Author
M. Nakao
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Biology Disciplines
Click to filter author papersSignature Assays, Organisms & Methods
Click to filter · or open tagActivity by Year
2017-2023 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 10 mutual co-author links5 papers
Recent·Most cited
ROR1 plays a critical role in pancreatic tumor-initiating cells with a partial EMT signature.
M. Yamazaki, S. Hino, S. Usuki, Y. Miyazaki, T. Oda, M. Nakao, T. Ito, K. Yamagata
This study identifies ROR1 as a critical marker for pancreatic tumor-initiating cells with a partial EMT signature, showing its role in promoting tumor growth and relapse.
The EMBO Journal · Apr 25, 2023Peer-reviewedCancer Biology
Phosphorylation of phase-separated p62 bodies by ULK1 activates a redox-independent stress response
M. Komatsu, R. Ikeda, D. Noshiro, H. Morishita, S. Takada, S. Kageyama, Y. Fujioka, T. Funakoshi, S. Komatsu-Hirota, R. Arai, E. Ryzhii, M. Abe, T. Koga, M. Nakao, K. Sakimura, , N. N. Noda
This study identifies ULK1 as the kinase responsible for phosphorylating p62, which activates NRF2 in a redox-independent manner through retention of KEAP1 in p62 bodies.
bioRxiv · Dec 21, 2022Cell Biology
LSD1 acts as an epigenetic barrier against glucocorticoid-induced atrophy and exercise-induced hypertrophy in skeletal muscle
H. Araki, S. Hino, K. Anan, K. Kuribayashi, K. Etoh, D. Seko, R. Takase, K. Kohrogi, Y. Hino, Y. Ono, E. Araki, M. Nakao
This study shows LSD1 regulates fiber type-specific responses to stress in skeletal muscle by modulating gene expression through epigenetic mechanisms.
bioRxiv · Oct 8, 2022Cell Biology
Ki-67 and condensins support the integrity of mitotic chromosomes through distinct mechanisms
M. Takagi, T. Ono, T. Natsume, C. Sakamoto, M. Nakao, N. Saitoh, M. T. Kanemaki, T. Hirano, N. Imamoto
This study shows Ki-67 and condensins have independent yet cooperative roles in maintaining mitotic chromosome structure through distinct mechanisms.
bioRxiv · Oct 12, 2017Cell Biology