Rchr
J-GLOBAL ID：201401088746698154
Update date: Jan. 30, 2024
Nakamura Sachie
ナカムラ サチエ | Nakamura Sachie
Affiliation and department：
Homepage URL (1)：
http://kaken.nii.ac.jp/d/r/20382955.ja.html
Research field (1)：
Fetal medicine/Pediatrics
Research keywords (3)：
AAV
, glucose transporter-1 deficiency syndrome
, GLUT1
Research theme for competitive and other funds (4)：
- 2019 - 2023 The establishment of early diagnostic method for glucose transporter-1 deficiency syndrome
- 2017 - 2019 Gene therapy for a mouse model of glucose transporter-1 deficiency syndrome using AAV vector
- 2010 - 2012 Elucidation of the pathogenesis of Langerhans cell histiocytosis from the point of bone immunology
- 2008 - 2010 The role of endothelial progenitor cells and VEGF,VEGF-C in proliferating infantile hemangioma.
Papers (11)：
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Sachie Nakamura, Yasushi Ito, Hiroko Hayakawa, Shiho Aoki, Takanori Yamagata, Hitoshi Osaka. Establishment of a flow cytometry screening method for patients with glucose transporter 1 deficiency syndrome. Molecular genetics and metabolism reports. 2023. 34. 100954-100954
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Shinichi Kumagai, Takeshi Nakajima, Kuniko Shimazaki, Takeharu Kakiuchi, Norihiro Harada, Hiroyuki Ohba, Yoshiyuki Onuki, Naomi Takino, Mika Ito, Makoto Sato, et al. Early distribution of18 F-labeled AAV9 vectors in the cerebrospinal fluid after intracerebroventricular or intracisternal magna infusion in non-human primates. The journal of gene medicine. 2023. 25. 1. e3457
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Sachie Nakamura, Hitoshi Osaka, Shin-Ichi Muramatsu, Naomi Takino, Mika Ito, Eriko F Jimbo, Chika Watanabe, Shuji Hishikawa, Takeshi Nakajima, Takanori Yamagata. Intra-cisterna magna delivery of an AAV vector with the GLUT1 promoter in a pig recapitulates the physiological expression of SLC2A1. Gene therapy. 2021. 28. 6. 329-338
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Yoshie Kurokawa, Hitoshi Osaka, Takeshi Kouga, Eriko Jimbo, Kazuhiro Muramatsu, Sachie Nakamura, Yuki Takayanagi, Tatsushi Onaka, Shin-Ichi Muramatsu, Takanori Yamagata. Gene Therapy in a Mouse Model of Niemann-Pick Disease Type C1. Human gene therapy. 2021. 32. 11-12. 589-598
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Sachie Nakamura, Shin-Ichi Muramatsu, Naomi Takino, Mika Ito, Eriko F Jimbo, Kuniko Shimazaki, Tatsushi Onaka, Sumio Ohtsuki, Tetsuya Terasaki, Takanori Yamagata, et al. Gene therapy for Glut1-deficient mouse using an adeno-associated virus vector with the human intrinsic GLUT1 promoter. The journal of gene medicine. 2018. 20. 4. e3013
ｍore...
MISC (3)：
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Akira Morimoto, Yukiko Oh, Sachie Nakamura, Yoko Shioda, Tomomi Hayase, Toshihiko Imamura, Kazuko Kudo, Shinsaku Imashuku. Inflammatory serum cytokines and chemokines increase associated with the disease extent in pediatric Langerhans cell histiocytosis. CYTOKINE. 2017. 97. 73-79
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Sachie Nakamura, Hitoshi Osaka, Shin-ichi Muramatsu, Naomi Takino, Mika Ito, Shiho Aoki, Eriko F. Jimbo, Kuniko Shimazaki, Tatsushi Onaka, Sumio Ohtsuki, et al. Gene Therapy for a Mouse Model of Glucose Transporter-1 Deficiency Syndrome. MOLECULAR THERAPY. 2017. 25. 5. 108-108
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門田 行史, 中瀬 葉子, 中村 幸恵, 早瀬 朋美, 翁 由紀子, 柏井 良文, 郡司 勇治, 今村 俊彦, 森本 哲, 桃井 真里子. 眼球突出で発症したB前駆型急性リンパ性白血病/非ホジキンリンパ腫の2例. 小児科臨床. 2011. 64. 9. 2047-2051
Work history (4)：
- 2020/04 - 現在 Jichi Medical University Department of Pediatrics, School of Medicine Assistant Professor
- 2017/04 - 2018/03 Jichi Medical University Department of Pediatrics, School of Medicine
- 2012/04 - 2013/03 Jichi Medical University Department of Pediatrics, School of Medicine
- 2008 - 2011 Jichi Medical University Department of Pediatrics, School of Medicine
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