These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 8872472)

  • 1. KVLQT1 mutations in three families with familial or sporadic long QT syndrome.
    Russell MW; Dick M; Collins FS; Brody LC
    Hum Mol Genet; 1996 Sep; 5(9):1319-24. PubMed ID: 8872472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome.
    Larsen LA; Andersen PS; Kanters JK; Jacobsen JR; Vuust J; Christiansen M
    Clin Chim Acta; 1999 Feb; 280(1-2):113-25. PubMed ID: 10090529
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome.
    Itoh T; Tanaka T; Nagai R; Kikuchi K; Ogawa S; Okada S; Yamagata S; Yano K; Yazaki Y; Nakamura Y
    Hum Genet; 1998 Sep; 103(3):290-4. PubMed ID: 9799083
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias.
    Napolitano C; Schwartz PJ; Brown AM; Ronchetti E; Bianchi L; Pinnavaia A; Acquaro G; Priori SG
    J Cardiovasc Electrophysiol; 2000 Jun; 11(6):691-6. PubMed ID: 10868744
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
    Wang Q; Curran ME; Splawski I; Burn TC; Millholland JM; VanRaay TJ; Shen J; Timothy KW; Vincent GM; de Jager T; Schwartz PJ; Toubin JA; Moss AJ; Atkinson DL; Landes GM; Connors TD; Keating MT
    Nat Genet; 1996 Jan; 12(1):17-23. PubMed ID: 8528244
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.
    Kanters JK; Larsen LA; Orholm M; Agner E; Andersen PS; Vuust J; Christiansen M
    J Cardiovasc Electrophysiol; 1998 Jun; 9(6):620-4. PubMed ID: 9654228
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. [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]  

  • 18. 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]  

  • 19. The KVLQT1 gene is not a common target for mutations in patients with various heart pathologies.
    Moric E; Herbert E; Mazurek U; Samelska J; Cholewa K; Trusz-Gluza M; Wilczok T
    J Appl Genet; 2002; 43(2):245-54. PubMed ID: 12080180
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.