223 related articles for article (PubMed ID: 9929487)
1. Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia.
Takahashi MP; Cannon SC
Biophys J; 1999 Feb; 76(2):861-8. PubMed ID: 9929487
[TBL] [Abstract][Full Text] [Related]
2. Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channel.
Takahashi MP; Cannon SC
J Physiol; 2001 Dec; 537(Pt 3):701-14. PubMed ID: 11744749
[TBL] [Abstract][Full Text] [Related]
3. Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis.
Hayward LJ; Brown RH; Cannon SC
Biophys J; 1997 Mar; 72(3):1204-19. PubMed ID: 9138567
[TBL] [Abstract][Full Text] [Related]
4. A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivation.
Wu FF; Gordon E; Hoffman EP; Cannon SC
J Physiol; 2005 Jun; 565(Pt 2):371-80. PubMed ID: 15774523
[TBL] [Abstract][Full Text] [Related]
5. Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I.
Green DS; George AL; Cannon SC
J Physiol; 1998 Aug; 510 ( Pt 3)(Pt 3):685-94. PubMed ID: 9660885
[TBL] [Abstract][Full Text] [Related]
6. The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation.
Struyk AF; Scoggan KA; Bulman DE; Cannon SC
J Neurosci; 2000 Dec; 20(23):8610-7. PubMed ID: 11102465
[TBL] [Abstract][Full Text] [Related]
7. Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenita.
Fleischhauer R; Mitrovic N; Deymeer F; Lehmann-Horn F; Lerche H
Pflugers Arch; 1998 Oct; 436(5):757-65. PubMed ID: 9716710
[TBL] [Abstract][Full Text] [Related]
8. Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.
Webb J; Cannon SC
Neurology; 2008 Mar; 70(10):755-61. PubMed ID: 17898326
[TBL] [Abstract][Full Text] [Related]
9. A novel dominant mutation of the Nav1.4 alpha-subunit domain I leading to sodium channel myotonia.
Petitprez S; Tiab L; Chen L; Kappeler L; Rösler KM; Schorderet D; Abriel H; Burgunder JM
Neurology; 2008 Nov; 71(21):1669-75. PubMed ID: 19015483
[TBL] [Abstract][Full Text] [Related]
10. Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker.
Hayward LJ; Brown RH; Cannon SC
J Gen Physiol; 1996 May; 107(5):559-76. PubMed ID: 8740371
[TBL] [Abstract][Full Text] [Related]
11. Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5.
Bendahhou S; Cummins TR; Kula RW; Fu YH; Ptácek LJ
Neurology; 2002 Apr; 58(8):1266-72. PubMed ID: 11971097
[TBL] [Abstract][Full Text] [Related]
12. A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation.
Bouhours M; Luce S; Sternberg D; Willer JC; Fontaine B; Tabti N
J Physiol; 2005 Jun; 565(Pt 2):415-27. PubMed ID: 15790667
[TBL] [Abstract][Full Text] [Related]
13. Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation.
Bendahhou S; Cummins TR; Tawil R; Waxman SG; Ptácek LJ
J Neurosci; 1999 Jun; 19(12):4762-71. PubMed ID: 10366610
[TBL] [Abstract][Full Text] [Related]
14. Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans.
Bouhours M; Sternberg D; Davoine CS; Ferrer X; Willer JC; Fontaine B; Tabti N
J Physiol; 2004 Feb; 554(Pt 3):635-47. PubMed ID: 14617673
[TBL] [Abstract][Full Text] [Related]
15. A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivation.
Wu FF; Takahashi MP; Pegoraro E; Angelini C; Colleselli P; Cannon SC; Hoffman EP
Neurology; 2001 Apr; 56(7):878-84. PubMed ID: 11294924
[TBL] [Abstract][Full Text] [Related]
16. Comparison of slow inactivation in human heart and rat skeletal muscle Na+ channel chimaeras.
O'Reilly JP; Wang SY; Kallen RG; Wang GK
J Physiol; 1999 Feb; 515 ( Pt 1)(Pt 1):61-73. PubMed ID: 9925878
[TBL] [Abstract][Full Text] [Related]
17. Spectrum of sodium channel disturbances in the nondystrophic myotonias and periodic paralyses.
Cannon SC
Kidney Int; 2000 Mar; 57(3):772-9. PubMed ID: 10720928
[TBL] [Abstract][Full Text] [Related]
18. Defective slow inactivation of sodium channels contributes to familial periodic paralysis.
Hayward LJ; Sandoval GM; Cannon SC
Neurology; 1999 Apr; 52(7):1447-53. PubMed ID: 10227633
[TBL] [Abstract][Full Text] [Related]
19. Sodium channel defects in myotonia and periodic paralysis.
Cannon SC
Annu Rev Neurosci; 1996; 19():141-64. PubMed ID: 8833439
[TBL] [Abstract][Full Text] [Related]
20. A global defect in scaling relationship between electrical activity and availability of muscle sodium channels in hyperkalemic periodic paralysis.
Melamed-Frank M; Marom S
Pflugers Arch; 1999 Jul; 438(2):213-7. PubMed ID: 10370108
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]