Jeffrey J. Widrick
Affiliations: | Oregon State University, Corvallis, OR |
Area:
Cell Biology, Recreation, Public HealthGoogle:
"Jeffrey Widrick"Cross-listing: PHTree
Children
Sign in to add trainee| Dena J. Garner | grad student | 2002 | Oregon State |
| Julian E. Stelzer | grad student | 2003 | Oregon State |
| Kevin Marley | grad student | 2004 | Oregon State |
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Publications
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| Samani A, Karuppasamy M, English KG, et al. (2023) DOCK3 regulates normal skeletal muscle regeneration and glucose metabolism. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 37: e23198 |
| Samani A, Karuppasamy M, English KG, et al. (2023) DOCK3 regulates normal skeletal muscle regeneration and glucose metabolism. Biorxiv : the Preprint Server For Biology |
| Hightower RM, Reid AL, Gibbs DE, et al. (2019) The SINE Compound KPT-350 Blocks Dystrophic Pathologies in DMD Zebrafish and Mice. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Lim JY, Choi SJ, Widrick JJ, et al. (2019) Passive force and viscoelastic properties of single fibers in human aging muscles. European Journal of Applied Physiology |
| Pearsall RS, Davies MV, Cannell M, et al. (2019) Follistatin-based ligand trap ACE-083 induces localized hypertrophy of skeletal muscle with functional improvement in models of neuromuscular disease. Scientific Reports. 9: 11392 |
| Regué L, Ji F, Flicker D, et al. (2019) IMP2 increases mouse skeletal muscle mass and voluntary activity by enhancing autocrine IGF2 production and optimizing muscle metabolism. Molecular and Cellular Biology |
| Serafini PR, Feyder MJ, Hightower RM, et al. (2018) A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies. Jci Insight. 3 |
| Bennett AH, O'Donohue MF, Gundry SR, et al. (2018) RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes. Plos Genetics. 14: e1007226 |
| Huntoon V, Widrick JJ, Sanchez C, et al. (2018) SPEG-deficient Skeletal Muscles Exhibit Abnormal Triad and Defective Calcium Handling. Human Molecular Genetics |
| Huntoon V, Widrick J, Sanchez C, et al. (2017) SPEG deficiency is associated with muscle weakness, triad defect, abnormal calcium handling and EC coupling Neuromuscular Disorders. 27: S230 |