A Posttranslationally Regulated Protease, VheA, Is Involved in the Liberation of Juveniles from Parental Spheroids in Volvox carteri

Por Fukada, Kazutake, Inoue, Tan, Shiraishi, Hideaki
Publicado em 2006

Structure–function relationships of two closely related group IC3 intron ribozymes from Azoarcus and Synechococcus pre-tRNA

Por Ikawa, Yoshiya, Naito, Daisuke, Shiraishi, Hideaki, Inoue, Tan
Publicado em 2000

Design and development of a catalytic ribonucleoprotein

Por Atsumi, Shota, Ikawa, Yoshiya, Shiraishi, Hideaki, Inoue, Tan
Publicado em 2001

Selections for constituting new RNA–protein interactions in catalytic RNP

Por Atsumi, Shota, Ikawa, Yoshiya, Shiraishi, Hideaki, Inoue, Tan
Publicado em 2003

Modular engineering of a Group I intron ribozyme

Por Ohuchi, Shoji J., Ikawa, Yoshiya, Shiraishi, Hideaki, Inoue, Tan
Publicado em 2002

Generation of a catalytic module on a self-folding RNA

Por YOSHIOKA, WATARU, IKAWA, YOSHIYA, JAEGER, LUC, SHIRAISHI, HIDEAKI, INOUE, TAN
Publicado em 2004

Generation of a catalytic module on a self-folding RNA

Por YOSHIOKA, WATARU, IKAWA, YOSHIYA, JAEGER, LUC, SHIRAISHI, HIDEAKI, INOUE, TAN
Publicado em 2005

Akinetopsia as epileptic seizure()

Por Sakurai, Kotaro, Kurita, Tsugiko, Takeda, Youji, Shiraishi, Hideaki, Kusumi, Ichiro
Publicado em 2013

PM341. Magnetoenceaphalography as a potential candidate to detect treatment effect of dyslexia

Por Yagyu, Kazuyori, Saitoh, Takuya, Shimojo, Atsushi, Shiraishi, Hideaki, Suyuma, Satoshi
Publicado no Int J Neuropsychopharmacol (2016)

Efficacy of perampanel for controlling seizures and improving neurological dysfunction in a patient with dentatorubral-pallidoluysian atrophy (DRPLA)

Por Shiraishi, Hideaki, Egawa, Kiyoshi, Ito, Tomoshiro, Kawano, Osamu, Asahina, Naoko, Kohsaka, Shinobu
Publicado no Epilepsy Behav Case Rep (2017)

The Involvement of Sensory-motor Networks in Reflex Seizure

Por Suzuki, Hime, Enatsu, Rei, Kanno, Aya, Ochi, Satoko, Murahara, Takashi, Yazawa, Shogo, Shiraishi, Hideaki, Mikuni, Nobuhiro
Publicado no NMC Case Rep J (2017)

A Longer Polyalanine Expansion Mutation in the ARX Gene Causes Early Infantile Epileptic Encephalopathy with Suppression-Burst Pattern (Ohtahara Syndrome)

Por Kato, Mitsuhiro , Saitoh, Shinji , Kamei, Atsushi , Shiraishi, Hideaki , Ueda, Yuki , Akasaka, Manami , Tohyama, Jun , Akasaka, Noriyuki , Hayasaka, Kiyoshi 
Publicado em 2007

Efficacy of adjuvant chemotherapy for non-small cell lung cancer assessed by metastatic potential associated with ACTN4

Por Miura, Nami, Kamita, Masahiro, Kakuya, Takanori, Fujiwara, Yutaka, Tsuta, Koji, Shiraishi, Hideaki, Takeshita, Fumitaka, Ochiya, Takahiro, Shoji, Hirokazu, Huang, Wilber, Ohe, Yuichiro, Yamada, Tesshi, Honda, Kazufumi
Publicado no Oncotarget (2016)

Comparison of Three Methods for Localizing Interictal Epileptiform Discharges with Magnetoencephalography

Por Shiraishi, Hideaki, Ahlfors, Seppo P., Stufflebeam, Steven M., Knake, Susanne, Larsson, Pål G., Hämäläinen, Matti S., Takano, Kyoko, Okajima, Maki, Hatanaka, Keisaku, Saitoh, Shinji, Dale, Anders M., Halgren, Eric
Publicado em 2011

Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay

Por Saitsu, Hirotomo, Watanabe, Miho, Akita, Tenpei, Ohba, Chihiro, Sugai, Kenji, Ong, Winnie Peitee, Shiraishi, Hideaki, Yuasa, Shota, Matsumoto, Hiroshi, Beng, Khoo Teik, Saitoh, Shinji, Miyatake, Satoko, Nakashima, Mitsuko, Miyake, Noriko, Kato, Mitsuhiro, Fukuda, Atsuo, Matsumoto, Naomichi
Publicado no Sci Rep (2016)

Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan

Por Yamada, Kenji, Shiraishi, Hideaki, Oki, Eishin, Ishige, Mika, Fukao, Toshiyuki, Hamada, Yusuke, Sakai, Norio, Ochi, Fumihiro, Watanabe, Asami, Kawakami, Sanae, Kuzume, Kazuyo, Watanabe, Kenji, Sameshima, Koji, Nakamagoe, Kiyotaka, Tamaoka, Akira, Asahina, Naoko, Yokoshiki, Saki, Miyakoshi, Takashi, Ono, Kota, Oba, Koji, Isoe, Toshiyuki, Hayashi, Hiroshi, Yamaguchi, Seiji, Sato, Norihiro
Publicado no Mol Genet Metab Rep (2018)

Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

Por Hori, Ikumi, Otomo, Takanobu, Nakashima, Mitsuko, Miya, Fuyuki, Negishi, Yutaka, Shiraishi, Hideaki, Nonoda, Yutaka, Magara, Shinichi, Tohyama, Jun, Okamoto, Nobuhiko, Kumagai, Takeshi, Shimoda, Konomi, Yukitake, Yoshiya, Kajikawa, Daigo, Morio, Tomohiro, Hattori, Ayako, Nakagawa, Motoo, Ando, Naoki, Nishino, Ichizo, Kato, Mitsuhiro, Tsunoda, Tatsuhiko, Saitsu, Hirotomo, Kanemura, Yonehiro, Yamasaki, Mami, Kosaki, Kenjiro, Matsumoto, Naomichi, Yoshimori, Tamotsu, Saitoh, Shinji
Publicado no Sci Rep (2017)