Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Masaharu Akiyama"'
Autor:
Mutsumi Koyama, Euido Nishijima, Takaya Honda, Chizuru Gonmori-Ohta, Takeaki Sasamoto, Katsuyuki Tanaka, Akira Watanabe, Tadashi Nakano, Masaharu Akiyama
Publikováno v:
BMC Ophthalmology, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Ocular manifestations are known for non-Hodgkin lymphoma, but are rare for Hodgkin lymphoma. We report a case of Vogt-Koyanagi-Harada (VKH) disease presenting as serous retinal detachment and uveitis in both eyes in a child underg
Externí odkaz:
https://doaj.org/article/726f0921fa5b4e5897c1288e8d1a8883
Autor:
Osamu Yamada DR., Masaharu Akiyama, Kiyotaka Kawauchi, Tomoko Adachi, Hisashi Yamada, Naotoshi Kanda, Eizo Aikawa
Publikováno v:
Cell Transplantation, Vol 12 (2003)
Leukemic stem cells that expressed endogenous telomerase activity were induced to show overexpression of exogenous hTERT and were analyzed for biological changes in order to assess the possible influence of telomerase gene therapy on the transplantat
Externí odkaz:
https://doaj.org/article/7c200968985f4d94a069967e70afc159
Autor:
Souichi Suenobu, Keita Terashima, Masaharu Akiyama, Tomoyo Oguri, Asako Watanabe, Masatoshi Sugeno, Mitsuo Higashimori, Karen So, Yoshihiro Nishida
Publikováno v:
Neuro-Oncology Advances.
Background Plexiform neurofibromas (PN) are a manifestation of neurofibromatosis type 1 (NF1) that may cause morbidity and impact health-related quality of life (HRQoL). Selumetinib (ARRY-142886, AZD6244) is an orally available, selective, mitogen-ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b080c66e4700158d268815a96b402f2
https://doi.org/10.1093/noajnl/vdad054
https://doi.org/10.1093/noajnl/vdad054
Autor:
Junko Takita, Seishi Ogawa, Satoru Miyano, Kenichiro Hata, Yukichi Tanaka, Masashi Sanada, Akira Oka, Hajime Hosoi, Tomoko Iehara, Chikako Kiyotani, Takao Deguchi, Tsuyoshi Ito, Akiko Inoue, Junya Fujimura, Masaharu Akiyama, Tomoaki Taguchi, Asahito Hama, Akihiro Iguchi, Motohiro Kato, Teppei Shimamura, Hiroko Tanaka, Kenichi Chiba, Tomoko Kawai, Yusuke Sato, Keisuke Kataoka, Hiromichi Suzuki, Nobuyuki Kakiuchi, Akira Yokoyama, Yoshikage Inoue, Misa Yoshida, Shunsuke Kimura, Yuichi Shiraishi, Yusuke Shiozawa, Masahiro Sekiguchi, Kenichi Yoshida, Masafumi Seki, Tomoya Isobe
Supplementary Tables S1-S13. Supplementary Table S1. Clinical information and the summary of experiments performed on each sample. Supplementary Table S2. List of genes and regions captured for targeted deep sequencing. Supplementary Table S3. dbSNP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aa0cad0ccba19162ababf800382a54f
https://doi.org/10.1158/0008-5472.22417488.v1
https://doi.org/10.1158/0008-5472.22417488.v1
Autor:
Junko Takita, Seishi Ogawa, Satoru Miyano, Kenichiro Hata, Yukichi Tanaka, Masashi Sanada, Akira Oka, Hajime Hosoi, Tomoko Iehara, Chikako Kiyotani, Takao Deguchi, Tsuyoshi Ito, Akiko Inoue, Junya Fujimura, Masaharu Akiyama, Tomoaki Taguchi, Asahito Hama, Akihiro Iguchi, Motohiro Kato, Teppei Shimamura, Hiroko Tanaka, Kenichi Chiba, Tomoko Kawai, Yusuke Sato, Keisuke Kataoka, Hiromichi Suzuki, Nobuyuki Kakiuchi, Akira Yokoyama, Yoshikage Inoue, Misa Yoshida, Shunsuke Kimura, Yuichi Shiraishi, Yusuke Shiozawa, Masahiro Sekiguchi, Kenichi Yoshida, Masafumi Seki, Tomoya Isobe
Pancreatoblastoma is a rare pediatric pancreatic malignancy for which the molecular pathogenesis is not understood. In this study, we report the findings of an integrated multiomics study of whole-exome and RNA sequencing as well as genome-wide copy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1293c09c84026b5d8126e1ff8c33bc99
https://doi.org/10.1158/0008-5472.c.6509859.v1
https://doi.org/10.1158/0008-5472.c.6509859.v1
Autor:
Junko Takita, Seishi Ogawa, Satoru Miyano, Kenichiro Hata, Yukichi Tanaka, Masashi Sanada, Akira Oka, Hajime Hosoi, Tomoko Iehara, Chikako Kiyotani, Takao Deguchi, Tsuyoshi Ito, Akiko Inoue, Junya Fujimura, Masaharu Akiyama, Tomoaki Taguchi, Asahito Hama, Akihiro Iguchi, Motohiro Kato, Teppei Shimamura, Hiroko Tanaka, Kenichi Chiba, Tomoko Kawai, Yusuke Sato, Keisuke Kataoka, Hiromichi Suzuki, Nobuyuki Kakiuchi, Akira Yokoyama, Yoshikage Inoue, Misa Yoshida, Shunsuke Kimura, Yuichi Shiraishi, Yusuke Shiozawa, Masahiro Sekiguchi, Kenichi Yoshida, Masafumi Seki, Tomoya Isobe
Supplementary Figures S1-S10. Supplementary Figure S1. Depths and coverages of targeted deep sequencing. Supplementary Figure S2. Sequencing coverages and numbers of mutations detected by WES. Supplementary Figure S3. Tumor subclonal populations in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67dd54190fcd8d1d79d631268dd92217
https://doi.org/10.1158/0008-5472.22417491
https://doi.org/10.1158/0008-5472.22417491
Autor:
Takeaki Sasamoto, Masashi Kurobe, Chizuru Gonmori‐Ohta, Katsuyuki Tanaka, Takaya Honda, Tetsuro Sugihara, Masaharu Akiyama
Publikováno v:
Pediatrics International. 65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21fd3f30ec8f48e6bb9f75165e6e7042
https://doi.org/10.1111/ped.15501
https://doi.org/10.1111/ped.15501
Autor:
Chizuru Gonmori‐Ohta, Tatsuya Hirotsu, Taku Gomi, Satoshi Matsushima, Yuichiro Nonaka, Masaharu Akiyama
Publikováno v:
Pediatrics International. 65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::698e8b1124f513db6dfd29938737ce3d
https://doi.org/10.1111/ped.15484
https://doi.org/10.1111/ped.15484
Autor:
Masatoshi Takagi, Hiroaki Goto, Yoko Terao, Daisuke Hasegawa, Seishi Ogawa, Tadashi Kumamoto, Kenichi Yoshida, Masaharu Akiyama, Takaya Honda, Masayoshi Yamaoka
Publikováno v:
International Journal of Hematology. 115:140-145
Hepatosplenic T-cell lymphoma (HSTCL) is a rare subtype of peripheral T-cell lymphoma that occurs most often in adolescents and young adults and is rare in children. Because of the aggressive clinical course, resistance to conventional chemotherapy a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::345a1946e810a558bf2bcfe1ed821c0f
https://doi.org/10.1007/s12185-021-03229-0
https://doi.org/10.1007/s12185-021-03229-0
Autor:
Chizuru Gonmori Ohta, Tatsuya Hirotsu, Taku Gomi, Satoshi Matsushima, Yuichiro Nonaka, Masaharu Akiyama
Developmental venous anomaly (DVA) is a venous malformation that is usually asymptomatic and rarely requires treatment. We report a case of a rare subtype DVA with arteriovenous shunt, presenting with headache, nausea, aphasia, and seizure in a 15-ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::467c14c7fb9e5adeae66cc2b1d68ca7f
https://doi.org/10.21203/rs.3.rs-1831304/v1
https://doi.org/10.21203/rs.3.rs-1831304/v1