These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 26346102)

  • 1. Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2.
    Wu ZJ; Huang Y; Fu YC; Zhao XJ; Zhu C; Zhang Y; Xu B; Zhu QL; Li Y
    J Geriatr Cardiol; 2015 Jul; 12(4):394-401. PubMed ID: 26346102
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Action potential clamp and mefloquine sensitivity of recombinant 'I KS' channels incorporating the V307L KCNQ1 mutation.
    El Harchi A; McPate MJ; Zhang YH; Zhang H; Hancox JC
    J Physiol Pharmacol; 2010 Apr; 61(2):123-31. PubMed ID: 20436212
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.
    Hasegawa K; Ohno S; Ashihara T; Itoh H; Ding WG; Toyoda F; Makiyama T; Aoki H; Nakamura Y; Delisle BP; Matsuura H; Horie M
    Heart Rhythm; 2014 Jan; 11(1):67-75. PubMed ID: 24096004
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
    Deschênes D; Acharfi S; Pouliot V; Hegele R; Krahn A; Daleau P; Chahine M
    Can J Physiol Pharmacol; 2003 Feb; 81(2):129-34. PubMed ID: 12710526
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differential effects of the β-adrenoceptor blockers carvedilol and metoprolol on SQT1- and SQT2-mutant channels.
    Bodi I; Franke G; Pantulu ND; Wu K; Perez-Feliz S; Bode C; Zehender M; zur Hausen A; Brunner M; Odening KE
    J Cardiovasc Electrophysiol; 2013 Oct; 24(10):1163-71. PubMed ID: 23718892
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome.
    Aizawa Y; Ueda K; Scornik F; Cordeiro JM; Wu Y; Desai M; Guerchicoff A; Nagata Y; Iesaka Y; Kimura A; Hiraoka M; Antzelevitch C
    J Cardiovasc Electrophysiol; 2007 Sep; 18(9):972-7. PubMed ID: 17655673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome.
    Hu D; Li Y; Zhang J; Pfeiffer R; Gollob MH; Healey J; Harrell DT; Makita N; Abe H; Sun Y; Guo J; Zhang L; Yan G; Mah D; Walsh EP; Leopold HB; Giustetto C; Gaita F; Zienciuk-Krajka A; Mazzanti A; Priori SG; Antzelevitch C; Barajas-Martinez H
    JACC Clin Electrophysiol; 2017 Jul; 3(7):727-743. PubMed ID: 29759541
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome.
    Moreno C; Oliveras A; de la Cruz A; Bartolucci C; Muñoz C; Salar E; Gimeno JR; Severi S; Comes N; Felipe A; González T; Lambiase P; Valenzuela C
    Cardiovasc Res; 2015 Sep; 107(4):613-23. PubMed ID: 26168993
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in the KCNH2 gene associated with short QT syndrome.
    Sun Y; Quan XQ; Fromme S; Cox RH; Zhang P; Zhang L; Guo D; Guo J; Patel C; Kowey PR; Yan GX
    J Mol Cell Cardiol; 2011 Mar; 50(3):433-41. PubMed ID: 21130771
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pro-arrhythmogenic Effects of the V141M KCNQ1 Mutation in Short QT Syndrome and Its Potential Therapeutic Targets: Insights from Modeling.
    Lee HC; Rudy Y; Liang H; Chen CC; Luo CH; Sheu SH; Cui J
    J Med Biol Eng; 2017 Oct; 37(5):780-789. PubMed ID: 29213224
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
    Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Mabuchi H; Hoshi N; Higashida H
    Clin Sci (Lond); 2003 Apr; 104(4):377-82. PubMed ID: 12653681
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A novel KCNQ1 mutation in Chinese with congenital long QT syndrome].
    Liang L; Du ZD; Cai LL; Wu JX; Zheng T; Qi TX
    Zhonghua Er Ke Za Zhi; 2003 Oct; 41(10):724-7. PubMed ID: 14731347
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents.
    Hattori T; Makiyama T; Akao M; Ehara E; Ohno S; Iguchi M; Nishio Y; Sasaki K; Itoh H; Yokode M; Kita T; Horie M; Kimura T
    Cardiovasc Res; 2012 Mar; 93(4):666-73. PubMed ID: 22155372
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long QT 1 mutation KCNQ1A344V increases local anesthetic sensitivity of the slowly activating delayed rectifier potassium current.
    Siebrands CC; Binder S; Eckhoff U; Schmitt N; Friederich P
    Anesthesiology; 2006 Sep; 105(3):511-20. PubMed ID: 16931984
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional effects of a KCNQ1 mutation associated with the long QT syndrome.
    Boulet IR; Raes AL; Ottschytsch N; Snyders DJ
    Cardiovasc Res; 2006 Jun; 70(3):466-74. PubMed ID: 16564513
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domain.
    Kimoto K; Kinoshita K; Yokoyama T; Hata Y; Komatsu T; Tsushima E; Nishide K; Yamaguchi Y; Mizumaki K; Tabata T; Inoue H; Nishida N; Fukurotani K
    Biochem Biophys Res Commun; 2013 Oct; 440(2):283-8. PubMed ID: 24070608
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of a novel Long QT syndrome mutation G52R-KCNE1 in a Chinese family.
    Ma L; Lin C; Teng S; Chai Y; Bähring R; Vardanyan V; Li L; Pongs O; Hui R
    Cardiovasc Res; 2003 Sep; 59(3):612-9. PubMed ID: 14499862
    [TBL] [Abstract][Full Text] [Related]  

  • 18. LQT1 mutations in KCNQ1 C-terminus assembly domain suppress IKs using different mechanisms.
    Aromolaran AS; Subramanyam P; Chang DD; Kobertz WR; Colecraft HM
    Cardiovasc Res; 2014 Dec; 104(3):501-11. PubMed ID: 25344363
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.
    Biliczki P; Girmatsion Z; Brandes RP; Harenkamp S; Pitard B; Charpentier F; Hébert TE; Hohnloser SH; Baró I; Nattel S; Ehrlich JR
    Heart Rhythm; 2009 Dec; 6(12):1792-801. PubMed ID: 19959132
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The
    Wang Y; Eldstrom J; Fedida D
    Mol Pharmacol; 2020 Feb; 97(2):132-144. PubMed ID: 31722973
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.