Author

T. Kojidani

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· 2

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Organism:fungi (other)· 1 Assay:imaging· 1 Approach:microscopy & imaging analysis· 1 Assay:proteomics· 1 Organism:yeast· 1

Frequent Co-Authors

T. Haraguchi· 2 shared Y. Hiraoka· 2 shared A. Matsuda· 1 shared C. Obuse· 1 shared C. Ohtsuki· 1 shared C. Spanos· 1 shared E. Lynch· 1 shared H. Asakawa· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersCell Biology

T. Haraguchi

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2 papers

Recent·Most cited

Asymmetrical localization of Nup107-160 subcomplex components within the nuclear pore complex in fission yeast

H. Asakawa, T. Kojidani, H.-J. Yang, C. Ohtsuki, H. Osakada, A. Matsuda, M. Iwamoto, Y. Chikashige, K. Nagao, C. Obuse, Y. Hiraoka, T. Haraguchi

This study reveals asymmetrical localization of the Nup107-160 subcomplex in fission yeast, contrasting with symmetrical localization in other organisms, and shows its necessity for cell cycle progression.

bioRxiv · Feb 28, 2019Cell Biology

Exportin Crm1 is repurposed as a docking protein to generate microtubule organizing centers at the nuclear pore

X. Bao, C. Spanos, T. Kojidani, E. Lynch, J. Rappsilber, Y. Hiraoka, T. Haraguchi, K. Sawin

The paper identifies how Mto1 docks at nuclear pore complexes via Crm1 and Nup146 to form non-centrosomal MTOCs.

bioRxiv · Nov 9, 2017Cell Biology