| ○ |
|
齋藤 加代子 |
東京女子医科大学臨床ゲノムセンター |
| 遺伝子医学、ゲノム医療 |
|
Kaneko K, Arakawa R, Urano M, Aoki R, Saito K. Relationships between long-term observations of motor milestones and genotype analysis results in childhood-onset Japanese spinal muscular atrophy patients. Brain & Development 2017;39:763-773 |
SMA診療マニュアル編集委員会（代表：齋藤加代子）編. 脊髄性筋萎縮症診療マニュアル,第１版. 金芳堂,京都,pp150,2012
|
|
Saito K, Arakawa R. Panel discussion - Spinal muscular atrophy - Japan experience, Launching a new era in spinal muscular atrophy treatment. 15th Asian and Oceanian Myology Center Annual Scientific Meeting 2016, 2016.5.26-29, Hsinchu, Taiwan.
|
|
| |
|
宮野 悟 |
東京大学医科学研究所・教授 |
| バイオインフォマティクス、がんゲノミクス |
Adaptive NetworkProfiler for Identifying Cancer Characteristic-Specific Gene Regulatory Networks. Park H, Shimamura T, Imoto S, Miyano S. J Comput Biol. 25(2):130-145, 2018.
|
| Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers. Kataoka K, Shiraishi Y, Takeda Y, Sakata S, Matsumoto M, Nagano S, Maeda T, Nagata Y, Kitanaka A, Mizuno S, Tanaka H, Chiba K, Ito S, Watatani Y, Kakiuchi N, Suzuki H, Yoshizato T, Yoshida K, Sanada M, Itonaga H, Imaizumi Y, Totoki Y, Munakata W, Nakamura H, Hama N, Shide K, Kubuki Y, Hidaka T, Kameda T, Masuda K, Minato N, Kashiwase K, Izutsu K, Takaori-Kondo A, Miyazaki Y, Takahashi S, Shibata T, Kawamoto H, Akatsuka Y, Shimoda K, Takeuchi K, Seya T, Miyano S, Ogawa S. Nature.534(7607):402-406,2016.
|
| Frequent pathway mutations of splicing machinery in myelodysplasia. Yoshida K, Sanada M, Shiraishi Y, Nowak D, Nagata Y, Yamamoto R, Sato Y, Sato-Otsubo A, Kon A, Nagasaki M, Chalkidis G, Suzuki Y, Shiosaka M, Kawahata R, Yamaguchi T, Otsu M, Obara N, Sakata-Yanagimoto M, Ishiyama K, Mori H, Nolte F, Hofmann WK, Miyawaki S, Sugano S, Haferlach C, Koeffler HP, Shih LY, Haferlach T, Chiba S, Nakauchi H, Miyano S, Ogawa S. Nature. 478(7367):64-69, 2011.
|
|
