BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1056 related articles for article (PubMed ID: 12442276)

  • 21. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
    Zareba W; Moss AJ; Locati EH; Lehmann MH; Peterson DR; Hall WJ; Schwartz PJ; Vincent GM; Priori SG; Benhorin J; Towbin JA; Robinson JL; Andrews ML; Napolitano C; Timothy K; Zhang L; Medina A;
    J Am Coll Cardiol; 2003 Jul; 42(1):103-9. PubMed ID: 12849668
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.
    Grunnet M; Behr ER; Calloe K; Hofman-Bang J; Till J; Christiansen M; McKenna WJ; Olesen SP; Schmitt N
    Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.
    Van Langen IM; Birnie E; Alders M; Jongbloed RJ; Le Marec H; Wilde AA
    J Med Genet; 2003 Feb; 40(2):141-5. PubMed ID: 12566525
    [No Abstract]   [Full Text] [Related]  

  • 24. Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis.
    Larsen LA; Johnson M; Brown C; Christiansen M; Frank-Hansen R; Vuust J; Andersen PS
    Hum Mutat; 2001 Nov; 18(5):451-7. PubMed ID: 11668638
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
    Tester DJ; Cronk LB; Carr JL; Schulz V; Salisbury BA; Judson RS; Ackerman MJ
    Heart Rhythm; 2006 Jul; 3(7):815-21. PubMed ID: 16818214
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.
    Larsen LA; Andersen PS; Kanters J; Svendsen IH; Jacobsen JR; Vuust J; Wettrell G; Tranebjaerg L; Bathen J; Christiansen M
    Clin Chem; 2001 Aug; 47(8):1390-5. PubMed ID: 11468227
    [TBL] [Abstract][Full Text] [Related]  

  • 27. KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel.
    Tinel N; Diochot S; Borsotto M; Lazdunski M; Barhanin J
    EMBO J; 2000 Dec; 19(23):6326-30. PubMed ID: 11101505
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.
    Jimmy JJ; Chen CY; Yeh HM; Chiu WY; Yu CC; Liu YB; Tsai CT; Lo LW; Yeh SF; Lai LP
    Chin Med J (Engl); 2014; 127(8):1482-6. PubMed ID: 24762593
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C; Zhao Q; Su T; Tang S; Lv G; Liu H; Quan L; Cheng J
    Forensic Sci Int; 2013 Sep; 231(1-3):82-7. PubMed ID: 23890619
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.
    Liu L; Hayashi K; Kaneda T; Ino H; Fujino N; Uchiyama K; Konno T; Tsuda T; Kawashiri MA; Ueda K; Higashikata T; Shuai W; Kupershmidt S; Higashida H; Yamagishi M
    Heart Rhythm; 2013 Jan; 10(1):61-7. PubMed ID: 23010577
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous.
    Schulze-Bahr E; Haverkamp W; Wedekind H; Rubie C; Hördt M; Borggrefe M; Assmann G; Breithardt G; Funke H
    Hum Genet; 1997 Oct; 100(5-6):573-6. PubMed ID: 9341873
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identical twins with long QT syndrome associated with a missense mutation in the S4 region of the HERG.
    Hayashi K; Shimizu M; Ino H; Okeie K; Yamaguchi M; Yasuda T; Fujino N; Fujii H; Fujita S; Mabuchi H
    Jpn Heart J; 2000 May; 41(3):399-404. PubMed ID: 10987356
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.
    Paulussen A; Matthijs G; Gewillig M; Verhasselt P; Cohen N; Aerssens J
    Genet Test; 2003; 7(1):57-61. PubMed ID: 12820704
    [TBL] [Abstract][Full Text] [Related]  

  • 34. KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
    Chen S; Zhang L; Bryant RM; Vincent GM; Flippin M; Lee JC; Brown E; Zimmerman F; Rozich R; Szafranski P; Oberti C; Sterba R; Marangi D; Tchou PJ; Chung MK; Wang Q
    Clin Genet; 2003 Apr; 63(4):273-82. PubMed ID: 12702160
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.
    Lupoglazoff JM; Denjoy I; Berthet M; Neyroud N; Demay L; Richard P; Hainque B; Vaksmann G; Klug D; Leenhardt A; Maillard G; Coumel P; Guicheney P
    Circulation; 2001 Feb; 103(8):1095-101. PubMed ID: 11222472
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
    Christiansen M; Hedley PL; Theilade J; Stoevring B; Leren TP; Eschen O; Sørensen KM; Tybjærg-Hansen A; Ousager LB; Pedersen LN; Frikke-Schmidt R; Aidt FH; Hansen MG; Hansen J; Bloch Thomsen PE; Toft E; Henriksen FL; Bundgaard H; Jensen HK; Kanters JK
    BMC Med Genet; 2014 Mar; 15():31. PubMed ID: 24606995
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
    Lupoglazoff JM; Denjoy I; Villain E; Fressart V; Simon F; Bozio A; Berthet M; Benammar N; Hainque B; Guicheney P
    J Am Coll Cardiol; 2004 Mar; 43(5):826-30. PubMed ID: 14998624
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
    Inoue M; Shimizu M; Ino H; Yamaguchi M; Terai H; Hayashi K; Kiyama M; Sakata K; Hayashi T; Mabuchi H
    Circ J; 2003 Jun; 67(6):495-8. PubMed ID: 12808265
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates.
    Chevalier P; Rodriguez C; Bontemps L; Miquel M; Kirkorian G; Rousson R; Potet F; Schott JJ; Baró I; Touboul P
    Cardiovasc Res; 2001 May; 50(2):386-98. PubMed ID: 11334843
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].
    Zhao QH; Liu C; Lu LW; Lü GL; Liu H; Tang SB; Quan L; Cheng JD
    Fa Yi Xue Za Zhi; 2012 Oct; 28(5):337-41, 346. PubMed ID: 23213782
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 53.