Hiroshi Kimura - Nanotechnology

Author Information

Hiroshi Kimura is affiliated with the Cell Biology Center at the Institute of Innovative Research, Tokyo Institute of Technology, located in Yokohama, Japan. His research primarily focuses on cellular and molecular biology, with a keen interest in transcription dynamics, histone modifications, and live-cell imaging techniques.

Research Contributions

Hiroshi Kimura has made significant contributions to the field of cell biology, particularly in understanding the mechanisms of transcription elongation and the spatial organization of transcriptional activity. His work has provided insights into the dynamics of RNA polymerase II phosphorylation, the role of ubiquitination in gene repression, and the structural basis of histone modifications. In 2022 alone, Kimura published several influential papers on topics such as the STREAMING-tag system, single-cell profiling of transcriptome and histone modifications, and live imaging of transcription sites.

Aliases

Hiroshi Kimura is also known by the aliases H Kimura, H. Kimura, and H. Kimura.

Publication and Citation Metrics

Metric	Value
Citation Count	18,978
h-index	72
Paper Count	383

Publications:

Imaging transcription elongation dynamics by new technologies unveils the organization of initiation and elongation in transcription factories.

DOI: 10.1016/j.ceb.2022.01.002

Year: 2022

A Drosophila toolkit for HA-tagged proteins unveils a block in autophagy flux in the last instar larval fat body.

DOI: 10.1242/dev.200243

Year: 2022

STREAMING-tag system reveals spatiotemporal relationships between transcriptional regulatory factors and transcriptional activity

DOI: 10.1101/2022.01.06.472721

Year: 2022

Single-cell profiling of transcriptome and histone modifications with EpiDamID.

DOI: 10.1016/j.molcel.2022.03.009

Year: 2022

Nucleoplasmic Lamin C Rapidly Accumulates at Sites of Nuclear Envelope Rupture with BAF and cGAS

DOI: 10.1101/2022.01.05.475028

Year: 2022

Live imaging of transcription sites using an elongating RNA polymerase II–specific probe

DOI: 10.1083/jcb.202104134

Year: 2022

Attrition of X Chromosome Inactivation in Aged Hematopoietic Stem Cells

DOI: 10.1016/j.stemcr.2021.03.007

Year: 2021

Ubiquitination‐dependent and ‐independent repression of target genes by SETDB1 reveal a context‐dependent role for its methyltransferase activity during adipogenesis

DOI: 10.1111/gtc.12868

Year: 2021

Live-cell imaging reveals the spatiotemporal organization of endogenous RNA polymerase II phosphorylation at a single gene

DOI: 10.1101/2020.04.03.024414

Year: 2021

Structural basis of nucleosomal histone H4 lysine 20 methylation by SET8 methyltransferase

DOI: 10.26508/lsa.202000919

Year: 2021

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