BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 24561538)

  • 1. KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmia.
    Kalscheur MM; Vaidyanathan R; Orland KM; Abozeid S; Fabry N; Maginot KR; January CT; Makielski JC; Eckhardt LL
    Heart Rhythm; 2014 May; 11(5):885-94. PubMed ID: 24561538
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia.
    Vega AL; Tester DJ; Ackerman MJ; Makielski JC
    Circ Arrhythm Electrophysiol; 2009 Oct; 2(5):540-7. PubMed ID: 19843922
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic Loss of
    Reilly L; Alvarado FJ; Lang D; Abozeid S; Van Ert H; Spellman C; Warden J; Makielski JC; Glukhov AV; Eckhardt LL
    Circ Arrhythm Electrophysiol; 2020 Sep; 13(9):e008638. PubMed ID: 32931337
    [TBL] [Abstract][Full Text] [Related]  

  • 4. KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.
    Eckhardt LL; Farley AL; Rodriguez E; Ruwaldt K; Hammill D; Tester DJ; Ackerman MJ; Makielski JC
    Heart Rhythm; 2007 Mar; 4(3):323-9. PubMed ID: 17341397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicry.
    Barajas-Martinez H; Hu D; Ontiveros G; Caceres G; Desai M; Burashnikov E; Scaglione J; Antzelevitch C
    Circ Cardiovasc Genet; 2011 Feb; 4(1):51-7. PubMed ID: 21148745
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents.
    Hattori T; Makiyama T; Akao M; Ehara E; Ohno S; Iguchi M; Nishio Y; Sasaki K; Itoh H; Yokode M; Kita T; Horie M; Kimura T
    Cardiovasc Res; 2012 Mar; 93(4):666-73. PubMed ID: 22155372
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inward Rectifier Potassium Channels (Kir2.x) and Caveolin-3 Domain-Specific Interaction: Implications for Purkinje Cell-Dependent Ventricular Arrhythmias.
    Vaidyanathan R; Van Ert H; Haq KT; Morotti S; Esch S; McCune EC; Grandi E; Eckhardt LL
    Circ Arrhythm Electrophysiol; 2018 Jan; 11(1):e005800. PubMed ID: 29326130
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.
    Ördög B; Hategan L; Kovács M; Seprényi G; Kohajda Z; Nagy I; Hegedűs Z; Környei L; Jost N; Katona M; Szekeres M; Forster T; Papp JG; Varró A; Sepp R
    Can J Physiol Pharmacol; 2015 Jul; 93(7):569-75. PubMed ID: 26103554
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.
    Haruna Y; Kobori A; Makiyama T; Yoshida H; Akao M; Doi T; Tsuji K; Ono S; Nishio Y; Shimizu W; Inoue T; Murakami T; Tsuboi N; Yamanouchi H; Ushinohama H; Nakamura Y; Yoshinaga M; Horigome H; Aizawa Y; Kita T; Horie M
    Hum Mutat; 2007 Feb; 28(2):208. PubMed ID: 17221872
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotype variability in patients carrying KCNJ2 mutations.
    Kimura H; Zhou J; Kawamura M; Itoh H; Mizusawa Y; Ding WG; Wu J; Ohno S; Makiyama T; Miyamoto A; Naiki N; Wang Q; Xie Y; Suzuki T; Tateno S; Nakamura Y; Zang WJ; Ito M; Matsuura H; Horie M
    Circ Cardiovasc Genet; 2012 Jun; 5(3):344-53. PubMed ID: 22589293
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome.
    Hosaka Y; Hanawa H; Washizuka T; Chinushi M; Yamashita F; Yoshida T; Komura S; Watanabe H; Aizawa Y
    J Mol Cell Cardiol; 2003 Apr; 35(4):409-15. PubMed ID: 12689820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity.
    Tani Y; Miura D; Kurokawa J; Nakamura K; Ouchida M; Shimizu K; Ohe T; Furukawa T
    J Mol Cell Cardiol; 2007 Aug; 43(2):187-96. PubMed ID: 17582433
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PA-6 inhibits inward rectifier currents carried by V93I and D172N gain-of-function K
    Ji Y; Veldhuis MG; Zandvoort J; Romunde FL; Houtman MJC; Duran K; van Haaften G; Zangerl-Plessl EM; Takanari H; Stary-Weinzinger A; van der Heyden MAG
    J Biomed Sci; 2017 Jul; 24(1):44. PubMed ID: 28711067
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome.
    Lu CW; Lin JH; Rajawat YS; Jerng H; Rami TG; Sanchez X; DeFreitas G; Carabello B; DeMayo F; Kearney DL; Miller G; Li H; Pfaffinger PJ; Bowles NE; Khoury DS; Towbin JA
    J Med Genet; 2006 Aug; 43(8):653-9. PubMed ID: 16571646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The interaction of caveolin 3 protein with the potassium inward rectifier channel Kir2.1: physiology and pathology related to long qt syndrome 9 (LQT9).
    Vaidyanathan R; Vega AL; Song C; Zhou Q; Tan BH; Berger S; Makielski JC; Eckhardt LL
    J Biol Chem; 2013 Jun; 288(24):17472-80. PubMed ID: 23640888
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3.
    Moreno-Manuel AI; Macías Á; Cruz FM; Gutiérrez LK; Martínez F; González-Guerra A; Martínez Carrascoso I; Bermúdez-Jimenez FJ; Sánchez-Pérez P; Vera-Pedrosa ML; Ruiz-Robles JM; Bernal JA; Jalife J
    Cardiovasc Res; 2024 Apr; 120(5):490-505. PubMed ID: 38261726
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cardiac potassium inward rectifier Kir2: Review of structure, regulation, pharmacology, and arrhythmogenesis.
    Reilly L; Eckhardt LL
    Heart Rhythm; 2021 Aug; 18(8):1423-1434. PubMed ID: 33857643
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Andersen mutations of KCNJ2 suppress the native inward rectifier current IK1 in a dominant-negative fashion.
    Lange PS; Er F; Gassanov N; Hoppe UC
    Cardiovasc Res; 2003 Aug; 59(2):321-7. PubMed ID: 12909315
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kir2.1 Interactome Mapping Uncovers PKP4 as a Modulator of the Kir2.1-Regulated Inward Rectifier Potassium Currents.
    Park SS; Ponce-Balbuena D; Kuick R; Guerrero-Serna G; Yoon J; Mellacheruvu D; Conlon KP; Basrur V; Nesvizhskii AI; Jalife J; Rual JF
    Mol Cell Proteomics; 2020 Sep; 19(9):1436-1449. PubMed ID: 32541000
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphic ventricular tachycardia and KCNJ2 mutations.
    Chun TU; Epstein MR; Dick M; Andelfinger G; Ballester L; Vanoye CG; George AL; Benson DW
    Heart Rhythm; 2004 Jul; 1(2):235-41. PubMed ID: 15851159
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.