Author

A. Kuma

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Assay:bulk RNA-seq· 2 Research Focus:cell signaling & trafficking· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

H. Kosako· 2 shared T. Kaminishi· 2 shared T. Shima· 2 shared T. Yoshimori· 2 shared A. Takahashi· 1 shared H. Omori· 1 shared I. Shimomura· 1 shared K. Nishino· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersCell Biology

H. Kosako

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

The Rubicon-WIPI axis regulates exosome biogenesis during aging

K. Yanagawa, A. Kuma, M. Hamasaki, S. Kita, T. Yamamuro, K. Nishino, S. Nakamura, H. Omori, T. Kaminishi, S. Oikawa, Y. Kato, R. Edahiro, R. Kawagoe, T. Taniguchi, Y. Tanaka, , T. Yoshimori

This study identifies the Rubicon-WIPI axis as a regulator of exosome biogenesis, showing its role in age-dependent exosome release and microRNA fate in mice.

bioRxiv · May 8, 2024 · PreprintCell Biology

Golgi membrane proteins YIPF3 and YIPF4 regulate turnover of the Golgi apparatus through autophagy

S. Kitta, T. Kaminishi, M. Higashi, T. Shima, H. Kosako, T. Yoshimori, A. Kuma

This study identifies YIPF3 and YIPF4 as Golgi-specific autophagy receptors that mediate Golgi turnover via selective autophagy.

bioRxiv · Aug 9, 2023 · PreprintCell Biology

Autophagy controls lipid droplet formation by fine-tuning NCoR1 levels

M. Komatsu, Y.-S. Sou, M. Koike, N. Mizushima, S. Waguri, S. Terai, A. Kuma, T. Saito, S.-s. Takahashi, T. Yabe

This study shows autophagy regulates lipid droplet formation by modulating NCoR1 levels, affecting LXR target gene expression and lipid metabolism in the liver.

bioRxiv · Aug 1, 2019 · PreprintCell Biology