1. Established Stem Cell Model of Spinal Muscular Atrophy Is Applicable in the Evaluation of the Efficacy of Thyrotropin‐Releasing Hormone Analog. (18th December 2015) Authors: Ohuchi, Kazuki; Funato, Michinori; Kato, Zenichiro; Seki, Junko; Kawase, Chizuru; Tamai, Yuya; Ono, Yoko; Nagahara, Yuki; Noda, Yasuhiro; Kameyama, Tsubasa; Ando, Shiori; Tsuruma, Kazuhiro; Shimazawa, Masamitsu; Hara, Hideaki; Kaneko, Hideo Journal: Stem cells translational medicine Issue: Volume 5:Number 2(2016) Page Start: 152 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. VGF nerve growth factor inducible is involved in retinal ganglion cells death induced by optic nerve crush. Issue 1 (December 2018) Authors: Takeuchi, Hiroto; Inagaki, Satoshi; Morozumi, Wataru; Nakano, Yukimichi; Inoue, Yuki; Kuse, Yoshiki; Mizoguchi, Takahiro; Nakamura, Shinsuke; Funato, Michinori; Kaneko, Hideo; Hara, Hideaki; Shimazawa, Masamitsu Journal: Scientific reports Issue: Volume 8:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Early phase 2 trial of TAS‐205 in patients with Duchenne muscular dystrophy. Issue 2 (20th January 2020) Authors: Komaki, Hirofumi; Maegaki, Yoshihiro; Matsumura, Tsuyoshi; Shiraishi, Kazuhiro; Awano, Hiroyuki; Nakamura, Akinori; Kinoshita, Satoru; Ogata, Katsuhisa; Ishigaki, Keiko; Saitoh, Shinji; Funato, Michinori; Kuru, Satoshi; Nakayama, Takahiro; Iwata, Yasuyuki; Yajima, Hiroyuki; Takeda, Shin'ichi Journal: Annals of clinical and translational neurology Issue: Volume 7:Issue 2(2020) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Noonan syndrome‐like phenotype in a patient with heterozygous ERF truncating variant. (11th July 2021) Authors: Yamada, Mamiko; Funato, Michinori; Kondo, Goro; Suzuki, Hisato; Uehara, Tomoko; Takenouchi, Toshiki; Sakamoto, Yoshiaki; Kosaki, Kenjiro Journal: Congenital anomalies Issue: Volume 61:Number 6(2021) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Impairment of oligodendrocyte lineages in spinal muscular atrophy model systems. Issue 5 (20th March 2019) Authors: Ohuchi, Kazuki; Funato, Michinori; Ando, Shiori; Inagaki, Satoshi; Sato, Arisu; Kawase, Chizuru; Seki, Junko; Nakamura, Shinsuke; Shimazawa, Masamitsu; Kaneko, Hideo; Hara, Hideaki Journal: NeuroReport Issue: Volume 30:Issue 5(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cohesinopathy presenting with microtia, facial palsy, and hearing loss caused by STAG1 pathogenic variant. (30th December 2021) Authors: Funato, Michinori; Uehara, Tomoko; Okada, Yuki; Kaneko, Hideo; Kosaki, Kenjiro Journal: Congenital anomalies Issue: Volume 62:Number 2(2022) Page Start: 82 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Established Stem Cell Model of Spinal Muscular Atrophy Is Applicable in the Evaluation of the Efficacy of Thyrotropin-Releasing Hormone Analog. (18th December 2015) Authors: Ohuchi, Kazuki; Funato, Michinori; Kato, Zenichiro; Seki, Junko; Kawase, Chizuru; Tamai, Yuya; Ono, Yoko; Nagahara, Yuki; Noda, Yasuhiro; Kameyama, Tsubasa; Ando, Shiori; Tsuruma, Kazuhiro; Shimazawa, Masamitsu; Hara, Hideaki; Kaneko, Hideo Journal: Stem cells translational medicine Issue: Volume 5:Number 2(2016) Page Start: 152 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Characteristics of Li‐Fraumeni syndrome in Japan: A review study by the special committee of JSHT. Issue 7 (17th May 2021) Authors: Funato, Michinori; Tsunematsu, Yukiko; Yamazaki, Fumito; Tamura, Chieko; Kumamoto, Tadashi; Takagi, Masatoshi; Kato, Shunsuke; Sugimura, Haruhiko; Tamura, Kazuo Other Names: investigator. Journal: Cancer science Issue: Volume 112:Issue 7(2021) Page Start: 2821 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study. Issue 12 (7th December 2020) Authors: Komaki, Hirofumi; Takeshima, Yasuhiro; Matsumura, Tsuyoshi; Ozasa, Shiro; Funato, Michinori; Takeshita, Eri; Iwata, Yasuyuki; Yajima, Hiroyuki; Egawa, Yoichi; Toramoto, Takuya; Tajima, Masaya; Takeda, Shinichi Journal: Annals of clinical and translational neurology Issue: Volume 7:Issue 12(2020) Page Start: 2393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Three patients with DeSanto‐Shinawi syndrome: Further phenotypic delineation. Issue 6 (16th April 2018) Authors: Uehara, Tomoko; Ishige, Takashi; Hattori, Shigeto; Yoshihashi, Hiroshi; Funato, Michinori; Yamaguchi, Yu; Takenouchi, Toshiki; Kosaki, Kenjiro Journal: American journal of medical genetics Issue: Volume 176:Issue 6(2018) Page Start: 1335 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗