241 related articles for article (PubMed ID: 23644778)
61. Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia.
Ai T; Fujiwara Y; Tsuji K; Otani H; Nakano S; Kubo Y; Horie M
Circulation; 2002 Jun; 105(22):2592-4. PubMed ID: 12045162
[TBL] [Abstract][Full Text] [Related]
62. Up-regulation of the inwardly rectifying K⁺ channel Kir2.1 (KCNJ2) by protein kinase B (PKB/Akt) and PIKfyve.
Munoz C; Almilaji A; Setiawan I; Föller M; Lang F
J Membr Biol; 2013 Mar; 246(3):189-97. PubMed ID: 23188060
[TBL] [Abstract][Full Text] [Related]
63. Andersen-Tawil Syndrome Is Associated With Impaired PIP
Handklo-Jamal R; Meisel E; Yakubovich D; Vysochek L; Beinart R; Glikson M; McMullen JR; Dascal N; Nof E; Oz S
Front Pharmacol; 2020; 11():672. PubMed ID: 32499698
[TBL] [Abstract][Full Text] [Related]
64. Insights in KIR2.1 channel structure and function by an evolutionary approach; cloning and functional characterization of the first reptilian inward rectifier channel KIR2.1, derived from the California kingsnake (Lampropeltis getula californiae).
Houtman MJ; Korte SM; Ji Y; Kok B; Vos MA; Stary-Weinzinger A; van der Heyden MA
Biochem Biophys Res Commun; 2014 Oct; 452(4):992-7. PubMed ID: 25223803
[TBL] [Abstract][Full Text] [Related]
65. [Andersen-Tawil syndrome: a review of its clinical and genetic diagnosis with emphasis on cardiac manifestations].
Márquez MF; Totomoch-Serra A; Vargas-Alarcón G; Cruz-Robles D; Pellizzon OA; Cárdenas M
Arch Cardiol Mex; 2014; 84(4):278-85. PubMed ID: 25270337
[TBL] [Abstract][Full Text] [Related]
66. Array comparative genomic hybridization identifies a heterozygous deletion of the entire KCNJ2 gene as a cause of sudden cardiac death.
Marquis-Nicholson R; Prosser DO; Love JM; Zhang L; Hayes I; George AM; Crawford JR; Skinner JR; Love DR
Circ Cardiovasc Genet; 2014 Feb; 7(1):17-22. PubMed ID: 24395924
[TBL] [Abstract][Full Text] [Related]
67. [Molecular genetic diagnostics of the cause of ventricular arrhythmias in children].
Brøndberg AK; Bjerre JV; Nielsen JC; Jensen HK
Ugeskr Laeger; 2015 Sep; 177(38):V04150366. PubMed ID: 26376421
[TBL] [Abstract][Full Text] [Related]
68. Clinical and neurophysiological variability in Andersen-Tawil syndrome.
Kokubun N; Aoki R; Nagashima T; Komagamine T; Kuroda Y; Horie M; Hirata K
Muscle Nerve; 2019 Dec; 60(6):752-757. PubMed ID: 31509255
[TBL] [Abstract][Full Text] [Related]
69. Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome.
Moreno-Manuel AI; Gutiérrez LK; Vera-Pedrosa ML; Cruz FM; Bermúdez-Jiménez FJ; Martínez-Carrascoso I; Sánchez-Pérez P; Macías Á; Jalife J
Cardiovasc Res; 2023 May; 119(4):919-932. PubMed ID: 35892314
[TBL] [Abstract][Full Text] [Related]
70. Electrophysiologic characteristics of an Andersen syndrome patient with KCNJ2 mutation.
Nagase S; Kusano KF; Yoshida M; Ohe T
Heart Rhythm; 2007 Apr; 4(4):512-5. PubMed ID: 17399643
[TBL] [Abstract][Full Text] [Related]
71. Andersen-Tawil syndrome with early fixed myopathy.
Lefter S; Hardiman O; Costigan D; Lynch B; McConville J; Hand CK; Ryan AM
J Clin Neuromuscul Dis; 2014 Dec; 16(2):79-82. PubMed ID: 25415519
[TBL] [Abstract][Full Text] [Related]
72. Andersen's syndrome mutation effects on the structure and assembly of the cytoplasmic domains of Kir2.1.
Pegan S; Arrabit C; Slesinger PA; Choe S
Biochemistry; 2006 Jul; 45(28):8599-606. PubMed ID: 16834334
[TBL] [Abstract][Full Text] [Related]
73. Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7).
Tsuboi M; Antzelevitch C
Heart Rhythm; 2006 Mar; 3(3):328-35. PubMed ID: 16500306
[TBL] [Abstract][Full Text] [Related]
74. Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression.
Miake J; Marbán E; Nuss HB
J Clin Invest; 2003 May; 111(10):1529-36. PubMed ID: 12750402
[TBL] [Abstract][Full Text] [Related]
75. Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndrome.
Bendahhou S; Donaldson MR; Plaster NM; Tristani-Firouzi M; Fu YH; Ptácek LJ
J Biol Chem; 2003 Dec; 278(51):51779-85. PubMed ID: 14522976
[TBL] [Abstract][Full Text] [Related]
76. A family with Andersen-Tawil syndrome and dilated cardiomyopathy.
Schoonderwoerd BA; Wiesfeld AC; Wilde AA; van den Heuvel F; Van Tintelen JP; van den Berg MP; Van Veldhuisen DJ; Van Gelder IC
Heart Rhythm; 2006 Nov; 3(11):1346-50. PubMed ID: 17074642
[No Abstract] [Full Text] [Related]
77. 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]
78. Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen-Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT).
Tully I; Atherton J; Hunt L; Ingles J; Semsarian C; McGaughran J
Int J Cardiol; 2015 Dec; 201():473-5. PubMed ID: 26322597
[No Abstract] [Full Text] [Related]
79. Modeling of IK1 mutations in human left ventricular myocytes and tissue.
Seemann G; Sachse FB; Weiss DL; Ptácek LJ; Tristani-Firouzi M
Am J Physiol Heart Circ Physiol; 2007 Jan; 292(1):H549-59. PubMed ID: 16936001
[TBL] [Abstract][Full Text] [Related]
80. 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]
[Previous] [Next] [New Search]
