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 *

118 related articles for article (PubMed ID: 17560885)

  • 1. A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndrome.
    Pellegrino PL; Bafunno V; Ieva R; Brunetti ND; Mavilio G; Sessa F; Grimaldi M; Margaglione M; Di Biase M
    Am J Cardiol; 2007 Jun; 99(12):1737-40. PubMed ID: 17560885
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death.
    Zhang Y; Zhou N; Jiang W; Peng J; Wan H; Huang C; Xie Z; Huang CL; Grace AA; Ma A
    Eur J Pediatr; 2007 Sep; 166(9):927-33. PubMed ID: 17171344
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].
    Du R; Ren FX; Yang JG; Yuan GH; Zhang SY; Kang CL; Li W; Gui L; Li J
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Jun; 27(3):289-94. PubMed ID: 16038262
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.
    Hedley PL; Kanters JK; Dembic M; Jespersen T; Skibsbye L; Aidt FH; Eschen O; Graff C; Behr ER; Schlamowitz S; Corfield V; McKenna WJ; Christiansen M
    Circ Cardiovasc Genet; 2013 Oct; 6(5):452-61. PubMed ID: 24021552
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.
    Krahn AD; Wang J; Spindler B; Skanes AC; Yee R; Klein GJ; Hegele RA
    Am Heart J; 2000 Jul; 140(1):146-9. PubMed ID: 10874277
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family.
    Zamorano-León JJ; Alonso-Orgaz S; Moreno J; Cinza R; García-Torrent MJ; Pérez-Castellano N; Pérez-Villacastín J; Macaya C; López-Farré AJ
    Int J Cardiol; 2010 Jul; 142(2):206-8. PubMed ID: 19136169
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Romano-Ward long QT syndrome: identification of a HERG mutation in a Taiwanese kindred.
    Lee-Chen GJ; Tai DY; Chu CH; Teng YN
    J Formos Med Assoc; 1999 Sep; 98(9):649-52. PubMed ID: 10560244
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The long QT syndrome from the bedside to molecular genetic laboratory. The history of the first described Hungarian family].
    Csanády M; Sepp R
    Orv Hetil; 2005 Sep; 146(39):2011-6. PubMed ID: 16265869
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular diagnostics of families with long-QT syndrome.
    Moric-Janiszewska E; Głowacka M
    Cardiol J; 2012; 19(2):159-67. PubMed ID: 22461049
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel nonsense mutation Y652X in the S6/pore region of human ether-go-go gene found in a long QT syndrome family.
    Sun Y; Zhang P; Li X; Zhang H; Li J; Liu G; Guo J
    Scand Cardiovasc J; 2009 Jun; 43(3):181-6. PubMed ID: 19034806
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG.
    Hayashi K; Shimizu M; Ino H; Yamaguchi M; Terai H; Hoshi N; Higashida H; Terashima N; Uno Y; Kanaya H; Mabuchi H
    Clin Sci (Lond); 2004 Aug; 107(2):175-82. PubMed ID: 15043509
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A novel mutation of the KCNH2 gene in a family with congenital long QT syndrome].
    Lian J; Zhou J; Huang X; Wang Y; Yang X; Li D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb; 27(1):77-80. PubMed ID: 20140874
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
    Johnson WH; Yang P; Yang T; Lau YR; Mostella BA; Wolff DJ; Roden DM; Benson DW
    Pediatr Res; 2003 May; 53(5):744-8. PubMed ID: 12621127
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.
    Satler CA; Walsh EP; Vesely MR; Plummer MH; Ginsburg GS; Jacob HJ
    Am J Med Genet; 1996 Oct; 65(1):27-35. PubMed ID: 8914737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [DNA-based diagnostics of long QT syndrome].
    Berge KE; Haugaa KH; Anfinsen OG; Früh A; Hallerud M; Jonsrud C; Øyen N; Gjesdal K; Amlie JP; Leren TP
    Tidsskr Nor Laegeforen; 2005 Oct; 125(20):2783-6. PubMed ID: 16244680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
    Crotti L; Lundquist AL; Insolia R; Pedrazzini M; Ferrandi C; De Ferrari GM; Vicentini A; Yang P; Roden DM; George AL; Schwartz PJ
    Circulation; 2005 Aug; 112(9):1251-8. PubMed ID: 16116052
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome.
    Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Kaneda T; Mabuchi H; Sumita R; Oshima T; Hoshi N; Higashida H
    Clin Sci (Lond); 2005 Feb; 108(2):143-50. PubMed ID: 15500450
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.
    Hong K; Bjerregaard P; Gussak I; Brugada R
    J Cardiovasc Electrophysiol; 2005 Apr; 16(4):394-6. PubMed ID: 15828882
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.