BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 9272155)

  • 1. 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]  

  • 2. Characterization of a KCNQ1/KVLQT1 polymorphism in Asian families with LQT2: implications for genetic testing.
    Sharma D; Glatter KA; Timofeyev V; Tuteja D; Zhang Z; Rodriguez J; Tester DJ; Low R; Scheinman MM; Ackerman MJ; Chiamvimonvat N
    J Mol Cell Cardiol; 2004 Jul; 37(1):79-89. PubMed ID: 15242738
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
    Li H; Chen Q; Moss AJ; Robinson J; Goytia V; Perry JC; Vincent GM; Priori SG; Lehmann MH; Denfield SW; Duff D; Kaine S; Shimizu W; Schwartz PJ; Wang Q; Towbin JA
    Circulation; 1998 Apr; 97(13):1264-9. PubMed ID: 9570196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.
    Donger C; Denjoy I; Berthet M; Neyroud N; Cruaud C; Bennaceur M; Chivoret G; Schwartz K; Coumel P; Guicheney P
    Circulation; 1997 Nov; 96(9):2778-81. PubMed ID: 9386136
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
    Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
    J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family.
    Ackerman MJ; Schroeder JJ; Berry R; Schaid DJ; Porter CJ; Michels VV; Thibodeau SN
    Pediatr Res; 1998 Aug; 44(2):148-53. PubMed ID: 9702906
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. The long QT syndromes: genetic basis and clinical implications.
    Chiang CE; Roden DM
    J Am Coll Cardiol; 2000 Jul; 36(1):1-12. PubMed ID: 10898405
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.
    Neyroud N; Denjoy I; Donger C; Gary F; Villain E; Leenhardt A; Benali K; Schwartz K; Coumel P; Guicheney P
    Eur J Hum Genet; 1998; 6(2):129-33. PubMed ID: 9781056
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. [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]  

  • 16. Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred.
    Saarinen K; Swan H; Kainulainen K; Toivonen L; Viitasalo M; Kontula K
    Hum Mutat; 1998; 11(2):158-65. PubMed ID: 9482580
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.
    Neyroud N; Richard P; Vignier N; Donger C; Denjoy I; Demay L; Shkolnikova M; Pesce R; Chevalier P; Hainque B; Coumel P; Schwartz K; Guicheney P
    Circ Res; 1999 Feb; 84(3):290-7. PubMed ID: 10024302
    [TBL] [Abstract][Full Text] [Related]  

  • 20. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
    Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
    Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.