Tsuji K - Search Results

1

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. Haruna Y, et al. Among authors: tsuji k. Hum Mutat. 2007 Feb;28(2):208. doi: 10.1002/humu.9483. Hum Mutat. 2007. PMID: 17221872

2

High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutations.

Makiyama T, Akao M, Tsuji K, Doi T, Ohno S, Takenaka K, Kobori A, Ninomiya T, Yoshida H, Takano M, Makita N, Yanagisawa F, Higashi Y, Takeyama Y, Kita T, Horie M. Makiyama T, et al. Among authors: tsuji k. J Am Coll Cardiol. 2005 Dec 6;46(11):2100-6. doi: 10.1016/j.jacc.2005.08.043. Epub 2005 Nov 4. J Am Coll Cardiol. 2005. PMID: 16325048 Free article.

3

Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.

Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M. Ohno S, et al. Among authors: tsuji k. Hum Mutat. 2009 Apr;30(4):557-63. doi: 10.1002/humu.20834. Hum Mutat. 2009. PMID: 19306396

4

A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndrome.

Doi T, Makiyama T, Morimoto T, Haruna Y, Tsuji K, Ohno S, Akao M, Takahashi Y, Kimura T, Horie M. Doi T, et al. Among authors: tsuji k. Circ Cardiovasc Genet. 2011 Jun;4(3):253-60. doi: 10.1161/CIRCGENETICS.110.958157. Epub 2011 Apr 14. Circ Cardiovasc Genet. 2011. PMID: 21493816

5

Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia.

Ai T, Fujiwara Y, Tsuji K, Otani H, Nakano S, Kubo Y, Horie M. Ai T, et al. Among authors: tsuji k. Circulation. 2002 Jun 4;105(22):2592-4. doi: 10.1161/01.cir.0000019906.35135.a3. Circulation. 2002. PMID: 12045162

6

Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 gene.

Tsuji K, Akao M, Ishii TM, Ohno S, Makiyama T, Takenaka K, Doi T, Haruna Y, Yoshida H, Nakashima T, Kita T, Horie M. Tsuji K, et al. J Mol Cell Cardiol. 2007 Mar;42(3):662-9. doi: 10.1016/j.yjmcc.2006.12.015. Epub 2007 Jan 5. J Mol Cell Cardiol. 2007. PMID: 17292394

7

N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome.

Ohno S, Zankov DP, Yoshida H, Tsuji K, Makiyama T, Itoh H, Akao M, Hancox JC, Kita T, Horie M. Ohno S, et al. Among authors: tsuji k. Heart Rhythm. 2007 Mar;4(3):332-40. doi: 10.1016/j.hrthm.2006.11.004. Epub 2006 Nov 10. Heart Rhythm. 2007. PMID: 17341399

8

Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome.

Sakaguchi T, Shimizu W, Itoh H, Noda T, Miyamoto Y, Nagaoka I, Oka Y, Ashihara T, Ito M, Tsuji K, Ohno S, Makiyama T, Kamakura S, Horie M. Sakaguchi T, et al. Among authors: tsuji k. J Cardiovasc Electrophysiol. 2008 Aug;19(8):794-9. doi: 10.1111/j.1540-8167.2008.01138.x. Epub 2008 Mar 26. J Cardiovasc Electrophysiol. 2008. PMID: 18373596

9

A novel mutation associated with Jervell and Lange-Nielsen syndrome in a Japanese family.

Ohno S, Kubota T, Yoshida H, Tsuji K, Makiyama T, Yamada S, Kuga K, Yamaguchi I, Kita T, Horie M. Ohno S, et al. Among authors: tsuji k. Circ J. 2008 May;72(5):687-93. doi: 10.1253/circj.72.687. Circ J. 2008. PMID: 18441444 Free article.

10

Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome.

Nagaoka I, Shimizu W, Itoh H, Yamamoto S, Sakaguchi T, Oka Y, Tsuji K, Ashihara T, Ito M, Yoshida H, Ohno S, Makiyama T, Miyamoto Y, Noda T, Kamakura S, Akao M, Horie M. Nagaoka I, et al. Among authors: tsuji k. Circ J. 2008 May;72(5):694-9. doi: 10.1253/circj.72.694. Circ J. 2008. PMID: 18441445 Free article.

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