Horie M - Search Results

1

Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells.

Yoshinaga D, Baba S, Makiyama T, Shibata H, Hirata T, Akagi K, Matsuda K, Kohjitani H, Wuriyanghai Y, Umeda K, Yamamoto Y, Conklin BR, Horie M, Takita J, Heike T. Yoshinaga D, et al. Among authors: horie m. Stem Cell Reports. 2019 Aug 13;13(2):394-404. doi: 10.1016/j.stemcr.2019.06.007. Epub 2019 Aug 1. Stem Cell Reports. 2019. PMID: 31378668 Free PMC article.

2

Characterization of a novel missense mutation in the pore of HERG in a patient with long QT syndrome.

Yoshida H, Horie M, Otani H, Takano M, Tsuji K, Kubota T, Fukunami M, Sasayama S. Yoshida H, et al. Among authors: horie m. J Cardiovasc Electrophysiol. 1999 Sep;10(9):1262-70. doi: 10.1111/j.1540-8167.1999.tb00304.x. J Cardiovasc Electrophysiol. 1999. PMID: 10517660

3

Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome.

Takenaka K, Ai T, Shimizu W, Kobori A, Ninomiya T, Otani H, Kubota T, Takaki H, Kamakura S, Horie M. Takenaka K, et al. Among authors: horie m. Circulation. 2003 Feb 18;107(6):838-44. doi: 10.1161/01.cir.0000048142.85076.a2. Circulation. 2003. PMID: 12591753 Clinical Trial.

4

Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.

Kobori A, Sarai N, Shimizu W, Nakamura Y, Murakami Y, Makiyama T, Ohno S, Takenaka K, Ninomiya T, Fujiwara Y, Matsuoka S, Takano M, Noma A, Kita T, Horie M. Kobori A, et al. Among authors: horie m. J Cardiovasc Electrophysiol. 2004 Feb;15(2):190-9. doi: 10.1046/j.1540-8167.2004.03212.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028050

5

Double SCN5A mutation underlying asymptomatic Brugada syndrome.

Yokoi H, Makita N, Sasaki K, Takagi Y, Okumura Y, Nishino T, Makiyama T, Kitabatake A, Horie M, Watanabe I, Tsutsui H. Yokoi H, et al. Among authors: horie m. Heart Rhythm. 2005 Mar;2(3):285-92. doi: 10.1016/j.hrthm.2004.11.022. Heart Rhythm. 2005. PMID: 15851320 Free article.

6

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: horie m. 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.

7

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: horie m. Hum Mutat. 2007 Feb;28(2):208. doi: 10.1002/humu.9483. Hum Mutat. 2007. PMID: 17221872

8

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: horie m. 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

9

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: horie m. 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

10

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: horie m. 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

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