| Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle … T Arimura, A Helbling-Leclerc, C Massart, S Varnous, F Niel, E Lacene, ... Human molecular genetics 14 (1), 155-169, 2005 | 354 | 2005 |
| Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy T Hayashi, T Arimura, M Itoh-Satoh, K Ueda, S Hohda, N Inagaki, ... Journal of the American College of Cardiology 44 (11), 2192-2201, 2004 | 353 | 2004 |
| Titin mutations as the molecular basis for dilated cardiomyopathy M Itoh-Satoh, T Hayashi, H Nishi, Y Koga, T Arimura, T Koyanagi, ... Biochemical and biophysical research communications 291 (2), 385-393, 2002 | 337 | 2002 |
| Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy A Muchir, P Pavlidis, V Decostre, AJ Herron, T Arimura, G Bonne, ... The Journal of clinical investigation 117 (5), 1282-1293, 2007 | 322 | 2007 |
| Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia K Ueda, K Nakamura, T Hayashi, N Inagaki, M Takahashi, T Arimura, ... Journal of Biological Chemistry 279 (26), 27194-27198, 2004 | 307 | 2004 |
| Autophagic degradation of nuclear components in mammalian cells YE Park, YK Hayashi, G Bonne, T Arimura, S Noguchi, I Nonaka, I Nishino Autophagy 5 (6), 795-804, 2009 | 245 | 2009 |
| αB-crystallin mutation in dilated cardiomyopathy N Inagaki, T Hayashi, T Arimura, Y Koga, M Takahashi, H Shibata, ... Biochemical and biophysical research communications 342 (2), 379-386, 2006 | 242 | 2006 |
| A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C T Arimura, T Hayashi, H Terada, SY Lee, Q Zhou, M Takahashi, K Ueda, ... Journal of Biological Chemistry 279 (8), 6746-6752, 2004 | 196 | 2004 |
| Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations K Hinohara, T Nakajima, M Takahashi, S Hohda, T Sasaoka, K Nakahara, ... Journal of human genetics 53 (4), 357-359, 2008 | 190 | 2008 |
| Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy T Hayashi, T Arimura, K Ueda, H Shibata, S Hohda, M Takahashi, H Hori, ... Biochemical and biophysical research communications 313 (1), 178-184, 2004 | 186 | 2004 |
| Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations A Muchir, J Medioni, M Laluc, C Massart, T Arimura, AJVD Kooi, ... Muscle & nerve 30 (4), 444-450, 2004 | 179 | 2004 |
| Cardiac Ankyrin Repeat Protein Gene (ANKRD1) Mutations in Hypertrophic Cardiomyopathy T Arimura, JM Bos, A Sato, T Kubo, H Okamoto, H Nishi, H Harada, ... Journal of the American College of Cardiology 54 (4), 334-342, 2009 | 178 | 2009 |
| Endothelin‐1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy–induced pluripotent stem cell–derived cardiomyocytes A Tanaka, S Yuasa, G Mearini, T Egashira, T Seki, M Kodaira, ... Journal of the American Heart Association 3 (6), e001263, 2014 | 172 | 2014 |
| Dilated cardiomyopathy‐associated BAG3 mutations impair Z‐disc assembly and enhance sensitivity to apoptosis in cardiomyocytes T Arimura, T Ishikawa, S Nunoda, S Kawai, A Kimura Human mutation 32 (12), 1481-1491, 2011 | 165 | 2011 |
| ANKRD1, the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene M Moulik, M Vatta, SH Witt, AM Arola, RT Murphy, WJ McKenna, ... Journal of the American College of Cardiology 54 (4), 325-333, 2009 | 150 | 2009 |
| A novel disease gene for brugada syndrome: sarcolemmal membrane–associated protein gene mutations impair intracellular trafficking of hnav1. 5 T Ishikawa, A Sato, CA Marcou, DJ Tester, MJ Ackerman, L Crotti, ... Circulation: Arrhythmia and Electrophysiology 5 (6), 1098-1107, 2012 | 123 | 2012 |
| Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations E Purevjav, T Arimura, S Augustin, AC Huby, K Takagi, S Nunoda, ... Human molecular genetics 21 (9), 2039-2053, 2012 | 115 | 2012 |
| Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy H Otsuka, T Arimura, T Abe, H Kawai, Y Aizawa, T Kubo, H Kitaoka, ... Circulation Journal 76 (2), 453-461, 2012 | 110 | 2012 |
| Structural analysis of obscurin gene in hypertrophic cardiomyopathy T Arimura, Y Matsumoto, O Okazaki, T Hayashi, M Takahashi, N Inagaki, ... Biochemical and biophysical research communications 362 (2), 281-287, 2007 | 106 | 2007 |
| Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis E Purevjav, J Varela, M Morgado, DL Kearney, H Li, MD Taylor, T Arimura, ... Journal of the American College of Cardiology 56 (18), 1493-1502, 2010 | 105 | 2010 |
