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S C Cannon

Showing results (31-40 of 46) with videos related to

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Biophysical Journal|March 1, 1997
Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysisL J Hayward, R H Brown, S C Cannon
The Journal of Physiology|July 14, 1998
Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293ID S Green, A L George, S C Cannon
Neurology|May 5, 1999
Defective slow inactivation of sodium channels contributes to familial periodic paralysisL J Hayward, G M Sandoval, S C Cannon
American Journal of Otolaryngology|July 1, 1990
Effect of electrical stimulation on middle latency response in the guinea pigS C Cannon, J M Miller, J Crowther, et al.
Journal of Neurophysiology|May 1, 1995
Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysisS C Cannon, L J Hayward, J Beech, et al.
Annals of Neurology|August 1, 1997
A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphismD S Green, L J Hayward, A L George, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 11, 2000
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivationA F Struyk, K A Scoggan, D E Bulman, et al.
Brain Research. Molecular Brain Research|December 1, 1996
Sequence of the voltage-gated sodium channel beta1-subunit in wild-type and in quivering miceC L Grosson, S C Cannon, D P Corey, et al.
Human Molecular Genetics|June 1, 1993
The cloning and expression of a sodium channel beta 1-subunit cDNA from human brainA I McClatchey, S C Cannon, S A Slaugenhaupt, et al.
Acta Oto-Laryngologica|July 1, 1985
The effect of the rotational magnification of corrective spectacles on the quantitative evaluation of the VORS C Cannon, R J Leigh, D S Zee, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Biophysical Journal|March 1, 1997
Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysisL J Hayward, R H Brown, S C Cannon
The Journal of Physiology|July 14, 1998
Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293ID S Green, A L George, S C Cannon
Neurology|May 5, 1999
Defective slow inactivation of sodium channels contributes to familial periodic paralysisL J Hayward, G M Sandoval, S C Cannon
American Journal of Otolaryngology|July 1, 1990
Effect of electrical stimulation on middle latency response in the guinea pigS C Cannon, J M Miller, J Crowther, et al.
Journal of Neurophysiology|May 1, 1995
Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysisS C Cannon, L J Hayward, J Beech, et al.
Annals of Neurology|August 1, 1997
A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphismD S Green, L J Hayward, A L George, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 11, 2000
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivationA F Struyk, K A Scoggan, D E Bulman, et al.
Brain Research. Molecular Brain Research|December 1, 1996
Sequence of the voltage-gated sodium channel beta1-subunit in wild-type and in quivering miceC L Grosson, S C Cannon, D P Corey, et al.
Human Molecular Genetics|June 1, 1993
The cloning and expression of a sodium channel beta 1-subunit cDNA from human brainA I McClatchey, S C Cannon, S A Slaugenhaupt, et al.
Acta Oto-Laryngologica|July 1, 1985
The effect of the rotational magnification of corrective spectacles on the quantitative evaluation of the VORS C Cannon, R J Leigh, D S Zee, et al.
Pageof 5