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Hiroshi Sakai

Researcher at Pasteur Institute

Publications -  143
Citations -  2460

Hiroshi Sakai is an academic researcher from Pasteur Institute. The author has contributed to research in topics: Gene & DNA replication. The author has an hindex of 26, co-authored 141 publications receiving 2172 citations. Previous affiliations of Hiroshi Sakai include Centre national de la recherche scientifique & Tokyo Institute of Technology.

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High-Dimensional Single-Cell Cartography Reveals Novel Skeletal Muscle-Resident Cell Populations

TL;DR: Ten different mononuclear cell types in adult mouse muscle are mapped using a combined approach of single-cell RNA sequencing and mass cytometry to yield crucial insights into muscle-resident cell-type identities and can be exploited to study muscle diseases.
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Injury-Induced Senescence Enables In Vivo Reprogramming in Skeletal Muscle

TL;DR: It is shown that acute and chronic injury enables transcription-factor-mediated reprogramming in skeletal muscle and this response frequently originates from Pax7+ muscle stem cells, highlighting a beneficial paracrine effect of injury-induced senescence on cellular plasticity.
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Chromatin signatures at Notch-regulated enhancers reveal large-scale changes in H3K56ac upon activation

TL;DR: While many histone modifications were unchanged by Su(H) binding or Notch activation, rapid changes in acetylation of H3K56 at Notch‐regulated enhancers appear to be a conserved indicator of enhancer activation.
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In Vitro Modeling of Paraxial Mesodermal Progenitors Derived from Induced Pluripotent Stem Cells

TL;DR: A protocol for the differentiation of mouse iPS cells into paraxial mesodermal lineages in serum-free culture was established and exhibited differentiation potential into osteogenic, chondrogenic, and myogenic cells both in vitro and in vivo and contributed to muscle regeneration.
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Mossbauer Spectroscopic Study of Iodine-Doped Polyacetylene

TL;DR: In this article, the Mossbauer spectroscopy has been applied to iodine-doped polyacetylene employing 129 I. It is found that the polymer films contain I -, I 3 - and I 5 - with symmetrical charge population, where the content of each iodide anion depends on the doping level.