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 *

267 related articles for article (PubMed ID: 20400777)

  • 21. 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]  

  • 22. Single nucleotide polymorphism map of five long-QT genes.
    Aydin A; Bähring S; Dahm S; Guenther UP; Uhlmann R; Busjahn A; Luft FC
    J Mol Med (Berl); 2005 Feb; 83(2):159-65. PubMed ID: 15599693
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS; Yang YW; Lin YN; Lin KH; Chang KC; Chang JG
    Int Heart J; 2015; 56(4):450-3. PubMed ID: 26118593
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
    Tester DJ; Medeiros-Domingo A; Will ML; Haglund CM; Ackerman MJ
    Mayo Clin Proc; 2012 Jun; 87(6):524-39. PubMed ID: 22677073
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
    Christiansen M; Hedley PL; Theilade J; Stoevring B; Leren TP; Eschen O; Sørensen KM; Tybjærg-Hansen A; Ousager LB; Pedersen LN; Frikke-Schmidt R; Aidt FH; Hansen MG; Hansen J; Bloch Thomsen PE; Toft E; Henriksen FL; Bundgaard H; Jensen HK; Kanters JK
    BMC Med Genet; 2014 Mar; 15():31. PubMed ID: 24606995
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.
    Tzimas I; Zingraf JC; Bajanowski T; Poetsch M
    Int J Legal Med; 2016 Nov; 130(6):1575-1579. PubMed ID: 27460199
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
    Paulussen AD; Gilissen RA; Armstrong M; Doevendans PA; Verhasselt P; Smeets HJ; Schulze-Bahr E; Haverkamp W; Breithardt G; Cohen N; Aerssens J
    J Mol Med (Berl); 2004 Mar; 82(3):182-8. PubMed ID: 14760488
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
    Kapa S; Tester DJ; Salisbury BA; Harris-Kerr C; Pungliya MS; Alders M; Wilde AA; Ackerman MJ
    Circulation; 2009 Nov; 120(18):1752-60. PubMed ID: 19841300
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?
    Kiehne N; Kauferstein S
    Forensic Sci Int Genet; 2007 Jun; 1(2):170-4. PubMed ID: 19083750
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Explaining sudden infant death with cardiac arrhythmias: Complete exon sequencing of nine cardiac arrhythmia genes in Dutch SIDS cases highlights new and known DNA variants.
    Liebrechts-Akkerman G; Liu F; van Marion R; Dinjens WNM; Kayser M
    Forensic Sci Int Genet; 2020 May; 46():102266. PubMed ID: 32145446
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases.
    Tu E; Bagnall RD; Duflou J; Semsarian C
    Brain Pathol; 2011 Mar; 21(2):201-8. PubMed ID: 20875080
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 25th anniversary of the International Long-QT Syndrome Registry: an ongoing quest to uncover the secrets of long-QT syndrome.
    Moss AJ; Schwartz PJ
    Circulation; 2005 Mar; 111(9):1199-201. PubMed ID: 15753228
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
    Wang F; Liu Y; Liao H; Xue Y; Zhan X; Fang X; Liang Y; Wei W; Rao F; Zhang Q; Deng H; Lin Y; Liu F; Lin W; Zhang B; Wu S
    Cardiology; 2020; 145(1):38-45. PubMed ID: 31751991
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
    Pfeufer A; Sanna S; Arking DE; Müller M; Gateva V; Fuchsberger C; Ehret GB; Orrú M; Pattaro C; Köttgen A; Perz S; Usala G; Barbalic M; Li M; Pütz B; Scuteri A; Prineas RJ; Sinner MF; Gieger C; Najjar SS; Kao WH; Mühleisen TW; Dei M; Happle C; Möhlenkamp S; Crisponi L; Erbel R; Jöckel KH; Naitza S; Steinbeck G; Marroni F; Hicks AA; Lakatta E; Müller-Myhsok B; Pramstaller PP; Wichmann HE; Schlessinger D; Boerwinkle E; Meitinger T; Uda M; Coresh J; Kääb S; Abecasis GR; Chakravarti A
    Nat Genet; 2009 Apr; 41(4):407-14. PubMed ID: 19305409
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance.
    Mints Y; Zipunnikov V; Khurram I; Calkins H; Nazarian S
    Ann Noninvasive Electrocardiol; 2014 Jan; 19(1):63-9. PubMed ID: 24460807
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. The association between SCN5A, KCNQ1 and KCNE1 gene polymorphisms and complex ventricular arrhythmias in survivors of myocardial infarction.
    Olszak-Waśkiewicz M; Kubik L; Dziuk M; Sidło E; Kucharczyk K; Kaczanowski R
    Kardiol Pol; 2008 Aug; 66(8):845-53; discussion 854-5. PubMed ID: 18803136
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.
    Napolitano C; Priori SG; Schwartz PJ; Bloise R; Ronchetti E; Nastoli J; Bottelli G; Cerrone M; Leonardi S
    JAMA; 2005 Dec; 294(23):2975-80. PubMed ID: 16414944
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.
    Jimmy JJ; Chen CY; Yeh HM; Chiu WY; Yu CC; Liu YB; Tsai CT; Lo LW; Yeh SF; Lai LP
    Chin Med J (Engl); 2014; 127(8):1482-6. PubMed ID: 24762593
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.