange
Affiliations: | Virginia Polytechnic Institute and State University, Blacksburg, VA, United States |
Area:
Biomedical Engineering, Recreation, Physiology BiologyGoogle:
"Robert Grange"
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Publications
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| Hamm SE, Fathalikhani DD, Bukovec KE, et al. (2021) Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice. Molecular Therapy. Methods & Clinical Development. 23: 460 |
| Hamm SE, Fathalikhani DD, Bukovec KE, et al. (2021) Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice. Molecular Therapy. Methods & Clinical Development. 21: 144-160 |
| Bukovec KE, Hu X, Borkowski M, et al. (2020) A novel ex vivo protocol to mimic human walking gait: implications for Duchenne muscular dystrophy. Journal of Applied Physiology (Bethesda, Md. : 1985) |
| Yuan C, Arora A, Garofalo AM, et al. (2020) Potential cross-talk between muscle and tendon in Duchenne muscular dystrophy. Connective Tissue Research. 1-13 |
| Barraza-Flores P, Bukovec KE, Dagda M, et al. (2020) Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of Laminin-α2 related congenital muscular dystrophy. Human Molecular Genetics |
| Dupont JB, Guo J, Renaud-Gabardos E, et al. (2019) AAV-Mediated Gene Transfer Restores a Normal Muscle Transcriptome in a Canine Model of X-Linked Myotubular Myopathy. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Capogrosso RF, Mantuano P, Cozzoli A, et al. (2017) CONTRACTILE EFFICIENCY OF DYSTROPHIC MDX MOUSE MUSCLE: IN VIVO AND EX VIVO ASSESSMENT OF ADAPTATION TO EXERCISE OF FUNCTIONAL END-POINTS. Journal of Applied Physiology (Bethesda, Md. : 1985). jap.00776.2015 |
| Sperringer JE, Grange RW. (2016) In Vitro Assays to Determine Skeletal Muscle Physiologic Function. Methods in Molecular Biology (Clifton, N.J.). 1460: 271-91 |
| Cong X, Doering J, Grange RW, et al. (2016) Defective excitation-contraction coupling is partially responsible for impaired contractility in hindlimb muscles of Stac3 knockout mice. Scientific Reports. 6: 26194 |
| Cong X, Doering J, Mazala DA, et al. (2016) The SH3 and cysteine-rich domain 3 (Stac3) gene is important to growth, fiber composition, and calcium release from the sarcoplasmic reticulum in postnatal skeletal muscle. Skeletal Muscle. 6: 17 |