Base editing rescues a hereditary motor neuron disease in mouse and patient-derived iPSC organoid models
- DOI
- 10.1016/j.omta.2026.201835
- Published
- 2026-12
- Container
- Molecular Therapy Advances
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.omta.2026.201835,
title = {Base editing rescues a hereditary motor neuron disease in mouse and patient-derived iPSC organoid models},
author = {Keiko Imamura and Shin Yoshioka and Kota Kamizato and Ryosuke Oki and Hiroyuki Hioki and Kayoko Tsukita and Ikuyo Inoue and Rina Shimizu and Mako Takiguchi and Tomoki Sakasai and Aya Okusa and Ran Shibukawa and Takeshi Niki and Satoko Sakurai and Taro Okunomiya and Takayuki Kondo and Tomohisa Kato and Atsushi Miyanohara and Manabu Kakinohana and Takuya Yamamoto and Martin Marsala and Keiji Nishida and Yuishin Izumi and Haruhisa Inoue},
year = {2026},
journal = {Molecular Therapy Advances},
doi = {10.1016/j.omta.2026.201835},
url = {https://doi.org/10.1016/j.omta.2026.201835}
}RIS
TY - JOUR TI - Base editing rescues a hereditary motor neuron disease in mouse and patient-derived iPSC organoid models AU - Keiko Imamura AU - Shin Yoshioka AU - Kota Kamizato AU - Ryosuke Oki AU - Hiroyuki Hioki AU - Kayoko Tsukita AU - Ikuyo Inoue AU - Rina Shimizu AU - Mako Takiguchi AU - Tomoki Sakasai AU - Aya Okusa AU - Ran Shibukawa AU - Takeshi Niki AU - Satoko Sakurai AU - Taro Okunomiya AU - Takayuki Kondo AU - Tomohisa Kato AU - Atsushi Miyanohara AU - Manabu Kakinohana AU - Takuya Yamamoto AU - Martin Marsala AU - Keiji Nishida AU - Yuishin Izumi AU - Haruhisa Inoue PY - 2026 JO - Molecular Therapy Advances DO - 10.1016/j.omta.2026.201835 UR - https://doi.org/10.1016/j.omta.2026.201835 ER -
APA
Imamura, K., Yoshioka, S., Kamizato, K., Oki, R., Hioki, H., Tsukita, K., Inoue, I., Shimizu, R., Takiguchi, M., Sakasai, T., Okusa, A., Shibukawa, R., Niki, T., Sakurai, S., Okunomiya, T., Kondo, T., Kato, T., Miyanohara, A., Kakinohana, M., Yamamoto, T., Marsala, M., Nishida, K., Izumi, Y., & Inoue, H. (2026). Base editing rescues a hereditary motor neuron disease in mouse and patient-derived iPSC organoid models. Molecular Therapy Advances. https://doi.org/10.1016/j.omta.2026.201835
Source records
- crossref · retrieved 2026-09-25T05:27:30.739Z