BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 9445165)

  • 1. Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome.
    Duggal P; Vesely MR; Wattanasirichaigoon D; Villafane J; Kaushik V; Beggs AH
    Circulation; 1998 Jan; 97(2):142-6. PubMed ID: 9445165
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular genetics in the hereditary form of long QT syndrome].
    Georgijević Milić L
    Med Pregl; 2000; 53(1-2):51-4. PubMed ID: 10953551
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular genetics of the long QT syndrome: clinical aspects].
    Sepp R; Csanády M
    Orv Hetil; 1999 Nov; 140(47):2633-8. PubMed ID: 10613047
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
    Splawski I; Shen J; Timothy KW; Lehmann MH; Priori S; Robinson JL; Moss AJ; Schwartz PJ; Towbin JA; Vincent GM; Keating MT
    Circulation; 2000 Sep; 102(10):1178-85. PubMed ID: 10973849
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.
    Chen Q; Zhang D; Gingell RL; Moss AJ; Napolitano C; Priori SG; Schwartz PJ; Kehoe E; Robinson JL; Schulze-Bahr E; Wang Q; Towbin JA
    Circulation; 1999 Mar; 99(10):1344-7. PubMed ID: 10077519
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The long QT syndrome: ion channel diseases of the heart.
    Ackerman MJ
    Mayo Clin Proc; 1998 Mar; 73(3):250-69. PubMed ID: 9511785
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene.
    van den Berg MH; Wilde AA; Robles de Medina EO; Meyer H; Geelen JL; Jongbloed RJ; Wellens HJ; Geraedts JP
    Hum Genet; 1997 Sep; 100(3-4):356-61. PubMed ID: 9272155
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.
    Chouabe C; Neyroud N; Guicheney P; Lazdunski M; Romey G; Barhanin J
    EMBO J; 1997 Sep; 16(17):5472-9. PubMed ID: 9312006
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A recessive variant of the Romano-Ward long-QT syndrome?
    Priori SG; Schwartz PJ; Napolitano C; Bianchi L; Dennis A; De Fusco M; Brown AM; Casari G
    Circulation; 1998 Jun; 97(24):2420-5. PubMed ID: 9641694
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.
    Schmitt N; Schwarz M; Peretz A; Abitbol I; Attali B; Pongs O
    EMBO J; 2000 Feb; 19(3):332-40. PubMed ID: 10654932
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.
    Wollnik B; Schroeder BC; Kubisch C; Esperer HD; Wieacker P; Jentsch TJ
    Hum Mol Genet; 1997 Oct; 6(11):1943-9. PubMed ID: 9302275
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Molecular biology of the long QT syndrome: impact on management.
    Priori SG; Napolitano C; Paganini V; Cantù F; Schwartz PJ
    Pacing Clin Electrophysiol; 1997 Aug; 20(8 Pt 2):2052-7. PubMed ID: 9272507
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome.
    Faridi R; Tona R; Brofferio A; Hoa M; Olszewski R; Schrauwen I; Assir MZK; Bandesha AA; Khan AA; Rehman AU; Brewer C; Ahmed W; Leal SM; Riazuddin S; Boyden SE; Friedman TB
    Hum Mutat; 2019 Feb; 40(2):162-176. PubMed ID: 30461122
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations.
    Wattanasirichaigoon D; Vesely MR; Duggal P; Levine JC; Blume ED; Wolff GS; Edwards SB; Beggs AH
    Am J Med Genet; 1999 Oct; 86(5):470-6. PubMed ID: 10508990
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [KCNQ 1 (KvLQT1) missense mutation causing congenital long QT syndrome (Jervell-Lange-Nielsen) in a Mexican family].
    Márquez MF; Ramos-Kuri M; Hernández-Pacheco G; Estrada J; Fabregat JR; Pérez-Vielma N; Gómez-Flores J; González-Hermosillo A; Cárdenas M; Vargas-Alarcón G
    Arch Cardiol Mex; 2006; 76(3):257-62. PubMed ID: 17091796
    [TBL] [Abstract][Full Text] [Related]  

  • 18. KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1.
    Vyas B; Puri RD; Namboodiri N; Nair M; Sharma D; Movva S; Saxena R; Bohora S; Aggarwal N; Vora A; Kumar J; Singh T; Verma IC
    Am J Med Genet A; 2016 Jun; 170(6):1510-9. PubMed ID: 27041150
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.
    Mohammad-Panah R; Demolombe S; Neyroud N; Guicheney P; Kyndt F; van den Hoff M; Baró I; Escande D
    Am J Hum Genet; 1999 Apr; 64(4):1015-23. PubMed ID: 10090886
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
    Jongbloed RJ; Wilde AA; Geelen JL; Doevendans P; Schaap C; Van Langen I; van Tintelen JP; Cobben JM; Beaufort-Krol GC; Geraedts JP; Smeets HJ
    Hum Mutat; 1999; 13(4):301-10. PubMed ID: 10220144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.