Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Ryo, Inuzuka"'
Autor:
Keiichi Hirono, Yukiko Hata, Teruhiko Imamura, Kaori Tsuboi, Shinya Takarada, Mako Okabe, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Shojiro Ichimata, Naoki Nishida, Hidenori Iwasaki, Susumu Urata, Seigo Okada, Tomoya Hiratsuji, Heima Sakaguchi, Kiyohiro Takigiku, Makoto Nakazawa, Eiki Nishihara, Masako Harada, Osamu Matsuo, Kenji Yasuda, Yoko Yoshida, Hidemasa Namiki, Kazushi Yasuda, Toshinobu Ifuku, Kotaro Urayama, Hideharu Oka, Kayo Ogino, Akio Kato, Nobuhiko Kan, Shunji Seki, Mitsuru Seki, Yutaka Odanaka, Satoru Iwashima, Shuichiro Yoshida, Toyohisa Miyata, Tomoyuki Miyamoto, Ken Watanabe, Naoki Kuwabara, Ryo Inuzuka, Yoshihiro Takahashi, Hisanori Sakazaki, Jun Muneuchi, Shigetoyo Kogaki, Fujito Numano, Sachiko Kido, Masaki Nii, Shinsuke Hoshino, Hidekazu Ishida, Jun Maeda, Yasunobu Hayabuchi, Yoshikazu Otsubo, Kazuyuki Ikeda, Shinya Tsukano, Makoto Watanabe, Nobuo Momoi, Takanari Fujii, Tao Fujioka, Mitsuhiro Fujino, Hiroki Uchiyama, Shigehito Baba, Hitoshi Horigome, Takashi Honda, Kazutaka Suzuki, Fukiko Ichida
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 21 (2024)
Background Left ventricular noncompaction (LVNC) is a hereditary type of cardiomyopathy characterized by prominent trabeculations. Detailed characteristics of biventricular noncompaction (BiVNC) remain unknown. This study aimed to elucidate the clini
Externí odkaz:
https://doaj.org/article/0f80e1600f4e43fb837026a73925f862
Autor:
Satoshi Ishii, Takayuki Fujiwara, Hiroki Yagi, Norifumi Takeda, Masahiko Ando, Haruo Yamauchi, Ryo Inuzuka, Yuki Taniguchi, Masaru Hatano, Issei Komuro
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Objective Loeys–Dietz syndrome (LDS) is a heritable disorder of connective tissue closely related to Marfan syndrome (MFS). LDS is caused by loss‐of‐function variants of genes that encode components of transforming growth factor‐β (
Externí odkaz:
https://doaj.org/article/82f79ac17a6b40dabb45add826366cfc
Autor:
Shun Kawai, Kyongsun Pak, Shintaro Iwamoto, Chihiro Kawakami, Ryo Inuzuka, Jun Maeda, Yoshiyuki Furutani, Mitsuhiro Kamisago, Shunichi Takatsuki, Tomomi Uyeda, Hiroyuki Yamagishi, Shuichi Ito, Tohru Kobayashi
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 17 (2023)
Background Many prenatal factors are reported to be associated with congenital heart defects (CHD) in offspring. However, these associations have not been adequately examined using large‐scale birth cohorts. Methods and Results We evaluated a data
Externí odkaz:
https://doaj.org/article/0ecc0f09ada4412f87aba87613e3d854
Autor:
Hiroki Yagi, Hiroshi Takiguchi, Norifumi Takeda, Ryo Inuzuka, Yuki Taniguchi, Kristine Joyce Porto, Hiroyuki Ishiura, Jun Mitsui, Hiroyuki Morita, Issei Komuro
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract Congenital contractural arachnodactyly (CCA) is caused by pathogenic FBN2 variants; however, the contributions of copy number variations (CNVs) to CCA are still unknown. Here, we report on a familial case of CCA, in which a novel multiexon d
Externí odkaz:
https://doaj.org/article/625ec588b80e40d9940d87d25c621beb
Autor:
Kaname Sato, Koichi Takamizawa, Yosuke Ogawa, Yu Tanaka, Kazuhiro Shiraga, Hitomi Masuda, Hikoro Matsui, Ryo Inuzuka, Hideaki Senzaki
Publikováno v:
American Journal of Physiology: Heart & Circulatory Physiology; Mar2024, Vol. 326 Issue 3, pH812-H820, 9p
Autor:
Hajime Abe, Norihiko Takeda, Takayuki Isagawa, Hiroaki Semba, Satoshi Nishimura, Masaki Suimye Morioka, Yu Nakagama, Tatsuyuki Sato, Katsura Soma, Katsuhiro Koyama, Masaki Wake, Manami Katoh, Masataka Asagiri, Michael L. Neugent, Jung-whan Kim, Christian Stockmann, Tomo Yonezawa, Ryo Inuzuka, Yasushi Hirota, Koji Maemura, Takeshi Yamashita, Kinya Otsu, Ichiro Manabe, Ryozo Nagai, Issei Komuro
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Fibrosis is a hallmark of several cardiac pathologies and its underlying mechanisms are still poorly defined. Here the authors show that macrophage hypoxia signaling following transverse aortic constriction in mice suppresses the activation of cardia
Externí odkaz:
https://doaj.org/article/71dda70f0fa943e6abde76eae9ef37b9
Autor:
Atsushi, Yao, Ryo, Inuzuka, Atsushi, Mizuno, Hiroyuki, Iwano, Shunsuke, Tatebe, Yasumasa, Tsukamoto, Ichiro, Sakamoto, Hiroyuki, Watanabe, Nobuyuki, Fukuda, Fumie, Takechi, Shiro, Adachi, Yusuke, Akazawa, Koichiro, Kuwahara, Kaoru, Dohi, Tomoko, Ishizu, Makoto, Miyake, Norimichi, Koitabashi, Saki, Hasegawa-Tamba, Seiichi, Sato, Takanari, Fujii, Eiji, Ehara, Tohru, Minamino, Hirotsugu, Yamada, Eiji, Yamashita, Naoto, Kawamatsu, Keita, Masuda, Katsura, Soma, Isao, Shiraishi, Ryozo, Nagai, Koichiro, Niwa
Publikováno v:
Journal of Cardiology. 80(6):525-531
BackgroundThe Japanese Network of Cardiovascular Departments for Adult Congenital Heart Disease (JNCVD-ACHD) was founded in 2011 for the lifelong care of adult patients with congenital heart disease (ACHD patients). This network maintains the first J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf379bfc8b63d4cf79a6387f1abd476c
http://hdl.handle.net/10295/00006148
http://hdl.handle.net/10295/00006148
Autor:
Yu Nakagama, Norihiko Takeda, Seishi Ogawa, Hiroyuki Takeda, Yoshiyuki Furutani, Toshio Nakanishi, Tatsuyuki Sato, Yoichiro Hirata, Akira Oka, Ryo Inuzuka
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Variants in the LZTR1 (leucine‐zipper‐like transcription regulator 1) gene (OMIM #600574) have been reported in recessive Noonan syndrome patients. In vivo evidence from animal models to support its causative role is lacking.
Externí odkaz:
https://doaj.org/article/a35ab36eda294c3c9d21f00b20f0a5de
Autor:
Takako Takano, Michio Akagi, Haruyoshi Takaki, Ryo Inuzuka, Yoshitsugu Nogimori, Hiroshi Ono, Masahide Kaneko, Norifumi Hagiwara
Publikováno v:
BMJ Paediatrics Open, Vol 3, Iss 1 (2019)
Reports indicate lower Down syndrome (DS) survival among females than among males in Australia, contrasting with female longevity in the general population. Using data on 1310 people with DS (626 females and 684 males) in Japan from five hospitals’
Externí odkaz:
https://doaj.org/article/e3baecbf32bd4490983a9cf0bcca13bb
Autor:
Ryo, Inuzuka, Hisateru, Tachimori, Sung-Hae, Kim, Hikoro, Matsui, Tohru, Kobayashi, Atsuko, Kato, Takanari, Fujii, Mami, Ho, Hanako, Morikawa, Sara, Takahashi, Haruki, Shirato, Yuji, Haishima, Yoshihiro, Okamoto, Hideyuki, Sakoda, Hideshi, Tomita
Publikováno v:
Circulation Journal. 86:1990-1997
Balloon atrial septostomy (BAS) is an essential catheterization procedure for congenital heart lesions. Recently, a balloon catheter for static BAS was approved for the first time in Japan as an alternative to the conventional pull-through BAS. Despi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b7ed9c4646853d71e997b97262d7392
https://doi.org/10.1253/circj.cj-22-0185
https://doi.org/10.1253/circj.cj-22-0185