Zobrazeno 1 - 10
of 197
pro vyhledávání: '"Akihiro, Sakurai"'
Autor:
Tomohiro Kubo, Yuki Ikeda, Joji Muramatu, Kazuma Ishikawa, Makoto Yoshida, Kazuharu Kukita, Masafumi Imamura, Shintaro Sugita, Akihiro Sakurai, Kohichi Takada
Publikováno v:
Cancer Reports, Vol 7, Iss 8, Pp n/a-n/a (2024)
ABSTRACT Background Pancreatic acinar cell carcinoma (PACC) is a rare pancreatic neoplasm. Recently, molecular analysis revealed that PACC shows a high frequency of the BRCA1/2 mutation and is likely to be considered a cancer associated with heredita
Externí odkaz:
https://doaj.org/article/778d21f955c741028022b713c2fc9e5c
Autor:
Tasuku Mariya, Aki Ishikawa, Miyako Mizukami, Yumi Tanaka, Kayano Komatsu, Sachiko Miyazaki, Aika Korai, Tsuyoshi Baba, Shinichi Ishioka, Tsuyoshi Saito, Akihiro Sakurai
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101300- (2024)
Externí odkaz:
https://doaj.org/article/18c2a34cefa0412983a05181d39620a1
Autor:
Koshiro Nishimoto, Noriaki Lukas Santo, Masato Yonamine, Kazuhiro Takekoshi, Go Kaneko, Suguru Shirotake, Hisayo Fukushima, Yoshitaka Okada, Masanori Yasuda, Akihiro Sakurai, Masafumi Oyama, Kento Kanao
Publikováno v:
IJU Case Reports, Vol 5, Iss 6, Pp 459-463 (2022)
Introduction Patients with multiple endocrine neoplasia type 2A (MEN2A) harboring a pathological variant in the RET gene are characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and hyperparathyroidism. Although pheochromocytoma is c
Externí odkaz:
https://doaj.org/article/899c5a85e21f41b8a5da5515c2258062
Autor:
Kohichi Takada, Tomohiro Kubo, Junko Kikuchi, Makoto Yoshida, Ayako Murota, Yohei Arihara, Hajime Nakamura, Hiroyuki Nagashima, Hiroki Tanabe, Shintaro Sugita, Yumi Tanaka, Ayana Miura, Yoshihito Ohhara, Atsushi Ishiguro, Hiroshi Yokouchi, Yasuyuki Kawamoto, Yusuke Mizukami, Hirofumi Ohnishi, Ichiro Kinoshita, Akihiro Sakurai
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Characterization of the genomic landscape of biliary tract cancer (BTC) may lead to applying genotype-matched therapy for patients with this disease. Evidence that comprehensive cancer genomic profiling (CGP) guides genotype-matched therapy to improv
Externí odkaz:
https://doaj.org/article/df2b89da346346549ed40aef2c396d98
Autor:
Norito Suzuki, Masashi Idogawa, Makoto Emori, Kazuyuki Murase, Yohei Arihara, Hajime Nakamura, Makoto Usami, Tomohiro Kubo, Ichiro Kinoshita, Shintaro Sugita, Takashi Tokino, Tadashi Hasegawa, Akihiro Sakurai, Kohichi Takada
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 15, p2215-2219, 5p
Autor:
Kazuhiro Fukami, Akihiro Sakurai, Takamitsu Tsujimoto, Masaki Yamagami, Atsushi Kitada, Kota Morimoto, Kiho Nishioka, Shuji Nakanishi, Yusuke Yoshikane, Toshimitsu Nagao, Jun-ichi Katayama, Kuniaki Murase
Publikováno v:
Electrochemistry Communications, Vol 136, Iss , Pp 107238- (2022)
It is well-known that the electrodeposition of lithium usually results in the formation of dendrites on the electrode surface. This limits the utilization of metallic lithium as a material for, for example, the negative electrodes of rechargeable bat
Externí odkaz:
https://doaj.org/article/f27688a707d24facac1429e5d68bd23c
Autor:
Louise Vølund Larsen, Delphine Mirebeau-Prunier, Tsuneo Imai, Cristina Alvarez-Escola, Kornelia Hasse-Lazar, Simona Censi, Luciana A Castroneves, Akihiro Sakurai, Minoru Kihara, Kiyomi Horiuchi, Véronique Dorine Barbu, Francoise Borson-Chazot, Anne-Paule Gimenez-Roqueplo, Pascal Pigny, Stephane Pinson, Nelson Wohllk, Charis Eng, Berna Imge Aydogan, Dhananjaya Saranath, Sarka Dvorakova, Frederic Castinetti, Attila Patocs, Damijan Bergant, Thera P Links, Mariola Peczkowska, Ana O Hoff, Caterina Mian, Trisha Dwight, Barbara Jarzab, Hartmut P H Neumann, Mercedes Robledo, Shinya Uchino, Anne Barlier, Christian Godballe, Jes Sloth Mathiesen
Publikováno v:
Endocrine Connections, Vol 9, Iss 6, Pp 489-497 (2020)
Objective: Multiple endocrine neoplasia type 2A (MEN 2A) is a rare syndrome caused by RET germline mutations and has been associated with primary hyperparathyroidism (PHPT) in up to 30% of cases. Recommendations on RET screening in patients with appa
Externí odkaz:
https://doaj.org/article/fce9b24b992c46119c9143129797252c
Autor:
Shiori Ogawa, Tasuku Mariya, Yuya Fujibe, Marie Ogawa, Keiko Ikeda, Miyako Mizukami, Yoshika Kuno, Aki Ishikawa, Shinichi Ishioka, Akihiro Sakurai, Tsuyoshi Saito
Publikováno v:
Case Reports in Women's Health, Vol 33, Iss , Pp e00384- (2022)
Ehlers-Danlos syndrome is a rare genetic disorder that presents with a variety of pathologies depending on the disease type. Among them, vascular Ehlers-Danlos syndrome requires extremely careful management as there have been many reports of fatal pe
Externí odkaz:
https://doaj.org/article/104ad04baba244e999718cb2cb9b0dbb
Autor:
Tasuku Mariya, Yui Shichiri, Takeshi Sugimoto, Rie Kawamura, Syunsuke Miyai, Hidehito Inagaki, Eiji Sugihara, Keiko Ikeda, Tsuyoshi Baba, Aki Ishikawa, Michiko Ammae, Yoshiharu Nakaoka, Tsuyoshi Saito, Akihiro Sakurai, Hiroki Kurahashi
Publikováno v:
Prenatal Diagnosis. 43:304-313
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88848ec6740fa5eb97b1f1f6a4c1e539
https://doi.org/10.1002/pd.6334
https://doi.org/10.1002/pd.6334
Autor:
Satoru Yoshida, Hanayuki Okura, Hidetaka Suga, Tomohiko Nishitomi, Akihiro Sakurai, Hiroshi Arima, Akifumi Matsuyama
Publikováno v:
Stem Cell Research, Vol 46, Iss , Pp 101846- (2020)
We generated three disease-specific iPSC lines from a Multiple endocrine neoplasia type 1 (MEN1) patient and three control iPSC lines from an unaffected blood relative of the patient using unutilized lymphoblastoid B cell lines (LCLs) as a cell resou
Externí odkaz:
https://doaj.org/article/74945c5b08fd4fdea4822966e7374199