1. Characterization of genetic‐origin‐dependent monoallelic expression in mouse embryonic stem cells. (11th December 2019) Authors: Ohishi, Hiroaki; Au Yeung, Wan Kin; Unoki, Motoko; Ichiyanagi, Kenji; Fukuda, Kei; Maenohara, Shoji; Shirane, Kenjiro; Chiba, Hatsune; Sado, Takashi; Sasaki, Hiroyuki Journal: Genes to cells Issue: Volume 25:Number 1(2020) Page Start: 54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromatin remodeling in replication‐uncoupled maintenance DNA methylation and chromosome stability: Insights from ICF syndrome studies. (7th May 2021) Authors: Unoki, Motoko Journal: Genes to cells Issue: Volume 26:Number 6(2021) Page Start: 349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia. Issue 2 (26th February 2021) Authors: Morikawa, Takuya; Ohishi, Hiroaki; Kosaka, Kengo; Shimojo, Tomofumi; Nagano, Akihiro; Taniguchi, Itsuki; Fujioka, Ryuta; Moriyama, Kosei; Unoki, Motoko; Takahashi, Masatomo; Nakao, Motonao; Izumi, Yoshihiro; Bamba, Takeshi; Sasaki, Hiroyuki; Miura, Shiroh; Shibata, Hiroki Journal: Bioscience reports Issue: Volume 41:Issue 2(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Identification of SLC38A7 as a Prognostic Marker and Potential Therapeutic Target of Lung Squamous Cell Carcinoma. Issue 3 (September 2021) Authors: Haratake, Naoki; Hu, Qingjiang; Okamoto, Tatsuro; Jogo, Tomoko; Toyokawa, Gouji; Kinoshita, Fumihiko; Takenaka, Tomoyoshi; Tagawa, Tetsuzo; Iseda, Norifumi; Itoh, Shinji; Yamada, Yuichi; Oda, Yoshinao; Shimokawa, Mototsugu; Kikutake, Chie; Suyama, Mikita; Unoki, Motoko; Sasaki, Hiroyuki; Mori, Ma... Journal: Annals of surgery Issue: Volume 274:Issue 3(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of ZBTB24 protein domains and motifs for heterochromatin localization and transcriptional activation. (15th October 2019) Authors: Aktar, Sharmin; Sasaki, Hiroyuki; Unoki, Motoko Journal: Genes to cells Issue: Volume 24:Number 11(2019) Page Start: 746 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation. Issue 9 (2nd December 2022) Authors: Unoki, Motoko; Velasco, Guillaume; Kori, Satomi; Arita, Kyohei; Daigaku, Yasukazu; Yeung, Wan Kin Au; Fujimoto, Akihiro; Ohashi, Hirofumi; Kubota, Takeo; Miyake, Kunio; Sasaki, Hiroyuki Journal: Human molecular genetics Issue: Volume 32:Issue 9(2023) Page Start: 1439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Serine 298 Phosphorylation in Linker 2 of UHRF1 Regulates Ligand-Binding Property of Its Tandem Tudor Domain. Issue 14 (26th June 2020) Authors: Kori, Satomi; Jimenji, Tomohiro; Ekimoto, Toru; Sato, Miwa; Kusano, Fumie; Oda, Takashi; Unoki, Motoko; Ikeguchi, Mitsunori; Arita, Kyohei Journal: Journal of molecular biology Issue: Volume 432:Issue 14(2020) Page Start: 4061 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗