285 related articles for article (PubMed ID: 16571646)
41. Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndrome.
Decher N; Renigunta V; Zuzarte M; Soom M; Heinemann SH; Timothy KW; Keating MT; Daut J; Sanguinetti MC; Splawski I
Cardiovasc Res; 2007 Sep; 75(4):748-57. PubMed ID: 17568571
[TBL] [Abstract][Full Text] [Related]
42. Efficacy and safety of flecainide for ventricular arrhythmias in patients with Andersen-Tawil syndrome with KCNJ2 mutations.
Miyamoto K; Aiba T; Kimura H; Hayashi H; Ohno S; Yasuoka C; Tanioka Y; Tsuchiya T; Yoshida Y; Hayashi H; Tsuboi I; Nakajima I; Ishibashi K; Okamura H; Noda T; Ishihara M; Anzai T; Yasuda S; Miyamoto Y; Kamakura S; Kusano K; Ogawa H; Horie M; Shimizu W
Heart Rhythm; 2015 Mar; 12(3):596-603. PubMed ID: 25496985
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen-Tawil syndrome patient.
Déri S; Borbás J; Hartai T; Hategan L; Csányi B; Visnyovszki Á; Madácsy T; Maléth J; Hegedűs Z; Nagy I; Arora R; Labro AJ; Környei L; Varró A; Sepp R; Ördög B
Cardiovasc Res; 2021 Jul; 117(8):1923-1934. PubMed ID: 32810216
[TBL] [Abstract][Full Text] [Related]
45. [A new type of periodic paralysis: Andersen-Tawil syndrome].
Pouget J
Bull Acad Natl Med; 2008 Nov; 192(8):1551-6; discussion 1556-7. PubMed ID: 19445372
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Exaggerated Mg2+ inhibition of Kir2.1 as a consequence of reduced PIP2 sensitivity in Andersen syndrome.
Ballester LY; Vanoye CG; George AL
Channels (Austin); 2007; 1(3):209-17. PubMed ID: 18690034
[TBL] [Abstract][Full Text] [Related]
48. Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred.
Bendahhou S; Fournier E; Gallet S; Ménard D; Larroque MM; Barhanin J
Hum Mol Genet; 2007 Apr; 16(8):900-6. PubMed ID: 17324964
[TBL] [Abstract][Full Text] [Related]
49. Extracellular Kir2.1
Cruz FM; Macías Á; Moreno-Manuel AI; Gutiérrez LK; Vera-Pedrosa ML; Martínez-Carrascoso I; Sánchez Pérez P; Ruiz Robles JM; Bermúdez-Jiménez FJ; Díaz-Agustín A; Martínez de Benito F; Arias-Santiago S; Braza-Boils A; Martín-Martínez M; Gutierrez-Rodríguez M; Bernal JA; Zorio E; Jiménez-Jaimez J; Jalife J
Circ Res; 2024 Apr; 134(8):e52-e71. PubMed ID: 38497220
[TBL] [Abstract][Full Text] [Related]
50. Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the
Onore ME; Picillo E; D'Ambrosio P; Morra S; Nigro V; Politano L
Biomolecules; 2024 Apr; 14(4):. PubMed ID: 38672523
[TBL] [Abstract][Full Text] [Related]
51. 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]
52. 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]
53. Management and treatment of Andersen-Tawil syndrome (ATS).
Sansone V; Tawil R
Neurotherapeutics; 2007 Apr; 4(2):233-7. PubMed ID: 17395133
[TBL] [Abstract][Full Text] [Related]
54. Andersen-Tawil syndrome: prospective cohort analysis and expansion of the phenotype.
Yoon G; Oberoi S; Tristani-Firouzi M; Etheridge SP; Quitania L; Kramer JH; Miller BL; Fu YH; Ptácek LJ
Am J Med Genet A; 2006 Feb; 140(4):312-21. PubMed ID: 16419128
[TBL] [Abstract][Full Text] [Related]
55. 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]
56. KCNJ2 variant of unknown significance reclassified as long QT syndrome causing ventricular fibrillation.
Obeyesekere MN; Klein GJ; Conacher S; Krahn AD
Can J Cardiol; 2011; 27(6):870.e11-3. PubMed ID: 21875779
[TBL] [Abstract][Full Text] [Related]
57. Altered stress stimulation of inward rectifier potassium channels in Andersen-Tawil syndrome.
Seebohm G; Strutz-Seebohm N; Ursu ON; Preisig-Müller R; Zuzarte M; Hill EV; Kienitz MC; Bendahhou S; Fauler M; Tapken D; Decher N; Collins A; Jurkat-Rott K; Steinmeyer K; Lehmann-Horn F; Daut J; Tavaré JM; Pott L; Bloch W; Lang F
FASEB J; 2012 Feb; 26(2):513-22. PubMed ID: 22002906
[TBL] [Abstract][Full Text] [Related]
58. Reversible Dilated Cardiomyopathy Caused by a High Burden of Ventricular Arrhythmias in Andersen-Tawil Syndrome.
Rezazadeh S; Guo J; Duff HJ; Ferrier RA; Gerull B
Can J Cardiol; 2016 Dec; 32(12):1576.e15-1576.e18. PubMed ID: 27789106
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. Identification of the KCNJ2 Mutation in a Korean Family with Andersen-Tawil Syndrome and Developmental Delay.
Kim NR; Jang JH; Jeon GW; Cho EH; Sin JB
Ann Clin Lab Sci; 2016; 46(1):110-3. PubMed ID: 26927354
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]