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 *

308 related articles for article (PubMed ID: 15192825)

  • 1. [The mutation scanning of KCNQ1 gene for 31 long QT syndrome families].
    Li P; Li CL; Hu DY; Liu WL; Qin XG; Li YT; Li ZM; Li L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun; 21(3):236-9. PubMed ID: 15192825
    [TBL] [Abstract][Full Text] [Related]  

  • 2. KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome.
    Herbert E; Trusz-Gluza M; Moric E; Smiłowska-Dzielicka E; Mazurek U; Wilczok T
    Med Sci Monit; 2002 Oct; 8(10):RA240-8. PubMed ID: 12388934
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
    Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Mabuchi H; Hoshi N; Higashida H
    Clin Sci (Lond); 2003 Apr; 104(4):377-82. PubMed ID: 12653681
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
    Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
    J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.
    Shimizu W; Horie M; Ohno S; Takenaka K; Yamaguchi M; Shimizu M; Washizuka T; Aizawa Y; Nakamura K; Ohe T; Aiba T; Miyamoto Y; Yoshimasa Y; Towbin JA; Priori SG; Kamakura S
    J Am Coll Cardiol; 2004 Jul; 44(1):117-25. PubMed ID: 15234419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
    Jongbloed R; Marcelis C; Velter C; Doevendans P; Geraedts J; Smeets H
    Hum Mutat; 2002 Nov; 20(5):382-91. PubMed ID: 12402336
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
    Lupoglazoff JM; Denjoy I; Villain E; Fressart V; Simon F; Bozio A; Berthet M; Benammar N; Hainque B; Guicheney P
    J Am Coll Cardiol; 2004 Mar; 43(5):826-30. PubMed ID: 14998624
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.
    Kobori A; Sarai N; Shimizu W; Nakamura Y; Murakami Y; Makiyama T; Ohno S; Takenaka K; Ninomiya T; Fujiwara Y; Matsuoka S; Takano M; Noma A; Kita T; Horie M
    J Cardiovasc Electrophysiol; 2004 Feb; 15(2):190-9. PubMed ID: 15028050
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
    Ohno S; Toyoda F; Zankov DP; Yoshida H; Makiyama T; Tsuji K; Honda T; Obayashi K; Ueyama H; Shimizu W; Miyamoto Y; Kamakura S; Matsuura H; Kita T; Horie M
    Hum Mutat; 2009 Apr; 30(4):557-63. PubMed ID: 19306396
    [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. Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.
    Yamashita F; Horie M; Kubota T; Yoshida H; Yumoto Y; Kobori A; Ninomiya T; Kono Y; Haruna T; Tsuji K; Washizuka T; Takano M; Otani H; Sasayama S; Aizawa Y
    J Mol Cell Cardiol; 2001 Feb; 33(2):197-207. PubMed ID: 11162126
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype.
    Lande G; Kyndt F; Baró I; Chabannes D; Boisseau P; Pony JC; Escande D; Le Marec H
    Eur Heart J; 2001 Mar; 22(5):410-22. PubMed ID: 11207083
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1.
    Thomas D; Khalil M; Alter M; Schweizer PA; Karle CA; Wimmer AB; Licka M; Katus HA; Koenen M; Ulmer HE; Zehelein J
    J Mol Cell Cardiol; 2010 Jan; 48(1):230-7. PubMed ID: 19540844
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
    Deschênes D; Acharfi S; Pouliot V; Hegele R; Krahn A; Daleau P; Chahine M
    Can J Physiol Pharmacol; 2003 Feb; 81(2):129-34. PubMed ID: 12710526
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.
    Gouas L; Bellocq C; Berthet M; Potet F; Demolombe S; Forhan A; Lescasse R; Simon F; Balkau B; Denjoy I; Hainque B; Baró I; Guicheney P;
    Cardiovasc Res; 2004 Jul; 63(1):60-8. PubMed ID: 15194462
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.