Author

Hideaki Morishita

Kyushu UniversityORCID 0000-0003-0860-8371Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:development & morphogenesis· 2 Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1 Assay:proteomics· 1

Frequent Co-Authors

Manabu AbeiD· 2 shared Elena RyzhiiiD· 1 shared Gaoxin MaoiD· 1 shared Hikaru TsuchiyaiD· 1 shared Kenji SakimuraiD· 1 shared Masaaki KomatsuiD· 1 shared Michitaka SuzukiiD· 1 shared Mitsuyoshi NakaoiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersCell Biology

Manabu AbeORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintMay 21, 2026

High basal autophagic activity in the brain revealed by systemic quantitative analysis using GFP-LC3-RFP mice

Yuki Kanda, Tomoya Eguchi, Hideaki Morishita…·Noboru Mizushima

This study quantifies basal autophagic flux in mice using GFP-LC3-RFP reporter mice, revealing higher flux in brain, liver, and kidney compared to other tissues.

1 citation

mouseexperimental assay

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Cell BiologyEMBO ReportsPeer-reviewedMay 28, 2025

KEAP1 retention in phase-separated p62 bodies drives liver damage in autophagy-deficient conditions

Shuhei Takada, Nozomi Shinomiya, Gaoxin Mao…·Masaaki Komatsu

The paper shows that KEAP1 retention in p62 bodies and NRF2 activation cause liver damage when autophagy is impaired, and that blocking p62-KEAP1 interactions reduces this damage.

12 citations

mouseproteomics

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