BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 33574382)

  • 1. Long-QT founder variant T309I-Kv7.1 with dominant negative pattern may predispose delayed afterdepolarizations under β-adrenergic stimulation.
    Synková I; Bébarová M; Andršová I; Chmelikova L; Švecová O; Hošek J; Pásek M; Vít P; Valášková I; Gaillyová R; Navrátil R; Novotný T
    Sci Rep; 2021 Feb; 11(1):3573. PubMed ID: 33574382
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics.
    Piippo K; Swan H; Pasternack M; Chapman H; Paavonen K; Viitasalo M; Toivonen L; Kontula K
    J Am Coll Cardiol; 2001 Feb; 37(2):562-8. PubMed ID: 11216980
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk.
    ter Bekke RM; Haugaa KH; van den Wijngaard A; Bos JM; Ackerman MJ; Edvardsen T; Volders PG
    Eur Heart J; 2015 Jan; 36(3):179-86. PubMed ID: 25205533
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants.
    Kashiwa A; Itoh H; Makiyama T; Wada Y; Ozawa J; Kato K; Fukuyama M; Nakajima T; Ohno S; Horie M
    Heart Rhythm; 2024 Jul; 21(7):1113-1120. PubMed ID: 38367891
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
    Wong JA; Gula LJ; Klein GJ; Yee R; Skanes AC; Krahn AD
    Circ Arrhythm Electrophysiol; 2010 Apr; 3(2):120-5. PubMed ID: 20071715
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.
    Koponen M; Havulinna AS; Marjamaa A; Tuiskula AM; Salomaa V; Laitinen-Forsblom PJ; Piippo K; Toivonen L; Kontula K; Viitasalo M; Swan H
    BMC Med Genet; 2018 Apr; 19(1):56. PubMed ID: 29622001
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotype-based clinical manifestation and treatment of Chinese long QT syndrome patients with KCNQ1 mutations - R380S and W305L.
    Zhou H; Lai W; Zhu W; Xie J; Liu X; Shen Y; Yuan P; Liu Y; Cao Q; He W; Hong K
    Cardiol Young; 2016 Apr; 26(4):754-63. PubMed ID: 26344792
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation.
    Spätjens RL; Bébarová M; Seyen SR; Lentink V; Jongbloed RJ; Arens YH; Heijman J; Volders PG
    Cardiovasc Res; 2014 Oct; 104(1):216-25. PubMed ID: 25139741
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families.
    Winbo A; Stattin EL; Nordin C; Diamant UB; Persson J; Jensen SM; Rydberg A
    BMC Cardiovasc Disord; 2014 Feb; 14():22. PubMed ID: 24552659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?
    Lahtinen AM; Marjamaa A; Swan H; Kontula K
    BMC Med Genet; 2011 Jan; 12():11. PubMed ID: 21244686
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Long QT syndrome in adults.
    Sauer AJ; Moss AJ; McNitt S; Peterson DR; Zareba W; Robinson JL; Qi M; Goldenberg I; Hobbs JB; Ackerman MJ; Benhorin J; Hall WJ; Kaufman ES; Locati EH; Napolitano C; Priori SG; Schwartz PJ; Towbin JA; Vincent GM; Zhang L
    J Am Coll Cardiol; 2007 Jan; 49(3):329-37. PubMed ID: 17239714
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.
    Kobori A; Sarai N; Shimizu W; Nakamura Y; Murakami Y; Makiyama T; Ohno S; Takenaka K; Ninomiya T; Fujiwara Y; Matsuoka S; Takano M; Noma A; Kita T; Horie M
    J Cardiovasc Electrophysiol; 2004 Feb; 15(2):190-9. PubMed ID: 15028050
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.
    Fodstad H; Bendahhou S; Rougier JS; Laitinen-Forsblom PJ; Barhanin J; Abriel H; Schild L; Kontula K; Swan H
    Ann Med; 2006; 38(4):294-304. PubMed ID: 16754261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.
    Koponen M; Marjamaa A; Hiippala A; Happonen JM; Havulinna AS; Salomaa V; Lahtinen AM; Hintsa T; Viitasalo M; Toivonen L; Kontula K; Swan H
    Circ Arrhythm Electrophysiol; 2015 Aug; 8(4):815-23. PubMed ID: 26063740
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation.
    Horr S; Goldenberg I; Moss AJ; O-Uchi J; Barsheshet A; Connelly H; Gray DA; Zareba W; Lopes CM
    J Cardiovasc Electrophysiol; 2011 Feb; 22(2):193-200. PubMed ID: 20662986
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.
    Al-Hassnan ZN; Al-Fayyadh M; Al-Ghamdi B; Shafquat A; Mallawi Y; Al-Hadeq F; Tulbah S; Shinwari ZMA; Almesned A; Alakhfash A; Al Fadly F; Hersi AS; Alhayani A; Al-Hashem A; Arafah D; Dzimiri N; Meyer B; Rababh M; Al-Manea W
    Heart Rhythm; 2017 Aug; 14(8):1191-1199. PubMed ID: 28438721
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.
    Diamant UB; Vahedi F; Winbo A; Rydberg A; Stattin EL; Jensen SM; Bergfeldt L
    J Appl Physiol (1985); 2013 Nov; 115(10):1423-32. PubMed ID: 24052033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac Mechanical Alterations and Genotype Specific Differences in Subjects With Long QT Syndrome.
    Leren IS; Hasselberg NE; Saberniak J; Håland TF; Kongsgård E; Smiseth OA; Edvardsen T; Haugaa KH
    JACC Cardiovasc Imaging; 2015 May; 8(5):501-510. PubMed ID: 25890583
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.