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Yuichiro Higashimoto

Researcher at Kurume University

Publications -  100
Citations -  7584

Yuichiro Higashimoto is an academic researcher from Kurume University. The author has contributed to research in topics: Heme & Glycation. The author has an hindex of 35, co-authored 98 publications receiving 7113 citations. Previous affiliations of Yuichiro Higashimoto include Saga Group & University of Texas Health Science Center at Tyler.

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PML regulates p53 acetylation and premature senescence induced by oncogenic Ras

TL;DR: It is found that oncogenic Ras upregulates PML expression, and overexpression of PML induces senescence in a p53-dependent manner, and integrity of the PML bodies is required for p53 acetylation and senescences upon oncogene expression.
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Homeodomain-interacting protein kinase-2 phosphorylates p53 at Ser 46 and mediates apoptosis

TL;DR: Homeodomain-interacting protein kinase-2 (HIPK2), a member of a novel family of nuclear serine/threonine kinases, binds to and activates p53 by directly phosphorylating it at Ser 46 and results in the targeted subcellular localization of p53 and initiation of apoptosis.
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MDM2–HDAC1-mediated deacetylation of p53 is required for its degradation

TL;DR: The results suggest that one major function of p53 acetylation is to promote p53 stability by preventingMDM2‐dependent ubiquitylation, while recruitment of HDAC1 by MDM2 promotes p53 degradation by removing these acetyl groups.
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Initiation of a G2/M checkpoint after ultraviolet radiation requires p38 kinase

TL;DR: It is reported that p38 kinase has a critical role in the initiation of a G2 delay after ultraviolet radiation, and regulation of Cdc25B phosphorylation by p38 is a critical event for initiating the G2/M checkpoint after ultraviolet Radiation.
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Nitric oxide-induced cellular stress and p53 activation in chronic inflammation.

TL;DR: In noncancerous colon tissues from patients with ulcerative colitis, inducible NO synthase protein levels were positively correlated with p53 serine 15 phosphorylation levels, and Immunostaining of HDM-2 and p21WAF1 was consistent with transcriptionally active p53.