Author

Masamitsu Nishi

Hyogo Medical University

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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Molecular Biology· 2

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Harutoshi Fujimura· 2 shared Kenji Jinnai· 2 shared Masataka IgetaiD· 2 shared Takashi KimuraiD· 2 shared Tsuyoshi MatsumuraiD· 2 shared Hiroo Yoshikawa· 1 shared Kazuki YoshizumiiD· 1 shared Koichi Suenaga· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersMolecular Biology

Harutoshi Fujimura

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2 papers

Recent·Most cited

Analysis of splicing abnormalities in the white matter of myotonic dystrophy type 1 brain using RNA-sequence

Kazuki Yoshizumi, Masamitsu Nishi, Masataka Igeta, Masayuki Nakamori, Tsuyoshi Matsumura, Harutoshi Fujimura, Kenji Jinnai, Takashi Kimura

This study investigates splicing abnormalities in white matter of DM1 brains using RNA-seq, finding that WM defects may result from both GM and WM RNA splicing issues.

bioRxiv · Dec 23, 2022 · PreprintMolecular Biology

Differences in splicing defects between the grey and white matter in myotonic dystrophy type 1

Masamitsu Nishi, Takashi Kimura, Masataka Igeta, Mitsuru Furuta, Koichi Suenaga, Tsuyoshi Matsumura, Harutoshi Fujimura, Kenji Jinnai, Hiroo Yoshikawa

The paper examines splicing defects in grey and white matter of DM1 patients, finding greater PSI changes in grey matter compared to white matter.

PLoS ONE · May 14, 2020Peer-reviewedMolecular Biology