BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 16800854)

  • 21. The evolving role of ankyrin-B in cardiovascular disease.
    Koenig SN; Mohler PJ
    Heart Rhythm; 2017 Dec; 14(12):1884-1889. PubMed ID: 28765088
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation.
    Huq AJ; Pertile MD; Davis AM; Landon H; James PA; Kline CF; Vohra J; Mohler PJ; Delatycki MB
    Heart Lung Circ; 2017 Jun; 26(6):612-618. PubMed ID: 27916589
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mechanisms and Alterations of Cardiac Ion Channels Leading to Disease: Role of Ankyrin-B in Cardiac Function.
    Sucharski HC; Dudley EK; Keith CBR; El Refaey M; Koenig SN; Mohler PJ
    Biomolecules; 2020 Jan; 10(2):. PubMed ID: 32023981
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Common human ANK2 variant confers in vivo arrhythmia phenotypes.
    Musa H; Murphy NP; Curran J; Higgins JD; Webb TR; Makara MA; Wright P; Lancione PJ; Lubbers ER; Healy JA; Smith SA; Bennett V; Hund TJ; Kline CF; Mohler PJ
    Heart Rhythm; 2016 Sep; 13(9):1932-40. PubMed ID: 27298202
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmia.
    Smith SA; Sturm AC; Curran J; Kline CF; Little SC; Bonilla IM; Long VP; Makara M; Polina I; Hughes LD; Webb TR; Wei Z; Wright P; Voigt N; Bhakta D; Spoonamore KG; Zhang C; Weiss R; Binkley PF; Janssen PM; Kilic A; Higgins RS; Sun M; Ma J; Dobrev D; Zhang M; Carnes CA; Vatta M; Rasband MN; Hund TJ; Mohler PJ
    Circulation; 2015 Feb; 131(8):695-708. PubMed ID: 25632041
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cardiac channelopathies.
    Marbán E
    Nature; 2002 Jan; 415(6868):213-8. PubMed ID: 11805845
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Susceptibility genes and modifiers for cardiac arrhythmias.
    Kääb S; Schulze-Bahr E
    Cardiovasc Res; 2005 Aug; 67(3):397-413. PubMed ID: 15949790
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The role of microRNA in cardiac excitability.
    Wang Z
    J Cardiovasc Pharmacol; 2010 Nov; 56(5):460-70. PubMed ID: 20588186
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Exon organization and novel alternative splicing of the human ANK2 gene: implications for cardiac function and human cardiac disease.
    Cunha SR; Le Scouarnec S; Schott JJ; Mohler PJ
    J Mol Cell Cardiol; 2008 Dec; 45(6):724-34. PubMed ID: 18790697
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteins.
    Ackerman MJ; Mohler PJ
    Circ Res; 2010 Aug; 107(4):457-65. PubMed ID: 20724725
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes.
    Mohler PJ; Le Scouarnec S; Denjoy I; Lowe JS; Guicheney P; Caron L; Driskell IM; Schott JJ; Norris K; Leenhardt A; Kim RB; Escande D; Roden DM
    Circulation; 2007 Jan; 115(4):432-41. PubMed ID: 17242276
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rare Variants in ANK2 Associated With Various Inherited Arrhythmia Syndromes.
    Watanabe H; Minamino T
    Circ J; 2016 Nov; 80(12):2423-2424. PubMed ID: 27818464
    [No Abstract]   [Full Text] [Related]  

  • 33. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction?
    Light PE
    J Cardiovasc Electrophysiol; 2006 May; 17 Suppl 1():S158-S161. PubMed ID: 16686673
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Defects in ankyrin-based membrane protein targeting pathways underlie atrial fibrillation.
    Cunha SR; Hund TJ; Hashemi S; Voigt N; Li N; Wright P; Koval O; Li J; Gudmundsson H; Gumina RJ; Karck M; Schott JJ; Probst V; Le Marec H; Anderson ME; Dobrev D; Wehrens XH; Mohler PJ
    Circulation; 2011 Sep; 124(11):1212-22. PubMed ID: 21859974
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dysfunction in ankyrin-based cellular pathways and human cardiac arrhythmia.
    Mohler PJ; Lowe JS; Banks S
    Future Cardiol; 2005 May; 1(3):363-71. PubMed ID: 19804119
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview.
    Smits JP; Blom MT; Wilde AA; Tan HL
    Expert Opin Pharmacother; 2008 Mar; 9(4):537-49. PubMed ID: 18312156
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why?
    Scicluna BP; Wilde AA; Bezzina CR
    J Cardiovasc Electrophysiol; 2008 Apr; 19(4):445-52. PubMed ID: 18284507
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ankyrins and Spectrins in Cardiovascular Biology and Disease.
    El Refaey MM; Mohler PJ
    Front Physiol; 2017; 8():852. PubMed ID: 29163198
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cardiac-specific overexpression of the human type 1 angiotensin II receptor causes delayed repolarization.
    Rivard K; Paradis P; Nemer M; Fiset C
    Cardiovasc Res; 2008 Apr; 78(1):53-62. PubMed ID: 18245065
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes.
    Mohler PJ; Rivolta I; Napolitano C; LeMaillet G; Lambert S; Priori SG; Bennett V
    Proc Natl Acad Sci U S A; 2004 Dec; 101(50):17533-8. PubMed ID: 15579534
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.