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Titin mutations as the molecular basis for dilated cardiomyopathy.
Itoh-Satoh M, Hayashi T, Nishi H, Koga Y, Arimura T, Koyanagi T, Takahashi M, Hohda S, Ueda K, Nouchi T, Hiroe M, Marumo F, Imaizumi T, Yasunami M, Kimura A. Itoh-Satoh M, et al. Among authors: ueda k. Biochem Biophys Res Commun. 2002 Feb 22;291(2):385-93. doi: 10.1006/bbrc.2002.6448. Biochem Biophys Res Commun. 2002. PMID: 11846417
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy.
Hayashi T, Arimura T, Itoh-Satoh M, Ueda K, Hohda S, Inagaki N, Takahashi M, Hori H, Yasunami M, Nishi H, Koga Y, Nakamura H, Matsuzaki M, Choi BY, Bae SW, You CW, Han KH, Park JE, Knöll R, Hoshijima M, Chien KR, Kimura A. Hayashi T, et al. Among authors: ueda k. J Am Coll Cardiol. 2004 Dec 7;44(11):2192-201. doi: 10.1016/j.jacc.2004.08.058. J Am Coll Cardiol. 2004. PMID: 15582318 Free article.
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. 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
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. Among authors: ueda k. Int J Cardiol. 2005 Mar 18;99(2):343-5. doi: 10.1016/j.ijcard.2003.11.050. Int J Cardiol. 2005. PMID: 15749201
5,565 results