Stephen C. Cannon

Affiliations: 
2015- Physiology David Geffen School of Medicine at UCLA, Los Angeles, CA, United States 
Area:
channelopathies, skeletal muscle, sodium channels
Website:
https://cannonlab.dgsom.ucla.edu/pages/
Google:
"Stephen Cannon"
Mean distance: 13.82 (cluster 6)
 
SNBCP
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Quiñonez M, DiFranco M, Wu F, et al. (2023) Retigabine suppresses loss of force in mouse models of hypokalaemic periodic paralysis. Brain : a Journal of Neurology
DiFranco M, Cannon S. (2022) Voltage-Dependent Ca Release Is Impaired in Hypokalemic Periodic Paralysis Caused by Ca1.1-R528H but not by Na1.4-R669H. American Journal of Physiology. Cell Physiology
Savalli N, Angelini M, Steccanella F, et al. (2021) The distinct role of the four voltage sensors of the skeletal CaV1.1 channel in voltage-dependent activation. The Journal of General Physiology. 153
Wu F, Quinonez M, Cannon SC. (2021) Gating pore currents occur in CaV1.1 domain III mutants associated with HypoPP. The Journal of General Physiology. 153
Cannon SC. (2021) Epilepsy channelopathies go neddy: stabilizing NaV1.1 channels by neddylation. The Journal of Clinical Investigation. 131
Kubota T, Wu F, Vicart S, et al. (2020) Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor. Brain Communications. 2: fcaa103
Cannon SC. (2020) A role for external Ca2+ in maintaining muscle contractility in periodic paralysis. The Journal of General Physiology. 152
Stunnenberg B, LoRusso S, Arnold WD, et al. (2020) Guidelines on clinical presentation and management of non-dystrophic myotonias. Muscle & Nerve
Elia N, Nault T, McMillan HJ, et al. (2020) Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in . Frontiers in Neurology. 11: 181
Elia N, Nault T, McMillan HJ, et al. (2020) Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L769V Mutation in . Frontiers in Neurology. 11: 77
See more...