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  • Link to full list of publications by S C Cannon
  • Elia, N, Palmio, J., Sampedro Castaneda, M., Shieh, P.B., Quinonez, M., Souminen, T., Hanna, M., Mannikko, R., Udd, B., Cannon, S.C. (2019) Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4.  Neurology 92:e1405-e1415.
  • Mi, W., Wu, F., Quinonez, M., DiFranco, M., Cannon, S.C. (2019)  Recovery from acidosis is a robust trigger for loss of force in murine hypokalemic periodic paralysis.  J. Gen. Physiol. 151:555-566.
  • Lin, M.A., Cannon, S.C., Papazian, D.M. (2018)  Kv4.2 autism and epilepsy mutation enhances inactivation of closed channels but impairs access to inactivated state after opening. PNAS 115:E3550-E3568. 
  • Wu, F., Quinonez, M., DiFranco, M., Cannon, S.C. (2018). Stac3 enhances expression of human CaV1.1 in Xenopus oocytes and reveals gating pore currents in HypoPP mutant channels. J Gen Physiol. 150:475-489
  • Cannon S.C. (2017) An atypical mutation of CaV1.1 supports a common mechanism for susceptibility to hypokalemic periodic paralysis.  J. Gen. Physiol. 149:1061-1064.
  • Wu, F.F, Mi, W., Struyk A.S., Cannon, S.C. (2016) Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.  Brain 39:1688-1699
  • Nelson, B.R., Makarewich, C.A., Anderson, D.M., Winders, B.R., Troupes, C.D., Wu, F.F., Reese, A.L., McAnally, J.R., Chen X., Kavalali, E.T., Cannon, S.C., Houser, S.R., Bassel-Duby, R., Olson, E.N. (2016) A peptide endoced by a transcript annotated as long noncoding RNA enhances SERCA activity in muscle. Science 351:271-275.
  • Cannon, S.C. (2015). Channelopathies of Skeletal Muscle Excitability. Compr Physiol 5: 761-790. doi: 10.1002/cphy.c140062
  • Wu, F.F., Mi W., Cannon, S.C. (2013)  Beneficial effects of bumetanide in a CaV1.1-R528H mouse model of hypokalemic periodic paralysis.  Brain 136:3766-3774
  • Nelson, B.R., Wu, F.F., Liu, Y., Anderson, D.M., McAnally, J., Lin, W., Cannon, S.C., Bassel-Duby, R., Olson, E.N. (2013) The skeletal muscle-specific T-tubule protein STAC3 mediates voltage-induced Ca2+ release and contractility.  Proc. Nat. Acad. Sci.  110:11881-886.
  • Wu, F.F, Mi, W., Hernandex-Ochoa, E.O., Burns, D.K., Fu, Y., Gray, H.F., Struyk, A.F., Schneider, M.F., Cannon, S.C. (2012).  A calcium channel knock-in mutant (CaV1.1-R528H) mouse model of hypokalemic periodic paralysis. J. Clin Invest 122:4580-91.