Doi T - Search Results

1

Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome.

Makiyama T, Akao M, Haruna Y, Tsuji K, Doi T, Ohno S, Nishio Y, Kita T, Horie M. Makiyama T, et al. Among authors: doi t. Circ J. 2008 Oct;72(10):1705-6. doi: 10.1253/circj.cj-08-0508. Epub 2008 Sep 2. Circ J. 2008. PMID: 18762705 Free article.

2

KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillation.

Ohno S, Zankov DP, Ding WG, Itoh H, Makiyama T, Doi T, Shizuta S, Hattori T, Miyamoto A, Naiki N, Hancox JC, Matsuura H, Horie M. Ohno S, et al. Among authors: doi t. Circ Arrhythm Electrophysiol. 2011 Jun;4(3):352-61. doi: 10.1161/CIRCEP.110.959619. Epub 2011 Apr 14. Circ Arrhythm Electrophysiol. 2011. PMID: 21493962

3

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: doi t. 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.

4

A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation.

Makiyama T, Akao M, Shizuta S, Doi T, Nishiyama K, Oka Y, Ohno S, Nishio Y, Tsuji K, Itoh H, Kimura T, Kita T, Horie M. Makiyama T, et al. Among authors: doi t. J Am Coll Cardiol. 2008 Oct 14;52(16):1326-34. doi: 10.1016/j.jacc.2008.07.013. J Am Coll Cardiol. 2008. PMID: 18929244 Free article.

5

Clopidogrel resistance in Japanese patients scheduled for percutaneous coronary intervention.

Hoshino K, Horiuchi H, Tada T, Tazaki J, Nishi E, Kawato M, Ikeda T, Yamamoto H, Akao M, Furukawa Y, Shizuta S, Toma M, Tamura T, Saito N, Doi T, Ozasa N, Jinnai T, Takahashi K, Watanabe H, Yoshikawa Y, Nishimoto N, Ouchi C, Morimoto T, Kita T, Kimura T. Hoshino K, et al. Among authors: doi t. Circ J. 2009 Feb;73(2):336-42. doi: 10.1253/circj.cj-08-0559. Epub 2008 Dec 24. Circ J. 2009. PMID: 19106460 Free article. Clinical Trial.

6

Coronary risk factor profile and prognostic factors for young Japanese patients undergoing coronary revascularization.

Furukawa Y, Ehara N, Taniguchi R, Haruna Y, Ozasa N, Saito N, Doi T, Hoshino K, Tamura T, Shizuta S, Abe M, Toma M, Morimoto T, Teramukai S, Fukushima M, Kita T, Kimura T; CREDO-Kyoto Investigators. Furukawa Y, et al. Among authors: doi t. Circ J. 2009 Aug;73(8):1459-65. doi: 10.1253/circj.cj-08-1083. Epub 2009 Jun 16. Circ J. 2009. PMID: 19531902 Free article.

7

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. 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

8

Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry.

Nakajima K, Aiba T, Makiyama T, Nishiuchi S, Ohno S, Kato K, Yamamoto Y, Doi T, Shizuta S, Onoue K, Yagihara N, Ishikawa T, Watanabe I, Kawakami H, Oginosawa Y, Murakoshi N, Nogami A, Aonuma K, Saito Y, Kimura T, Yasuda S, Makita N, Shimizu W, Horie M, Kusano K. Nakajima K, et al. Among authors: doi t. Circ J. 2018 Oct 25;82(11):2707-2714. doi: 10.1253/circj.CJ-18-0339. Epub 2018 Aug 4. Circ J. 2018. PMID: 30078822 Free article. Clinical Trial.

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

10

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. Among authors: doi t. 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

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