BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

391 related articles for article (PubMed ID: 10414310)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome.
    Bianchi L; Shen Z; Dennis AT; Priori SG; Napolitano C; Ronchetti E; Bryskin R; Schwartz PJ; Brown AM
    Hum Mol Genet; 1999 Aug; 8(8):1499-507. PubMed ID: 10400998
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C
    J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM
    Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Biophysical properties and molecular basis of cardiac rapid and slow delayed rectifier potassium channels.
    Mitcheson JS; Sanguinetti MC
    Cell Physiol Biochem; 1999; 9(4-5):201-16. PubMed ID: 10575198
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structural determinants and biophysical properties of HERG and KCNQ1 channel gating.
    Tristani-Firouzi M; Sanguinetti MC
    J Mol Cell Cardiol; 2003 Jan; 35(1):27-35. PubMed ID: 12623297
    [TBL] [Abstract][Full Text] [Related]  

  • 10. C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
    Berthet M; Denjoy I; Donger C; Demay L; Hammoude H; Klug D; Schulze-Bahr E; Richard P; Funke H; Schwartz K; Coumel P; Hainque B; Guicheney P
    Circulation; 1999 Mar; 99(11):1464-70. PubMed ID: 10086971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interactions of the antimalarial drug mefloquine with the human cardiac potassium channels KvLQT1/minK and HERG.
    Kang J; Chen XL; Wang L; Rampe D
    J Pharmacol Exp Ther; 2001 Oct; 299(1):290-6. PubMed ID: 11561091
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
    Splawski I; Shen J; Timothy KW; Vincent GM; Lehmann MH; Keating MT
    Genomics; 1998 Jul; 51(1):86-97. PubMed ID: 9693036
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two isoforms of the mouse ether-a-go-go-related gene coassemble to form channels with properties similar to the rapidly activating component of the cardiac delayed rectifier K+ current.
    London B; Trudeau MC; Newton KP; Beyer AK; Copeland NG; Gilbert DJ; Jenkins NA; Satler CA; Robertson GA
    Circ Res; 1997 Nov; 81(5):870-8. PubMed ID: 9351462
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cocaine blocks HERG, but not KvLQT1+minK, potassium channels.
    Zhang S; Rajamani S; Chen Y; Gong Q; Rong Y; Zhou Z; Ruoho A; January CT
    Mol Pharmacol; 2001 May; 59(5):1069-76. PubMed ID: 11306689
    [TBL] [Abstract][Full Text] [Related]  

  • 15. KvLQT1 modulates the distribution and biophysical properties of HERG. A novel alpha-subunit interaction between delayed rectifier currents.
    Ehrlich JR; Pourrier M; Weerapura M; Ethier N; Marmabachi AM; Hébert TE; Nattel S
    J Biol Chem; 2004 Jan; 279(2):1233-41. PubMed ID: 14585842
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the hminK gene cause long QT syndrome and suppress IKs function.
    Splawski I; Tristani-Firouzi M; Lehmann MH; Sanguinetti MC; Keating MT
    Nat Genet; 1997 Nov; 17(3):338-40. PubMed ID: 9354802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.
    Sanguinetti MC; Curran ME; Spector PS; Keating MT
    Proc Natl Acad Sci U S A; 1996 Mar; 93(5):2208-12. PubMed ID: 8700910
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel.
    Furutani M; Trudeau MC; Hagiwara N; Seki A; Gong Q; Zhou Z; Imamura S; Nagashima H; Kasanuki H; Takao A; Momma K; January CT; Robertson GA; Matsuoka R
    Circulation; 1999 May; 99(17):2290-4. PubMed ID: 10226095
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
    Moss AJ; Zareba W; Kaufman ES; Gartman E; Peterson DR; Benhorin J; Towbin JA; Keating MT; Priori SG; Schwartz PJ; Vincent GM; Robinson JL; Andrews ML; Feng C; Hall WJ; Medina A; Zhang L; Wang Z
    Circulation; 2002 Feb; 105(7):794-9. PubMed ID: 11854117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inhibition of cardiac delayed rectifier K+ currents by an antisense oligodeoxynucleotide against IsK (minK) and over-expression of IsK mutant D77N in neonatal mouse hearts.
    Ohyama H; Kajita H; Omori K; Takumi T; Hiramoto N; Iwasaka T; Matsuda H
    Pflugers Arch; 2001 Jun; 442(3):329-35. PubMed ID: 11484762
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.