Aizawa Y - Search Results

1

A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome.

Aizawa Y, Ueda K, Scornik F, Cordeiro JM, Wu Y, Desai M, Guerchicoff A, Nagata Y, Iesaka Y, Kimura A, Hiraoka M, Antzelevitch C. Aizawa Y, et al. J Cardiovasc Electrophysiol. 2007 Sep;18(9):972-7. doi: 10.1111/j.1540-8167.2007.00889.x. Epub 2007 Jul 26. J Cardiovasc Electrophysiol. 2007. PMID: 17655673 Free PMC article.

2

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.

Antzelevitch C, Pollevick GD, Cordeiro JM, Casis O, Sanguinetti MC, Aizawa Y, Guerchicoff A, Pfeiffer R, Oliva A, Wollnik B, Gelber P, Bonaros EP Jr, Burashnikov E, Wu Y, Sargent JD, Schickel S, Oberheiden R, Bhatia A, Hsu LF, Haïssaguerre M, Schimpf R, Borggrefe M, Wolpert C. Antzelevitch C, et al. Among authors: aizawa y. Circulation. 2007 Jan 30;115(4):442-9. doi: 10.1161/CIRCULATIONAHA.106.668392. Epub 2007 Jan 15. Circulation. 2007. PMID: 17224476 Free PMC article.

3

Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defect.

Aizawa Y, Ueda K, Wu LM, Inagaki N, Hayashi T, Takahashi M, Ohta M, Kawano S, Hirano Y, Yasunami M, Aizawa Y, Kimura A, Hiraoka M. Aizawa Y, et al. FEBS Lett. 2004 Sep 10;574(1-3):145-50. doi: 10.1016/j.febslet.2004.08.018. FEBS Lett. 2004. PMID: 15358555 Free article.

4

Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome.

Sato A, Arimura T, Makita N, Ishikawa T, Aizawa Y, Ushinohama H, Aizawa Y, Kimura A. Sato A, et al. Among authors: aizawa y. J Biol Chem. 2009 Dec 11;284(50):35122-33. doi: 10.1074/jbc.M109.017293. Epub 2009 Oct 13. J Biol Chem. 2009. PMID: 19825999 Free PMC article.

5

A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.

Ikrar T, Hanawa H, Watanabe H, Okada S, Aizawa Y, Ramadan MM, Komura S, Yamashita F, Chinushi M, Aizawa Y. Ikrar T, et al. Among authors: aizawa y. J Cardiovasc Electrophysiol. 2008 May;19(5):541-9. doi: 10.1111/j.1540-8167.2007.01076.x. Epub 2008 Feb 4. J Cardiovasc Electrophysiol. 2008. PMID: 18266681

6

Anti-KCNH2 antibody-induced long QT syndrome: novel acquired form of long QT syndrome.

Nakamura K, Katayama Y, Kusano KF, Haraoka K, Tani Y, Nagase S, Morita H, Miura D, Fujimoto Y, Furukawa T, Ueda K, Aizawa Y, Kimura A, Kurachi Y, Ohe T. Nakamura K, et al. Among authors: aizawa y. J Am Coll Cardiol. 2007 Oct 30;50(18):1808-9. doi: 10.1016/j.jacc.2007.07.037. J Am Coll Cardiol. 2007. PMID: 17964047 Free article. No abstract available.

7

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.

Ravn LS, Aizawa Y, Pollevick GD, Hofman-Bang J, Cordeiro JM, Dixen U, Jensen G, Wu Y, Burashnikov E, Haunso S, Guerchicoff A, Hu D, Svendsen JH, Christiansen M, Antzelevitch C. Ravn LS, et al. Among authors: aizawa y. Heart Rhythm. 2008 Mar;5(3):427-35. doi: 10.1016/j.hrthm.2007.12.019. Epub 2008 Feb 4. Heart Rhythm. 2008. PMID: 18313602 Free PMC article.

8

Role of HCN4 channel in preventing ventricular arrhythmia.

Ueda K, Hirano Y, Higashiuesato Y, Aizawa Y, Hayashi T, Inagaki N, Tana T, Ohya Y, Takishita S, Muratani H, Hiraoka M, Kimura A. Ueda K, et al. Among authors: aizawa y. J Hum Genet. 2009 Feb;54(2):115-21. doi: 10.1038/jhg.2008.16. Epub 2009 Jan 23. J Hum Genet. 2009. PMID: 19165230

9

Distinct Features of Probands With Early Repolarization and Brugada Syndromes Carrying SCN5A Pathogenic Variants.

Zhang ZH, Barajas-Martínez H, Xia H, Li B, Capra JA, Clatot J, Chen GX, Chen X, Yang B, Jiang H, Tse G, Aizawa Y, Gollob MH, Scheinman M, Antzelevitch C, Hu D. Zhang ZH, et al. Among authors: aizawa y. J Am Coll Cardiol. 2021 Oct 19;78(16):1603-1617. doi: 10.1016/j.jacc.2021.08.024. J Am Coll Cardiol. 2021. PMID: 34649698 Free PMC article.

10

A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardia.

Aizawa Y, Ueda K, Komura S, Washizuka T, Chinushi M, Inagaki N, Matsumoto Y, Hayashi T, Takahashi M, Nakano N, Yasunami M, Kimura A, Hiraoka M, Aizawa Y. Aizawa Y, et al. Int J Cardiol. 2005 Mar 18;99(2):343-5. doi: 10.1016/j.ijcard.2003.11.050. Int J Cardiol. 2005. PMID: 15749201

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