2012 - 2015 A role of UHRF1 in establishment and maintenance of genomic imprinting
2012 - 2012 ヒストンのリジン残基 「水酸化」の生理的意義の解明
2011 - 2012 Identification of novel methyl-DNA binding proteins
2010 - 2011 Clarification of roles of UHRF1 in "Epigenetic regulation of transcription", "Transfer of histon modifications", and "Imprinting"
2010 - 2011 Analysis of a novel histone modification associated with the UHRF1 complex
2004 - 2005 癌抑制遺伝子p53の下流遺伝子 の同定と機能解析
2001 - 2002 癌抑制遺伝子PTENの下流遺伝子の単離と機能解析
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Papers (51):
Masatomo So, Misaki Ono, Shigeki Oogai, Minako Kondo, Kaede Yamazaki, Charlotte Nachtegael, Hiroshi Hamajima, Risa Mutoh, Masaki Kato, Hisaya Kawate, et al. Inhibitory effects of extracts from Eucalyptus gunnii on α-synuclein amyloid fibrils. Bioscience, Biotechnology, and Biochemistry. 2024
Motoko Unoki, Shuhei Uemura, Akihiro Fujimoto, Hiroyuki Sasaki. The maternal protein NLRP5 stabilizes UHRF1 in the cytoplasm: implication for the pathogenesis of multilocus imprinting disturbance. Human Molecular Genetics. 2024. 33. 18. 1575-1583
Unoki, M. Exploring the intersection of epigenetics, DNA repair, and immunology from studies of ICF syndrome, an inborn error of immunity. Frontiers in Immunology. 2024. 15. 1405022
Kugui Yoshida-Tanaka, Ko Ikemoto, Ryoji Kuribayashi, Motoko Unoki, Takako Takano, Akihiro Fujimoto. Long-read sequencing reveals the complex structure of extra dic(21;21) chromosome and its biological effects. Human Genetics. 2023. 142. 9. 1375-1384
Shuhei Uemura, Shoji Maenohara, Kimiko Inoue, Narumi Ogonuki, Shogo Matoba, Atsuo Ogura, Mayuko Kurumizaka, Kazuo Yamagata, Jafar Sharif, Haruhiko Koseki, et al. UHRF1 is essential for proper cytoplasmic architecture and function of mouse oocytes and derived embryos. Life Science Alliance. 2023. 6. 8. e202301904-e202301904
Congenital diseases with defects in maintenance DNA methylation: ICF syndrome and multi-locus imprinting disturbance
(The 1st CDCA7 mini-symposium 2024)
Exploration of Cancer Driver Genes Using Three Dimensional Protein Structures
(The 69th Annual Meeting of the Japan Society of Human Genetics 2024)
Transcriptome analysis of adult T-cell leukemia using long-read sequencing technology
(The 69th Annual Meeting of the Japan Society of Human Genetics 2024)
Elucidation of the molecular pathogenesis of congenital diseases with DNA methylation abnormalities
(The Genetics Society of Japan 96th Annual Meeting 2024)
Transcriptome analysis of adult T-cell leukemia using long-read sequencing technology
(2024)
2015/09 - 内藤記念科学振興財団 The 40th Naito Conference Best poster award
2013/08 - 第25回高遠シンポジウム優秀ポスター賞
1999/03 - 日本獣医師会 日本獣医師会賞
1994/03 - 竹岸・越智賞
Association Membership(s) (6):
The Genetics Society of Japan
, The Japan Society of Human Genetics
, The molecular biology society of Japan
, The Japanese Society for Epigenetics
, American Association for Cancer Research
, Japanese Cancer Association