11. Expression profile analysis in cells overexpressing DRPLA cDNA to explore the roles of DRPLAp as a transcriptional coregulator. Issue 4 (11th May 2022) Authors: Hatano, Keiko; Date, Hidetoshi; Ishiura, Hiroyuki; Matsukawa, Takashi; Tanaka, Masaki; Mitsui, Jun; Goto, Jun; Yoshimura, Jun; Doi, Koichiro; Morishita, Shinichi; Tsuji, Shoji Journal: Neurology and clinical neuroscience Issue: Volume 10:Issue 4(2022) Page Start: 210 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation. Issue 5 (15th February 2021) Authors: Ishino, Kyoko; Hasuwa, Hidetoshi; Yoshimura, Jun; Iwasaki, Yuka W; Nishihara, Hidenori; Seki, Naomi M; Hirano, Takamasa; Tsuchiya, Marie; Ishizaki, Hinako; Masuda, Harumi; Kuramoto, Tae; Saito, Kuniaki; Sakakibara, Yasubumi; Toyoda, Atsushi; Itoh, Takehiko; Siomi, Mikiko C; Morishita, Shinichi; S... Journal: Nucleic acids research Issue: Volume 49:Issue 5(2021) Page Start: 2700 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing. Issue 7 (13th June 2017) Authors: Eriguchi, Yosuke; Kuwabara, Hitoshi; Inai, Aya; Kawakubo, Yuki; Nishimura, Fumichika; Kakiuchi, Chihiro; Tochigi, Mamoru; Ohashi, Jun; Aoki, Naoto; Kato, Kayoko; Ishiura, Hiroyuki; Mitsui, Jun; Tsuji, Shoji; Doi, Koichiro; Yoshimura, Jun; Morishita, Shinichi; Shimada, Takafumi; Furukawa, Masaomi;... Journal: American journal of medical genetics Issue: Volume 174:Issue 7(2017) Page Start: 712 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. 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) ↗
15. Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis. Issue 3 (11th February 2022) Authors: Ikenaga, Chiseko; Date, Hidetoshi; Kanagawa, Motoi; Mitsui, Jun; Ishiura, Hiroyuki; Yoshimura, Jun; Pinal‐Fernandez, Iago; Mammen, Andrew L.; Lloyd, Thomas E.; Tsuji, Shoji; Shimizu, Jun; Toda, Tatsushi; Goto, Jun Journal: Annals of neurology Issue: Volume 91:Issue 3(2022) Page Start: 317 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. 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) ↗
17. Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. (April 2019) Authors: Ichinose, Yuta; Ishiura, Hiroyuki; Tanaka, Masaki; Yoshimura, Jun; Doi, Koichiro; Umeda, Takako; Yamauchi, Hajime; Tsuchiya, Mai; Koh, Kishin; Yamashiro, Nobuo; Mitsui, Jun; Goto, Jun; Onishi, Hiroshi; Ohtsuka, Toshihisa; Shindo, Kazumasa; Morishita, Shinichi; Tsuji, Shoji; Takiyama, Yoshihisa Journal: Parkinsonism & related disorders Issue: Volume 61(2019) Page Start: 57 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. 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) ↗
19. Novel mutation in the membrane metalloendopeptidase gene in a patient with the autosomal recessive form of Charcot–Marie–Tooth disease. Issue 4 (20th June 2017) Authors: Ishiura, Hiroyuki; Mitsui, Jun; Yoshimura, Jun; Doi, Koichiro; Morishita, Shinichi; Hamada, Masashi; Goto, Jun; Tsuji, Shoji Journal: Neurology and clinical neuroscience Issue: Volume 5:Issue 4(2017:Jul.) Page Start: 124 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Sporadic progressive myoclonic epilepsy with early‐onset dementia caused by a de novo mutation in PSEN1. Issue 5 (4th July 2019) Authors: Taminato, Tomoya; Araki, Manabu; Sato, Noriko; Ishiura, Hiroyuki; Mitsui, Jun; Yoshimura, Jun; Doi, Koichiro; Morishita, Shinichi; Tsuji, Shoji; Takahashi, Yuji Journal: Neurology and clinical neuroscience Issue: Volume 7:Issue 5(2019:Sep.) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗