Author

H. Hashimoto

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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Biochemistry· 2 Cell Biology· 2 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:human· 4 Research Focus:cell type annotation· 2 Research Focus:protein structure prediction· 2 Assay:structural biology· 2 Assay:electrophysiology· 1 Assay:imaging· 1 Organism:mouse· 1

Frequent Co-Authors

E. W. Debler· 2 shared A. Kasai· 1 shared A. Raczkowski· 1 shared B. PALANCADE· 1 shared D. H. Ramirez· 1 shared G. Blobel· 1 shared H. Kishima· 1 shared H. M. Khoo· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 11 mutual co-author links

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2 shared papersBiochemistry

E. W. Debler

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Author profile →

5 papers

Recent·Most cited

Structure of the pre-mRNA leakage 39-kDa proteinreveals a single domain of integrated zf-C3HC and Rsm1 modules

H. Hashimoto, D. H. Ramirez, O. Lautier, N. Pawlak, G. Blobel, B. PALANCADE, E. W. Debler

The paper determines the crystal structure of ScPml39, revealing integrated zf-C3HC and Rsm1 modules and identifies structural orthologs in S. pombe and humans.

bioRxiv · Aug 11, 2022Biochemistry

Frequency band coupling with high-frequency activities during seizures shifts from θ band in tonic phase to δ band in clonic phase

H. Hashimoto, H. M. Khoo, T. Yanagisawa, N. Tani, S. Oshino, M. Hirata, H. Kishima

This paper analyzes how high-frequency activities (HFAs) couple with low-frequency bands during seizures, finding that coupling shifts from theta to delta bands during the tonic to clonic phase.

bioRxiv · Oct 6, 2021 · PreprintPhysiology

Exploring rare cellular activity in more than one million cells by a trans-scale-scope

T. Ichimura, T. Kakizuka, K. Horikawa, K. Seiriki, A. Kasai, H. Hashimoto, K. Fujita, T. M. Watanabe, T. Nagai

The paper introduces an imaging system to observe rare cellular activity in over one million cells and demonstrates its ability to detect rare events in biological systems.

bioRxiv · Jun 29, 2020 · PreprintCell Biology

Structural Basis of Protein Arginine Methyltransferase Activation by a Catalytically Dead Homolog (Prozyme)

H. Hashimoto, L. Kafkova, A. Raczkowski, K. D. Jordan, L. K. Read, E. W. Debler

This paper reports the crystal structure of a Trypanosoma brucei PRMT1 enzyme-prozyme heterotetramer, revealing how the prozyme stabilizes the enzyme and enables catalysis through structural and functional interactions.

bioRxiv · Sep 19, 2019Biochemistry

Structural basis of HEAT-kleisin interactions in the human condensin I subcomplex

K. Hara, K. Kinoshita, T. Migita, K. Murakami, K. Shimizu, K. Takeuchi, T. Hirano, H. Hashimoto

This study reports the crystal structure of the human condensin I subcomplex hCAP-G and hCAP-H, revealing their interaction and DNA binding capabilities essential for mitotic chromosome assembly.

bioRxiv · Oct 4, 2018Cell Biology