Kimura A - Search Results

1

A novel de novo mutation of β-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy.

Okada S, Suzuki Y, Arimura T, Kimura A, Narumi H, Hasegawa S. Okada S, et al. Among authors: kimura a. J Genet. 2014 Aug;93(2):557-60. doi: 10.1007/s12041-014-0414-8. J Genet. 2014. PMID: 25189259 No abstract available.

2

Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.

Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N. Ishikawa T, et al. Among authors: kimura a. Circ Arrhythm Electrophysiol. 2015 Apr;8(2):400-8. doi: 10.1161/CIRCEP.114.002534. Epub 2015 Feb 25. Circ Arrhythm Electrophysiol. 2015. PMID: 25717017 Free article.

3

Screening of sarcomere gene mutations in young athletes with abnormal findings in electrocardiography: identification of a MYH7 mutation and MYBPC3 mutations.

Kadota C, Arimura T, Hayashi T, Naruse TK, Kawai S, Kimura A. Kadota C, et al. Among authors: kimura a. J Hum Genet. 2015 Oct;60(10):641-5. doi: 10.1038/jhg.2015.81. Epub 2015 Jul 16. J Hum Genet. 2015. PMID: 26178432 Clinical Trial.

4

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy.

Arimura T, Bos JM, Sato A, Kubo T, Okamoto H, Nishi H, Harada H, Koga Y, Moulik M, Doi YL, Towbin JA, Ackerman MJ, Kimura A. Arimura T, et al. Among authors: kimura a. J Am Coll Cardiol. 2009 Jul 21;54(4):334-42. doi: 10.1016/j.jacc.2008.12.082. J Am Coll Cardiol. 2009. PMID: 19608031 Free article.

5

Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy.

Kubo T, Kitaoka H, Okawa M, Baba Y, Hirota T, Hayato K, Yamasaki N, Matsumura Y, Otsuka H, Arimura T, Kimura A, Doi YL. Kubo T, et al. Among authors: kimura a. Circ J. 2011;75(11):2654-9. doi: 10.1253/circj.cj-10-1314. Epub 2011 Jul 29. Circ J. 2011. PMID: 21799269 Free article. Clinical Trial.

6

Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy.

Otsuka H, Arimura T, Abe T, Kawai H, Aizawa Y, Kubo T, Kitaoka H, Nakamura H, Nakamura K, Okamoto H, Ichida F, Ayusawa M, Nunoda S, Isobe M, Matsuzaki M, Doi YL, Fukuda K, Sasaoka T, Izumi T, Ashizawa N, Kimura A. Otsuka H, et al. Among authors: kimura a. Circ J. 2012;76(2):453-61. doi: 10.1253/circj.cj-11-0876. Epub 2011 Nov 23. Circ J. 2012. PMID: 22112859 Free article.

7

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy.

Arimura T, Hayashi YK, Murakami T, Oya Y, Funabe S, Arikawa-Hirasawa E, Hattori N, Nishino I, Kimura A. Arimura T, et al. Among authors: kimura a. Circ J. 2009 Jan;73(1):158-61. doi: 10.1253/circj.cj-08-0722. Epub 2008 Nov 17. Circ J. 2009. PMID: 19015585 Free article.

8

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene.

Moulik M, Vatta M, Witt SH, Arola AM, Murphy RT, McKenna WJ, Boriek AM, Oka K, Labeit S, Bowles NE, Arimura T, Kimura A, Towbin JA. Moulik M, et al. Among authors: kimura a. J Am Coll Cardiol. 2009 Jul 21;54(4):325-33. doi: 10.1016/j.jacc.2009.02.076. J Am Coll Cardiol. 2009. PMID: 19608030 Free PMC article.

9

Structural analysis of obscurin gene in hypertrophic cardiomyopathy.

Arimura T, Matsumoto Y, Okazaki O, Hayashi T, Takahashi M, Inagaki N, Hinohara K, Ashizawa N, Yano K, Kimura A. Arimura T, et al. Among authors: kimura a. Biochem Biophys Res Commun. 2007 Oct 19;362(2):281-7. doi: 10.1016/j.bbrc.2007.07.183. Epub 2007 Aug 13. Biochem Biophys Res Commun. 2007. PMID: 17716621

10

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.

Hinohara K, Nakajima T, Takahashi M, Hohda S, Sasaoka T, Nakahara KI, Chida K, Sawabe M, Arimura T, Sato A, Lee BS, Ban JM, Yasunami M, Park JE, Izumi T, Kimura A. Hinohara K, et al. Among authors: kimura a. J Hum Genet. 2008;53(4):357-359. doi: 10.1007/s10038-008-0248-4. Epub 2008 Feb 9. J Hum Genet. 2008. PMID: 18264662

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