BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

329 related articles for article (PubMed ID: 11102465)

  • 1. 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]  

  • 2. A Na+ channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore.
    Struyk AF; Cannon SC
    J Gen Physiol; 2007 Jul; 130(1):11-20. PubMed ID: 17591984
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.
    Jurkat-Rott K; Mitrovic N; Hang C; Kouzmekine A; Iaizzo P; Herzog J; Lerche H; Nicole S; Vale-Santos J; Chauveau D; Fontaine B; Lehmann-Horn F
    Proc Natl Acad Sci U S A; 2000 Aug; 97(17):9549-54. PubMed ID: 10944223
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disrupted coupling of gating charge displacement to Na+ current activation for DIIS4 mutations in hypokalemic periodic paralysis.
    Mi W; Rybalchenko V; Cannon SC
    J Gen Physiol; 2014 Aug; 144(2):137-45. PubMed ID: 25024265
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II.
    Kuzmenkin A; Muncan V; Jurkat-Rott K; Hang C; Lerche H; Lehmann-Horn F; Mitrovic N
    Brain; 2002 Apr; 125(Pt 4):835-43. PubMed ID: 11912116
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.
    Wu F; Mi W; Burns DK; Fu Y; Gray HF; Struyk AF; Cannon SC
    J Clin Invest; 2011 Oct; 121(10):4082-94. PubMed ID: 21881211
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis.
    Struyk AF; Markin VS; Francis D; Cannon SC
    J Gen Physiol; 2008 Oct; 132(4):447-64. PubMed ID: 18824591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Voltage-dependent Ca
    DiFranco M; Cannon SC
    Am J Physiol Cell Physiol; 2022 Aug; 323(2):C478-C485. PubMed ID: 35759432
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis.
    Bendahhou S; Cummins TR; Griggs RC; Fu YH; Ptácek LJ
    Ann Neurol; 2001 Sep; 50(3):417-20. PubMed ID: 11558801
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. A calcium channel mutant mouse model of hypokalemic periodic paralysis.
    Wu F; Mi W; Hernández-Ochoa EO; Burns DK; Fu Y; Gray HF; Struyk AF; Schneider MF; Cannon SC
    J Clin Invest; 2012 Dec; 122(12):4580-91. PubMed ID: 23187123
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Paramyotonia congenita mutations reveal different roles for segments S3 and S4 of domain D4 in hSkM1 sodium channel gating.
    Ji S; George AL; Horn R; Barchi RL
    J Gen Physiol; 1996 Feb; 107(2):183-94. PubMed ID: 8833340
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia.
    Francis DG; Rybalchenko V; Struyk A; Cannon SC
    Neurology; 2011 May; 76(19):1635-41. PubMed ID: 21490317
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysis.
    Carle T; Lhuillier L; Luce S; Sternberg D; Devuyst O; Fontaine B; Tabti N
    Biochem Biophys Res Commun; 2006 Sep; 348(2):653-61. PubMed ID: 16890191
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 17.