Mitsuhashi Satomi

ミツハシサトミ | Mitsuhashi Satomi

Affiliation and department：
Other affiliations (1)：

St.Marianna University School of Medicine Division of Neurology, Department of Internal Medicine

Homepage URL (1)： http://kaken.nii.ac.jp/d/r/40466222.ja.html

Research field (5)： Neurology , Medical biochemistry , Molecular biology , Genomics , Fetal medicine/Pediatrics

Research keywords (5)：遺伝学 , 神経内科学 , リン脂質 , 筋病学 , ミトコンドリア

Research theme for competitive and other funds (7)：

2021 - 2024 DUX4による非コードDNAの転写活性化の病理的意義の研究
2019 - 2022 Analysis of neurological genetic diseases using nanopore long read sequencer
2018 - 2021 Search for endogenous retroviruses involved in FSHD
2017 - 2020 Identification and function of endogenous retrovirus derived genes that mediate cell fusion
2017 - 2019 Roles of MEGF10 in the pathomechanisms of myopathy

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Papers (169)：

Sachiko Ohori, Hironao Numabe, Satomi Mitsuhashi, Naomi Tsuchida, Yuri Uchiyama, Eriko Koshimizu, Kohei Hamanaka, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, et al. Complex chromosomal 6q rearrangements revealed by combined long-molecule genomics technologies. Genomics. 2024. 110894-110894
Keiji Tachikawa, Takahiro Shimizu, Takeshi Imai, Riyoko Ko, Yosuke Kawai, Yosuke Omae, Katsushi Tokunaga, Martin C Frith, Yoshihisa Yamano, Satomi Mitsuhashi. Cost-Effective Cas9-Mediated Targeted Sequencing of Spinocerebellar Ataxia Repeat Expansions. The Journal of molecular diagnostics : JMD. 2024. 26. 2. 85-95
Sachiko Ohori, Akihiko Miyauchi, Hitoshi Osaka, Charles Marques Lourenco, Naohiro Arakaki, Toru Sengoku, Kazuhiro Ogata, Rachel Sayuri Honjo, Chong Ae Kim, Satomi Mitsuhashi, et al. Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy. Life science alliance. 2023. 6. 8. e202302025-e202302025
久我亜沙美, 荻原眞帆, 井本清美, 吉岡耕平, 小澤南, 杉下陽堂, 鈴木由妃, 本吉愛, 三橋里美, 右田王介, et al. 乳児の熱性けいれんから家族性が判明した海綿状血管腫. 日本遺伝カウンセリング学会誌. 2023. 44. 2. 165-165
Shiena Watanabe, Ming Lei, Eiji Nakagawa, Eri Takeshita, Kei-Ichiro Inamori, Fumi Shishido, Masayuki Sasaki, Satomi Mitsuhashi, Naomichi Matsumoto, Yuiko Kimura, et al. Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants. Brain & development. 2023. 45. 5. 270-277

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MISC (59)：

上田真保子, 小野悠介, 隅山健太, 三橋里美, 三橋弘明, 中川草. 筋細胞の融合にかかわる内在性レトロウイルス由来の新規遺伝子. 日本進化学会大会プログラム・講演要旨集(Web). 2022. 24th
Jun Sone, Satomi Mitsuhashi, Atsushi Fujita, Hiroshi Takashima, Hiroshi Sugiyama, Yoshihisa Takiyama, Kengo Maeda, Fumiaki Tanaka, Yasushi Iwasaki, Mari Yoshida, et al. Long-read Sequencing Identifies GGC Repeat Expansions in NOTCH2NLC as the Cause of Neuronal Intranuclear Inclusion Disease. NEUROLOGY. 2020. 94. 15
上田真保子, KRYUKOV Kirill, 三橋里美, 三橋弘明, 今西規, 中川草. Genome-wide comparative analysis of endogenous retroviruses that code for proteins in mammalian genomes. 日本分子生物学会年会プログラム・要旨集(Web). 2020. 43rd
上田真保子, KLYUKOV Kirill, 三橋里美, 三橋弘明, 中川草. Evolution and function of retrotransposon derived genes in mammalian genome. 日本進化学会大会プログラム・講演要旨集(Web). 2020. 22nd
上田真保子, KRYUKOV Kirill, 三橋里美, 三橋弘明, 今西規, 中川草. 哺乳類ゲノムに存在するウイルス様タンパク質ドメインをコードする配列のダイナミックな進化. 日本進化学会大会プログラム・講演要旨集(Web). 2019. 21st

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Work history (12)：

2022/06 - 現在 Tokyo Medical and Dental University Medical Research Institute
2022/06 - 現在 St.Marianna University School of Medicine Division of Neurology, Department of Internal Medicine
2020/04 - 2022/05 Medical Research Institute, Tokyo Medical and Dental University Department of Genomic Function and Diversity
2017/04 - 2020/03 横浜市立大学大学院医学研究科助教
2016 - 2017 東海大学医学部基礎医学系分子生命科学特定研究員

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