Author

T. Mizuguchi

Yokohama City 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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Bioengineering· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Assay:imaging· 1 Research Focus:imputation· 1 Approach:microscopy & imaging analysis· 1 Organism:mouse· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Komazawa· 1 shared A. Kuechler· 1 shared A. Petersen· 1 shared A. Vaknin-Dembinsky· 1 shared A. Waheeb· 1 shared Adam JacksoniD· 1 shared Alexander J.M. DingemansiD· 1 shared Alexander P.A. StegmanniD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperBioengineering

A. Komazawa

Author profile →

2 papers

Recent·Most cited

Super-resolution vibrational imaging based on photoswitchable Raman probe

J. Shou, A. Komazawa, Y. Wachi, M. Kawatani, H. Fujioka, S. J. Spratt, T. Mizuguchi, K. Oguchi, F. Obata, R. Tachibana, Y. Misawa, R. Kojima, Y. Urano, M. Kamiya, Y. Ozeki

This paper introduces RESORT microscopy using photoswitchable Raman probes to achieve super-resolution vibrational imaging of live cells with high chemical specificity and spatial resolution.

bioRxiv · Aug 28, 2022Bioengineering

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Joery den Hoed, Elke de Boer, Norine Voisin, Alexander J.M. Dingemans, Nicolas Guex, Laurens Wiel, Christoffer Nellåker, Shivarajan Manickavasagam Amudhavalli, Siddarth Banka, Frederique Sloan Bena, Bruria Ben‐Zeev, Vincent Robert Bonagura, Ange‐Line Bruel, Theresa Brunet, Han G. Brunner, , Lisenka E.L.M. Vissers

The paper identifies mutation-specific pathophysiological mechanisms in SATB1 variants causing distinct neurodevelopmental disorders.

The American Journal of Human Genetics · Jan 28, 2021Peer-reviewedGenetics