Zobrazeno 1 - 10
of 241
pro vyhledávání: '"Hiroki, Maruyama"'
Autor:
Akiko Jitsuhiro, Tomoki Maeda, Akiko Ogawa, Sayuri Yamada, Yuki Konoeda, Hiroki Maruyama, Fuyuaki Endo, Midori Kitagawa, Keishi Tanimoto, Atsushi Hotta, Toshikazu Tsuji
Publikováno v:
ACS Omega, Vol 9, Iss 8, Pp 9803-9812 (2024)
Externí odkaz:
https://doaj.org/article/c30ab086d55646819ad3a8dda5765f1b
Autor:
Keiko Tanaka, Hitoshi Sugiyama, Hiroshi Morinaga, Akifumi Onishi, Katsuyuki Tanabe, Haruhito A. Uchida, Hiroki Maruyama, Jun Wada
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Fabry disease (FD) is an X-linked disorder resulting in a deficiency of α-galactosidase A (GLA) activity. The R112H mutation of GLA is relatively common in Japanese FD patients, characterized by a late-onset phenotype, almost normal to mild lyso-Gb3
Externí odkaz:
https://doaj.org/article/dc24f115485b46959a505e0bd122c687
Autor:
Hiroki Maruyama, Taku Yamagata, Yoshihide Kanno, Takeshi Shimizu, Takuho Itasaka, Fumiyoshi Fujishima, Takashi Sawai, Kei Ito
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2024 (2024)
A 75-year-old female was diagnosed with a type 0-I, moderately differentiated, early gastric carcinoma on the posterior wall of the middle gastric body during esophagogastroduodenoscopy (EGD). Several small whitish structures, referred to as white gl
Externí odkaz:
https://doaj.org/article/d09ba32a0ae5480fbc613d8da1d2878f
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 34, Iss , Pp 100952- (2023)
Fabry disease (FD) is an inherited disease caused by deficient α-galactosidase A activity that is characterized by the accumulation of globotriaosylceramide (Gb3) and globotriaosylsphingosine (lyso-Gb3). Although plasma lyso-Gb3 is a sensitive bioma
Externí odkaz:
https://doaj.org/article/38dab95368984adf9cc969b76835e9a4
Autor:
Hiroki Maruyama, Atsumi Taguchi, Mariko Mikame, Atsushi Izawa, Naoki Morito, Kazufumi Izaki, Toshiyuki Seto, Akifumi Onishi, Hitoshi Sugiyama, Norio Sakai, Kenji Yamabe, Yukio Yokoyama, Satoshi Yamashita, Hiroshi Satoh, Shigeru Toyoda, Michihiro Hosojima, Yumi Ito, Ryushi Tazawa, Satoshi Ishii
Publikováno v:
Current Issues in Molecular Biology, Vol 43, Iss 1, Pp 389-404 (2021)
Fabry disease is an X-linked disorder of α-galactosidase A (GLA) deficiency. Our previous interim analysis (1 July 2014 to 31 December 2015) revealed plasma globotriaosylsphingosine as a promising primary screening biomarker for Fabry disease proban
Externí odkaz:
https://doaj.org/article/b772c007d4b741eca470f621bcdfd666
Autor:
Hiroki Maruyama, Atsumi Taguchi, Mariko Mikame, Hongmei Lu, Norihiro Tada, Muneaki Ishijima, Haruka Kaneko, Mariko Kawai, Sawako Goto, Akihiko Saito, Riuko Ohashi, Yuji Nishikawa, Satoshi Ishii
Publikováno v:
FASEB BioAdvances, Vol 2, Iss 6, Pp 365-381 (2020)
Abstract Low bone mineral density (BMD)—diagnosed as osteoporosis or osteopenia—has been reported as a new characteristic feature of Fabry disease; however, the mechanism underlying the development of low BMD is unknown. We previously revealed th
Externí odkaz:
https://doaj.org/article/fcee537cb437432cbb0f55503ce4611a
Autor:
Tanimul Alam, Hiroki Maruyama, Chun Li, Strahil Iv. Pastuhov, Paola Nix, Michael Bastiani, Naoki Hisamoto, Kunihiro Matsumoto
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
The molecular mechanism of axon regeneration after injury is poorly understood. Here the authors show that in C. elegans, the HIF-1 transcription factor induces ectopic synthesis of serotonin in severed ‘non-serotonergic’ neurons and that seroton
Externí odkaz:
https://doaj.org/article/df74211fbd2e45be8c4c87f6e1c01ced
Autor:
Mariko Kawai, Yohei Kataoka, Junya Sonobe, Hiromitsu Yamamoto, Hiroki Maruyama, Toshio Yamamoto, Kazuhisa Bessho, Kiyoshi Ohura
Publikováno v:
European Journal of Histochemistry, Vol 62, Iss 3 (2018)
Alveolar bone is not spontaneously regenerated following trauma or periodontitis. We previously proposed an animal model for new alveolar bone regeneration therapy based on the non-viral BMP-2/7 gene expression vector and in vivo electroporation, whi
Externí odkaz:
https://doaj.org/article/8f6321440fba48b99cbe0c5b4ea92467
Determination of cell fate in skeletal muscle following BMP gene transfer by in vivo electroporation
Autor:
Mariko Kawai, Yu-Ki Ohmori, Mai Nishino, Masayo Yoshida, Kaori Tabata, Do-Saku Hirota, Ayako Ryu-Mon, Hiromitsu Yamamoto, Junya Sonobe, Yo-Hei Kataoka, Noriko Shiotsu, Mika Ikegame, Hiroki Maruyama, Toshio Yamamoto, Kazuhisa Bessho, Kiyoshi Ohura
Publikováno v:
European Journal of Histochemistry, Vol 61, Iss 2 (2017)
We previously developed a novel method for gene transfer, which combined a non-viral gene expression vector with transcutaneous in vivo electroporation. We applied this method to transfer the bone morphogenetic protein (BMP) gene and induce ectopic b
Externí odkaz:
https://doaj.org/article/aa97c91d98f44c71b25bcb0733f9bfad
Publikováno v:
2022 27th OptoElectronics and Communications Conference (OECC) and 2022 International Conference on Photonics in Switching and Computing (PSC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d426def9c091f0c50c1b525af427651e
https://doi.org/10.23919/oecc/psc53152.2022.9849885
https://doi.org/10.23919/oecc/psc53152.2022.9849885