BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

422 related articles for article (PubMed ID: 15950200)

  • 1. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
    Thomas D; Wimmer AB; Karle CA; Licka M; Alter M; Khalil M; Ulmer HE; Kathöfer S; Kiehn J; Katus HA; Schoels W; Koenen M; Zehelein J
    Cardiovasc Res; 2005 Aug; 67(3):487-97. PubMed ID: 15950200
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1.
    Thomas D; Khalil M; Alter M; Schweizer PA; Karle CA; Wimmer AB; Licka M; Katus HA; Koenen M; Ulmer HE; Zehelein J
    J Mol Cell Cardiol; 2010 Jan; 48(1):230-7. PubMed ID: 19540844
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1.
    Heijman J; Spätjens RL; Seyen SR; Lentink V; Kuijpers HJ; Boulet IR; de Windt LJ; David M; Volders PG
    Circ Res; 2012 Jan; 110(2):211-9. PubMed ID: 22095730
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness.
    Oertli A; Rinné S; Moss R; Kääb S; Seemann G; Beckmann BM; Decher N
    Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33498651
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome.
    Zehelein J; Thomas D; Khalil M; Wimmer AB; Koenen M; Licka M; Wu K; Kiehn J; Brockmeier K; Kreye VA; Karle CA; Katus HA; Ulmer HE; Schoels W
    Biochim Biophys Acta; 2004 Nov; 1690(3):185-92. PubMed ID: 15511625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes.
    Li W; Du R; Wang QF; Tian L; Yang JG; Song ZF
    Biochem Biophys Res Commun; 2009 May; 383(2):206-9. PubMed ID: 19348785
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
    Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
    J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.
    Yamashita F; Horie M; Kubota T; Yoshida H; Yumoto Y; Kobori A; Ninomiya T; Kono Y; Haruna T; Tsuji K; Washizuka T; Takano M; Otani H; Sasayama S; Aizawa Y
    J Mol Cell Cardiol; 2001 Feb; 33(2):197-207. PubMed ID: 11162126
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1.
    Aidery P; Kisselbach J; Schweizer PA; Becker R; Katus HA; Thomas D
    Gene; 2012 Dec; 511(1):26-33. PubMed ID: 23000022
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.
    Wang Z; Li H; Moss AJ; Robinson J; Zareba W; Knilans T; Bowles NE; Towbin JA
    Mol Genet Metab; 2002 Apr; 75(4):308-16. PubMed ID: 12051962
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.
    Wei J; Fish FA; Myerburg RJ; Roden DM; George AL
    Hum Mutat; 2000 Apr; 15(4):387-8. PubMed ID: 10737999
    [TBL] [Abstract][Full Text] [Related]  

  • 15. LQTS in Northern BC: homozygosity for KCNQ1 V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function.
    Jackson HA; McIntosh S; Whittome B; Asuri S; Casey B; Kerr C; Tang A; Arbour LT
    Clin Genet; 2014 Jul; 86(1):85-90. PubMed ID: 23844633
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.
    Zhang S; Yin K; Ren X; Wang P; Zhang S; Cheng L; Yang J; Liu JY; Liu M; Wang QK
    BMC Med Genet; 2008 Apr; 9():24. PubMed ID: 18400097
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abnormal KCNQ1 trafficking influences disease pathogenesis in hereditary long QT syndromes (LQT1).
    Wilson AJ; Quinn KV; Graves FM; Bitner-Glindzicz M; Tinker A
    Cardiovasc Res; 2005 Aug; 67(3):476-86. PubMed ID: 15935335
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.
    Bhuiyan ZA; Momenah TS; Amin AS; Al-Khadra AS; Alders M; Wilde AA; Mannens MM
    Prog Biophys Mol Biol; 2008; 98(2-3):319-27. PubMed ID: 19027783
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
    Neyroud N; Tesson F; Denjoy I; Leibovici M; Donger C; Barhanin J; Fauré S; Gary F; Coumel P; Petit C; Schwartz K; Guicheney P
    Nat Genet; 1997 Feb; 15(2):186-9. PubMed ID: 9020846
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.
    Casimiro MC; Knollmann BC; Yamoah EN; Nie L; Vary JC; Sirenko SG; Greene AE; Grinberg A; Huang SP; Ebert SN; Pfeifer K
    Genomics; 2004 Sep; 84(3):555-64. PubMed ID: 15498462
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.