BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 9302275)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk.
    Chouabe C; Neyroud N; Richard P; Denjoy I; Hainque B; Romey G; Drici MD; Guicheney P; Barhanin J
    Cardiovasc Res; 2000 Mar; 45(4):971-80. PubMed ID: 10728423
    [TBL] [Abstract][Full Text] [Related]  

  • 9. George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.
    Splawski I; Timothy KW; Vincent GM; Atkinson DL; Keating MT
    Proc Assoc Am Physicians; 1997 Sep; 109(5):504-11. PubMed ID: 9285950
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Long QT syndrome: ionic basis and arrhythmia mechanism in long QT syndrome type 1.
    Sanguinetti MC
    J Cardiovasc Electrophysiol; 2000 Jun; 11(6):710-2. PubMed ID: 10868746
    [TBL] [Abstract][Full Text] [Related]  

  • 11. IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
    Tyson J; Tranebjaerg L; Bellman S; Wren C; Taylor JF; Bathen J; Aslaksen B; Sørland SJ; Lund O; Malcolm S; Pembrey M; Bhattacharya S; Bitner-Glindzicz M
    Hum Mol Genet; 1997 Nov; 6(12):2179-85. PubMed ID: 9328483
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A dominant negative isoform of the long QT syndrome 1 gene product.
    Demolombe S; Baró I; Péréon Y; Bliek J; Mohammad-Panah R; Pollard H; Morid S; Mannens M; Wilde A; Barhanin J; Charpentier F; Escande D
    J Biol Chem; 1998 Mar; 273(12):6837-43. PubMed ID: 9506986
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
    Sanguinetti MC
    Ann N Y Acad Sci; 1999 Apr; 868():406-13. PubMed ID: 10414310
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. MinK-KvLQT1 fusion proteins, evidence for multiple stoichiometries of the assembled IsK channel.
    Wang W; Xia J; Kass RS
    J Biol Chem; 1998 Dec; 273(51):34069-74. PubMed ID: 9852064
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.
    Shalaby FY; Levesque PC; Yang WP; Little WA; Conder ML; Jenkins-West T; Blanar MA
    Circulation; 1997 Sep; 96(6):1733-6. PubMed ID: 9323054
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.