1. AgIn: measuring the landscape of CpG methylation of individual repetitive elements. (17th June 2016) Authors: Suzuki, Yuta; Korlach, Jonas; Turner, Stephen W.; Tsukahara, Tatsuya; Taniguchi, Junko; Qu, Wei; Ichikawa, Kazuki; Yoshimura, Jun; Yurino, Hideaki; Takahashi, Yuji; Mitsui, Jun; Ishiura, Hiroyuki; Tsuji, Shoji; Takeda, Hiroyuki; Morishita, Shinichi Journal: Bioinformatics Issue: Volume 32:Number 19(2016) Page Start: 2911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum. (February 2016) Authors: Mano, Kagari Koshi; Matsukawa, Takashi; Mitsui, Jun; Ishiura, Hiroyuki; Tokushige, Shin-ichi; Takahashi, Yuji; Sato, Naoko Saito; Nakamoto, Fumiko Kusunoki; Ichikawa, Yaeko; Nagashima, Yu; Terao, Yasuo; Shimizu, Jun; Hamada, Masashi; Uesaka, Yoshikazu; Oyama, Genko; Ogawa, Go; Yoshimura, Jun; Doi... Journal: Neurology Issue: Volume 2:Number 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines. Issue 1 (December 2016) Authors: Fujimori, Koki; Tezuka, Toshiki; Ishiura, Hiroyuki; Mitsui, Jun; Doi, Koichiro; Yoshimura, Jun; Tada, Hirobumi; Matsumoto, Takuya; Isoda, Miho; Hashimoto, Ryota; Hattori, Nubutaka; Takahashi, Takuya; Morishita, Shinichi; Tsuji, Shoji; Akamatsu, Wado; Okano, Hideyuki Journal: Molecular brain Issue: Volume 9:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mutations in MME cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2. Issue 4 (17th March 2016) Authors: Higuchi, Yujiro; Hashiguchi, Akihiro; Yuan, Junhui; Yoshimura, Akiko; Mitsui, Jun; Ishiura, Hiroyuki; Tanaka, Masaki; Ishihara, Satoshi; Tanabe, Hajime; Nozuma, Satoshi; Okamoto, Yuji; Matsuura, Eiji; Ohkubo, Ryuichi; Inamizu, Saeko; Shiraishi, Wataru; Yamasaki, Ryo; Ohyagi, Yasumasa; Kira, Jun‐i... Journal: Annals of neurology Issue: Volume 79:Issue 4(2016:Apr.) Page Start: 659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel COL6A2 mutation in a case of limb girdle muscular dystrophy phenotype with autosomal recessive inheritance. Issue 5 (13th July 2016) Authors: Mitsui, Jun; Ishiura, Hiroyuki; Yoshimura, Jun; Doi, Koichiro; Morishita, Shinichi; Shoji, Hiroshi; Arimori, Yojiro; Matsumoto, Takafumi; Shimizu, Jun; Tsuji, Shoji Journal: Neurology and clinical neuroscience Issue: Volume 4:Issue 5(2016:Sep.) Page Start: 189 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗