木村 彰方 業績リスト

2013年

Arimura T, Takeya R, Ishikawa T, Yamano T, Matsuo A, Tatsumi T, Nomura T, *Sumimoto H and *Kimura A.
Dilated cardiomyopathy-associated FHOD3 variant impairs the ability to induce activation of transcription factor SRF.
Circ J, 77, 2990-2996, 2013
Arimura T, Onoue K, Takahashi-Tanaka Y, Ishikawa T, Kuwahara M, Setou M, Shigenbu S, Yamaguchi K, Bertrand AT, Machida N, Takayama K, Fukusato M, Tanaka R, Somekawa T, Nakano T, Yamane Y, Kuba K, Imai Y, Saito N, Bonne G and *Kimura A.
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.
Cardiovasc Res, 99, 382-394, 2013
Crocini C, Arimura T, Reischmann S, Eder A, Braren I, Hansen A, Eschenhagen T, *Kimura A and *Carrier L.
Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue.
Basic Res Cardiol, 108, 349, 2013
Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N and *Kimura A.
Novel SCN3B mutation associated with Brugada syndrome affects intracellular trafficking and function of Nav1.5.
Circ J, 77, 959-967, 2013

2012年

Ishikawa T, Sato A, Marcou CA, Tester DJ, Ackerman MJ, Crotti L, Schwartz PJ, On YK, Park JE, Nakamura K, Hiraoka M, Nakazawa K, Sakurada H, Arimura T, *Makita N and *Kimura A.
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.
Circ Arrhythm Electrophysiol, 5, 1098-1107. 2012
Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Sato M, Hosaka Y, Fukae S, Chinushi M, Oda H, Okabe H, Kimura A, Maemura K, Watanabe I, Kamakura S, Aizawa Y, Shimizu W and Makita N.
Similarities and differences in genetic and clinical characteristics between early repolarization syndrome and Brugada syndrome.
Circ Arrhythm Electrophysiol, 5, e60-e61, 2012
Purevjav E, Arimura T, Augustin S, Huby A-C, Takagi K, Nunoda S, Kearney DL, Taylor MD, Terasaki F, Bos JM, Ommen SR, Shibata H, Takahashi M, Itoh-Satoh M, McKenna W, Murphy RT, Labeit S, Yamanaka Y, Machida N, Park JE, Alexander PMA, Weintraub RG, Kitaura Y, Ackerman MJ, Kimura A and Towbin JA.
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Hum Mol Genet., 21, 2039-2053, 2012
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 and Kimura A.
Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy.
Circ J., 76, 453-461, 2012

2011年

Arimura T, Ishikawa T, Nunoda S, Kawai S and Kimura A.
Dilated cardiomyopathy-associated BAG3 mutations impair the Z-disc assembly and enhance the sensitivity to apoptosis in cardiomyocytes.
Hum Mutat, 1481-1491, 2011
Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Sato M, Hosaka Y, Fukae S, Chinushi M, Oda H, Okabe H, Kimura A, Maemura K, Watanabe I, Kamakura S, Aizawa Y, Shimizu W and Makita N.
Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization.
Circ Arrhythm Electrophysiol., 4, 874-881, 2011
Takahashi M, Chen Z, Watanabe K, Kobayashi H, Nakajima T, Kimura A and Izumi Y.
Toll-like receptor 2 gene polymorphisms associated with aggressive periodontitis in Japanese.
Open Dent J., 5, 190-194, 2011
Kubo T, Kitaoka H, Okawa M, Baba Y, Hirota T, Hayato K, Yamasaki N, Matsumura Y, Otsuka H, Arimura T, Kimura A and Doi YL.
Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy.
Circ J., 75, 2654-2659, 2011
Kimura A.
Contribution of genetic factors to the pathogenesis of dilated cardiomyopathy: the cause of dilated cardiomyopathy: genetic or acquired? (genetic-side).
Circ J., 75, 1756-1765, 2011
Chen Z, Nakajima T, Inoue Y, Kudo T, Jibiki M, Iwai T and Kimura A.
A single nucleotide polymorphism in the 3’-untranslated region of MyD88 gene is associated with Buerger disease but not with Takayasu arteritis in Japanese.
J Hum Genet., 56, 545-547, 2011
和文総説
木村彰方
心筋症の発症機序から考える治療戦略
Cardiovascular Frontier 2(3):192-198, 2011
木村彰方
遺伝子異常から心筋症発症の分子機序
CARDIAC PRACTICE 22(3):201-207, 2011
木村彰方
冠動脈疾患(下)−診断と治療の進歩―遺伝子検査
日本臨床 69(S9):380-386, 2011
木村彰方
心筋症の遺伝子異常と分子病態
進歩する心臓研究-Tokyo Heart Journal- 16(2):7-15, 2011
木村彰方
肥大型心筋症の遺伝子診断と発症機序解明への多面的アプローチ
循環器内科 70(5):423-432, 2011
和文著書
木村彰方
第6章 病態・治療 循環器疾患のゲノム解析
血管生物医学事典(日本血管生物医学会 編) 461-463, 2011
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