Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Tetsuo Konno"'
Autor:
Ronny Alcalai, Michael Arad, Hiroko Wakimoto, Dor Yadin, Joshua Gorham, Libin Wang, Elia Burns, Barry J. Maron, William C. Roberts, Tetsuo Konno, David A. Conner, Antonio R. Perez‐Atayde, Jon G. Seidman, Christine E. Seidman
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 17 (2021)
Background Human mutations in the X‐linked lysosome‐associated membrane protein‐2 (LAMP2) gene can cause a multisystem Danon disease or a primary cardiomyopathy characterized by massive hypertrophy, conduction system abnormalities, and malignan
Externí odkaz:
https://doaj.org/article/beaa5a868d0a4b8aa541598c15edec0b
Autor:
Yoji Nagata, Masakazu Yamagishi, Tetsuo Konno, Chiaki Nakanishi, Yoshihiro Asano, Shin Ito, Yuri Nakajima, Osamu Seguchi, Noboru Fujino, Masa-aki Kawashiri, Seiji Takashima, Masafumi Kitakaze, Kenshi Hayashi
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-1 (2018)
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.
Externí odkaz:
https://doaj.org/article/c3bfa9cd668240b2941789206f860cca
Autor:
Tetsuo Konno, Kenshi Hayashi, Noboru Fujino, Yoji Nagata, Akihiko Hodatsu, Eiichi Masuta, Kenji Sakata, Hiroyuki Nakamura, Masa-aki Kawashiri, Masakazu Yamagishi
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e101465 (2014)
BACKGROUND: Myocardial scarring can be assessed by cardiac magnetic resonance imaging with late gadolinium enhancement and by endomyocardial biopsy. However, accuracy of late gadolinium enhancement for predicting microscopic myocardial scarring in bi
Externí odkaz:
https://doaj.org/article/17e8df906bf941e0ae5714305e149dba
Autor:
Aiji Sakamoto, Masaaki Kawashiri, Hatsue Ishibashi-Ueda, Yuka Sugamoto, Tsuyoshi Yoshimuta, Takeo Higashikata, Hitoshi Ogino, Hayato Tada, Tetsuo Konno, Kenshi Hayashi, Masakazu Yamagishi
Publikováno v:
International Journal of Vascular Medicine, Vol 2012 (2012)
We examined the expression of ephrin-B1 and its cognate receptor EphB2, key regulators of angiogenesis and embryogenesis, in human abdominal aortic aneurysm (AAA) and analyzed their functional roles in cell migration. From 10 patients (9 males and 1
Externí odkaz:
https://doaj.org/article/e59eb1f5a77947c8a480c2f138733651
Autor:
Seiji Takashima, Noboru Fujino, Tetsuo Konno, Masakazu Yamagishi, Masa-aki Kawashiri, Atsuko Imai-Okazaki, Akihiko Hodatsu, Osamu Seguchi, Kenshi Hayashi, Masafumi Kitakaze, Osamu Tsukamoto, Satoru Yamazaki, Yuki Uyama, Yoshihiro Asano
Publikováno v:
ESC Heart Failure
Aims Cardiac myosin light chain kinase (cMLCK) phosphorylates ventricular myosin regulatory light chain 2 (MLC2v) and regulates sarcomere and cardiomyocyte organization. However, few data exist regarding the relationship between cMLCK mutations and M
Autor:
Toyonobu Tsuda, Noboru Fujino, Ryota Teramoto, Akihiro Nomura, Hayato Tada, Tetsuo Konno, Masakazu Yamagishi, Akihiko Hodatsu, Masa-aki Kawashiri, Chiaki Nakanishi, Shohei Yoshida, Yoshihiro Tanaka, Kenshi Hayashi, Yoji Nagata
Publikováno v:
Heart and Vessels. 34:159-166
Heterologous expression systems play a vital role in the characterization of potassium voltage-gated channel subfamily H member 2 (KCNH2) gene mutations, such as E637K which is associated with long QT syndrome type 2 (LQT2). In vivo assays using zebr
Autor:
Kenshi Hayashi, Atsushi Nohara, Hiroshi Mabuchi, Hayato Tada, Akihiro Inazu, Masa-aki Kawashiri, Ryota Teramoto, Tetsuo Konno, Masakazu Yamagishi, Takuya Nakahashi
Publikováno v:
Atherosclerosis. 269:272-278
Background and aims Familial chylomicronemia syndrome is a rare autosomal recessive disorder leading to severe hypertriglyceridemia (HTG) due to mutations in lipoprotein lipase (LPL)-associated genes. Few data exist on the clinical features of the di
Autor:
Kenshi, Hayashi, Toyonobu, Tsuda, Akihiro, Nomura, Noboru, Fujino, Atsushi, Nohara, Kenji, Sakata, Tetsuo, Konno, Chiaki, Nakanishi, Hayato, Tada, Yoji, Nagata, Ryota, Teramoto, Yoshihiro, Tanaka, Masa-Aki, Kawashiri, Masakazu, Yamagishi, S, Ito
Publikováno v:
Circulation Journal. 82:1271-1278
BACKGROUND B-type natriuretic peptide (BNP) may be a predictor of stroke risk in patients with nonvalvular atrial fibrillation (NVAF); because heart failure is associated with the incidence of stroke in AF patients. However, limited data exist regard
Autor:
Kenshi Hayashi, Akihiko Hodatsu, Yoji Nagata, Toyonobu Tsuda, Masa-aki Kawashiri, Kenji Sakata, Takashi Fujita, Akihiro Nomura, Noboru Fujino, Ryota Teramoto, Tetsuo Konno, Masakazu Yamagishi, Yoshihiro Tanaka, Masayuki Takamura, Hiroshi Furusho
Publikováno v:
JACC: Clinical Electrophysiology. 3:1136-1142
Objectives This study sought to investigate whether the presence of J waves was associated with cardiac events in patients with hypertrophic cardiomyopathy (HCM). Background It has been uncertain whether the presence of J waves predicts life-threaten
Autor:
Akihiro Inazu, Kenji Sakata, Hiroshi Mabuchi, Tetsuo Konno, Hirofumi Okada, Masakazu Yamagishi, Masa-aki Kawashiri, Atsushi Nohara, Chiaki Nakanishi, Kenshi Hayashi, Hayato Tada, Toshinori Higashikata
Publikováno v:
Atherosclerosis. 265:225-230
Low-density lipoprotein (LDL) apheresis has been used to treat refractory hyperlipidemia such as familial hypercholesterolemia (FH). Evolocumab, a proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor used in clinical settings, can reduce L