1. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations. (30th June 2020) Authors: Sakata, Sonoko; Tsumura, Miyuki; Matsubayashi, Tadashi; Karakawa, Shuhei; Kimura, Shunsuke; Tamaura, Moe; Okano, Tsubasa; Naruto, Takuya; Mizoguchi, Yoko; Kagawa, Reiko; Nishimura, Shiho; Imai, Kohsuke; Le Voyer, Tom; Casanova, Jean-Laurent; Bustamante, Jacinta; Morio, Tomohiro; Ohara, Osamu; Kob... Journal: International immunology Issue: Volume 32:Number 10(2020) Page Start: 663 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Discovery of potent α1L-adrenoceptor agonists: Design and synthesis of bicyclic derivatives. Issue 16 (15th August 2015) Authors: Suzuki, Shinya; Okano, Tsubasa; Horiuchi, Rie; Hareyama, Nana; Amikura, Kazutoshi; Yamamoto, Naoyoshi; Yoshizawa, Yoshitaka; Yagi, Mai; Serizawa, Kanako; Hayashi, Ryoji Journal: Bioorganic & medicinal chemistry letters Issue: Volume 25:Issue 16(2015) Page Start: 3368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Discovery of potent α1L-adrenoceptor agonists: Design and synthesis of bicyclic derivatives. Issue 16 (15th August 2015) Authors: Suzuki, Shinya; Okano, Tsubasa; Horiuchi, Rie; Hareyama, Nana; Amikura, Kazutoshi; Yamamoto, Naoyoshi; Yoshizawa, Yoshitaka; Yagi, Mai; Serizawa, Kanako; Hayashi, Ryoji Journal: Bioorganic & medicinal chemistry letters Issue: Volume 25:Issue 16(2015) Page Start: 3368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Dysphagia as a result of ossification of the anterior longitudinal ligament in a patient with myotonic dystrophy. Issue 1 (20th February 2014) Authors: Ishizawa, Keisuke; Okano, Tsubasa; Sasaki, Takahiro; Tomioka, Ryo; Araki, Nobuo Journal: Neurology and clinical neuroscience Issue: Volume 2:Issue 1(2014:Jan.) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation. (19th April 2018) Authors: Hoshino, Akihiro; Takashima, Takehiro; Yoshida, Kenichi; Morimoto, Akira; Kawahara, Yuta; Yeh, Tzu-Wen; Okano, Tsubasa; Yamashita, Motoi; Mitsuiki, Noriko; Imai, Kohsuke; Sakatani, Takashi; Nakazawa, Atsuko; Okuno, Yusuke; Shiraishi, Yuichi; Chiba, Kenichi; Tanaka, Hiroko; Miyano, Satoru; Ogawa, ... Journal: Journal of infectious diseases Issue: Volume 218:Number 5(2018) Page Start: 825 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation. Issue 2 (29th September 2017) Authors: Takagi, Masatoshi; Hoshino, Akihiro; Yoshida, Kenichi; Ueno, Hiroo; Imai, Kohsuke; Piao, Jinhua; Kanegane, Hirokazu; Yamashita, Motoi; Okano, Tsubasa; Muramatsu, Hideki; Okuno, Yusuke; Shiraishi, Yuichi; Chiba, Kenichi; Tanaka, Hiroko; Miyano, Satoru; Ogawa, Seishi; Hayashi, Yasuhide; Kojima, Sei... Journal: Pediatric blood & cancer Issue: Volume 65:Issue 2(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. High‐throughput analysis revealed the unique immunoglobulin gene rearrangements in plasmacytoma‐like post‐transplant lymphoproliferative disorder. (19th March 2020) Authors: Hoshino, Akihiro; Nishimura, Akira; Naruto, Takuya; Okano, Tsubasa; Matsumoto, Kazuaki; Okamoto, Keisuke; Shintaku, Hiroshi; Tokoro, Shown; Okamoto, Hiroyuki; Wada, Taizo; Takagi, Masatoshi; Imai, Kohsuke; Kanegane, Hirokazu; Morio, Tomohiro Journal: British journal of haematology Issue: Volume 189:Number 4(2020) Page Start: e164 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Novel compound heterozygous mutations in a Japanese girl with Janus kinase 3 deficiency. Issue 10 (4th September 2016) Authors: Sato, Takeshi; Okano, Tsubasa; Tanaka‐Kubota, Mari; Kimura, Shunsuke; Miyamoto, Satoshi; Ono, Shintaro; Yamashita, Motoi; Mitsuiki, Noriko; Takagi, Masatoshi; Imai, Kohsuke; Kajiwara, Michiko; Ebato, Takasuke; Ogata, Shohei; Oda, Hirotsugu; Ohara, Osamu; Kanegane, Hirokazu; Morio, Tomohiro Journal: Pediatrics international Issue: Volume 58:Issue 10(2016) Page Start: 1076 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prominent dermal Langerhans cells in an Omenn syndrome patient with a novel mutation in the IL2RG gene. Issue 11 (27th August 2019) Authors: Ibusuki, Atsuko; Nishikawa, Takuro; Hiraki, Tsubasa; Okano, Tsubasa; Imai, Kohsuke; Kanegane, Hirokazu; Ohnishi, Hidenori; Kato, Zenichiro; Fujii, Kazuyasu; Tanimoto, Akihide; Kawano, Yoshifumi; Kanekura, Takuro Journal: Journal of dermatology Issue: Volume 46:Issue 11(2019) Page Start: 1019 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations. (16th September 2021) Authors: Okano, Tsubasa; Nishimura, Akira; Inoue, Kento; Naruto, Takuya; Tokoro, Shown; Tomoda, Takahiro; Kamiya, Takahiro; Simbo, Asami; Akutsu, Yuko; Okamoto, Keisuke; Yeh, Tzuwen; Isoda, Takeshi; Yanagimachi, Masakatsu; Kajiwara, Michiko; Imai, Kohsuke; Kanegane, Hirokazu; Mori, Masaaki; Morio, Tomohir... Journal: Rheumatology Issue: Volume 60:Number 12(2021) Page Start: e429 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗