AAV-based gene therapy with modified HEXB confers lasting therapeutic benefits in GM2 gangliosidosis models.

Kitakaze K, Ohnishi Y, Tsuji D, Watanabe R, Kamori N, Katakai Y, Shibata H, Yoshizawa S, Ito M, Takino N, Muramatsu SI, Itoh K

Open source

DOI
10.1016/j.xcrm.2026.102762
Published
2026 May 19
Container
Cell reports. Medicine
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.xcrm.2026.102762,
  title = {AAV-based gene therapy with modified HEXB confers lasting therapeutic benefits in GM2 gangliosidosis models.},
  author = {Kitakaze K and Ohnishi Y and Tsuji D and Watanabe R and Kamori N and Katakai Y and Shibata H and Yoshizawa S and Ito M and Takino N and Muramatsu SI and Itoh K},
  year = {2026},
  journal = {Cell reports. Medicine},
  doi = {10.1016/j.xcrm.2026.102762},
  url = {https://doi.org/10.1016/j.xcrm.2026.102762}
}

RIS

TY  - JOUR
TI  - AAV-based gene therapy with modified HEXB confers lasting therapeutic benefits in GM2 gangliosidosis models.
AU  - Kitakaze K
AU  - Ohnishi Y
AU  - Tsuji D
AU  - Watanabe R
AU  - Kamori N
AU  - Katakai Y
AU  - Shibata H
AU  - Yoshizawa S
AU  - Ito M
AU  - Takino N
AU  - Muramatsu SI
AU  - Itoh K
PY  - 2026
JO  - Cell reports. Medicine
DO  - 10.1016/j.xcrm.2026.102762
UR  - https://doi.org/10.1016/j.xcrm.2026.102762
ER  - 

APA

K, K., Y, O., D, T., R, W., N, K., Y, K., H, S., S, Y., M, I., N, T., SI, M., & K, I. (2026). AAV-based gene therapy with modified HEXB confers lasting therapeutic benefits in GM2 gangliosidosis models.. Cell reports. Medicine. https://doi.org/10.1016/j.xcrm.2026.102762

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