Stanley C. Froehner
Affiliations: | University of Washington, Seattle, Seattle, WA |
Area:
synapse formation, neuromuscular synapseGoogle:
"Stanley Froehner"Mean distance: 53433
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Publications
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| Kim MJ, Bible KL, Regnier M, et al. (2019) Simvastatin provides long-term improvement of left ventricular function and prevents cardiac fibrosis in muscular dystrophy. Physiological Reports. 7: e14018 |
| Kim MJ, Whitehead NP, Bible KL, et al. (2018) Mice lacking α-,β1- and β2-syntrophins exhibit diminished function and reduced dystrophin expression in both cardiac and skeletal muscle. Human Molecular Genetics |
| Adams ME, Odom GL, Kim MJ, et al. (2018) Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16-17. Human Molecular Genetics |
| Whitehead NP, Bible KL, Kim MJ, et al. (2016) Validation of ultrasonography for non-invasive assessment of diaphragm function in muscular dystrophy. The Journal of Physiology |
| Nanou E, Yan J, Whitehead NP, et al. (2016) Altered short-term synaptic plasticity and reduced muscle strength in mice with impaired regulation of presynaptic CaV2.1 Ca2+ channels. Proceedings of the National Academy of Sciences of the United States of America |
| Allen DG, Whitehead NP, Froehner SC. (2016) Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. Physiological Reviews. 96: 253-305 |
| Rebolledo DL, Kim MJ, Whitehead NP, et al. (2015) Sarcolemmal targeting of nNOSμ improves contractile function of mdx muscle. Human Molecular Genetics |
| Whitehead NP, Kim MJ, Bible KL, et al. (2015) A new therapeutic effect of simvastatin revealed by functional improvement in muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America |
| Eisinger K, Froehner SC, Adams ME, et al. (2015) Evaluation of the specificity of four commercially available antibodies to alpha-syntrophin. Analytical Biochemistry. 484: 99-101 |
| Hebel T, Eisinger K, Neumeier M, et al. (2015) Lipid abnormalities in alpha/beta2-syntrophin null mice are independent from ABCA1. Biochimica Et Biophysica Acta. 1851: 527-36 |