Zobrazeno 1 - 10
of 183
pro vyhledávání: '"Hisashi Oishi"'
Autor:
Toshikazu Watanabe, Takashi Hirama, Ken Onodera, Hirotsugu Notsuda, Hisashi Oishi, Hiromichi Niikawa, Kazuyoshi Imaizumi, Yoshinori Okada
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Interstitial lung disease (ILD) represents a heterogeneous group of lung disorders characterized by fibrotic lung tissue changes. In regions with severe donor shortages, single-lung transplantation (SLTx) is often preferred over b
Externí odkaz:
https://doaj.org/article/892534cc754c41a5aa095cac140a347e
Autor:
Fumiko Tomiyama, Takaya Suzuki, Tatsuaki Watanabe, Jun Miyanaga, Anna Suzuki, Takayasu Ito, Sho Murai, Yuyo Suzuki, Hiromichi Niikawa, Hisashi Oishi, Hirotsugu Notsuda, Yui Watanabe, Takashi Hirama, Ken Onodera, Takeo Togo, Masafumi Noda, Thomas K. Waddell, Golnaz Karoubi, Yoshinori Okada
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Whole lung engineering and the transplantation of its products is an ambitious goal and ultimately a viable solution for alleviating the donor-shortage crisis for lung transplants. There are several limitations currently impeding progress in
Externí odkaz:
https://doaj.org/article/52c96afc31ac441187e69c4ada4801ca
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Somatic mutations in MYCN have been identified across various tumors, playing pivotal roles in tumorigenesis, tumor progression, and unfavorable prognoses. Despite its established notoriety as an oncogenic driver, there is a growing interest in explo
Externí odkaz:
https://doaj.org/article/bc8e53e220204ef6910f36236a31c184
Autor:
Hirotsugu Notsuda, Fumiko Tomiyama, Ken Onodera, Tatsuaki Watanabe, Yui Watanabe, Hisashi Oishi, Hiromichi Niikawa, Chihiro Inoue, Hideki Ota, Masafumi Noda, Yoshinori Okada
Publikováno v:
The Egyptian Heart Journal, Vol 75, Iss 1, Pp 1-6 (2023)
Abstract Background Systemic-to-pulmonary artery shunt (SPAS) is a rare condition that can occur as a result of congenital heart disease or chronic pulmonary inflammation, occasionally leading to life-threatening hemoptysis. Computed tomography (CT)
Externí odkaz:
https://doaj.org/article/226fed3938ec4cf6a09e31c28ee07b24
Autor:
Asmaa Y. Ammar, Fatma M. Minisy, Hossam H. Shawki, Mohamed Mansour, Shabaan A. Hemeda, Abeer F. El Nahas, Ahmed H. Sherif, Hisashi Oishi
Publikováno v:
Biomedicines, Vol 12, Iss 5, p 1016 (2024)
Hypoxia is a condition in which tissues of the body do not receive sufficient amounts of oxygen supply. Numerous studies have elucidated the intricate roles of hypoxia and its involvement in both physiological and pathological conditions. This study
Externí odkaz:
https://doaj.org/article/e7b872cd20de4041b6f3585e36fde8ab
Autor:
Nahoko Fujimoto, Katsuya Nagaoka, Ichiro Tatsuno, Hisashi Oishi, Makoto Tomita, Tadao Hasegawa, Yasuhito Tanaka, Takahiro Matsumoto
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Ultraviolet (UV) irradiation offers an effective and convenient method for the disinfection of pathogenic microorganisms. However, UV irradiation causes protein and/or DNA damage; therefore, further insight into the performance of different
Externí odkaz:
https://doaj.org/article/9a26ff5864944881bd4da5f6dac59583
Autor:
Yosuke Nishio, Kohji Kato, Frederic Tran Mau-Them, Hiroshi Futagawa, Chloé Quélin, Saori Masuda, Antonio Vitobello, Shiomi Otsuji, Hossam H. Shawki, Hisashi Oishi, Christel Thauvin-Robinet, Toshiki Takenouchi, Kenjiro Kosaki, Yoshiyuki Takahashi, Shinji Saitoh
Publikováno v:
HGG Advances, Vol 4, Iss 4, Pp 100238- (2023)
Summary: MYCN, a member of the MYC proto-oncogene family, regulates cell growth and proliferation. Somatic mutations of MYCN are identified in various tumors, and germline loss-of-function variants are responsible for Feingold syndrome, characterized
Externí odkaz:
https://doaj.org/article/500afd5a9bde413c8c9a8ccf0d6652d9
Autor:
Hirofumi Watanabe, Fumiyoshi Fujishima, Toru Motoi, Yayoi Aoyama, Tetsuya Niihori, Masanobu Takahashi, Sho Umegaki, Hisashi Oishi, Hiroshi Tada, Ryo Ichinohasama, Hironobu Sasano
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-6 (2022)
Abstract Background Germline TP53 mutations have been frequently reported in patients with Li–Fraumeni syndrome (LFS), resulting in a predisposition to various malignancies. Mutations other than germline TP53 mutations can also cause LFS-associated
Externí odkaz:
https://doaj.org/article/f5fd271aa8af47869ff2081aab790de4
Autor:
Naoya Yamaguchi, Atsushi Suzuki, Aya Yoshida, Tatsushi Tanaka, Kohei Aoyama, Hisashi Oishi, Yuichiro Hara, Tomoo Ogi, Izuki Amano, Satomi Kameo, Noriyuki Koibuchi, Yasuhiro Shibata, Shinya Ugawa, Haruo Mizuno, Shinji Saitoh
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract SLC26A4 is a known iodide transporter, and is localized at the apical membrane of thyrocytes. Previously, we reported that SLC26A7 is also involved in iodide transport and that Slc26a7 is a novel causative gene for congenital hypothyroidism.
Externí odkaz:
https://doaj.org/article/e96f5e5bc5174803af6db215698f5947
Autor:
Takashi Hirama, Miki Akiba, Tatsuaki Watanabe, Yui Watanabe, Hirotsugu Notsuda, Hisashi Oishi, Hiromichi Niikawa, Yoshinori Okada
Publikováno v:
BMC Pulmonary Medicine, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background As lung transplantation (LTX) is a valuable treatment procedure for end-stage pulmonary disease, delayed referral to a transplant center should be avoided. We aimed to conduct a single-center analysis of the survival time after li
Externí odkaz:
https://doaj.org/article/16ec813a4810479a9d560315d217dc71