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Jun Igarashi

Researcher at Nihon University

Publications -  17
Citations -  576

Jun Igarashi is an academic researcher from Nihon University. The author has contributed to research in topics: DNA methylation & Methylation. The author has an hindex of 11, co-authored 17 publications receiving 540 citations. Previous affiliations of Jun Igarashi include Roswell Park Cancer Institute.

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Genome-wide survey reveals dynamic widespread tissue-specific changes in DNA methylation during development

TL;DR: The data suggests the vast majority of unique sequence DNA methylation has tissue specificity, that demethylation has a prominent role in tissue differentiation, and that DNAmethylation has regulatory roles in alternative promoter selection and in non-promoter regions.
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Analysis of tissue-specific differentially methylated regions (TDMs) in humans.

TL;DR: It is indicated that some genomic regions with tissue-specific methylation and expression are conserved between mouse and human and suggest that DNA methylation may have an important role in regulating differentiation and tissue-/cell-specific gene expression of some genes.
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Inhibition of MMP‐9 transcription and suppression of tumor metastasis by pyrrole‐imidazole polyamide

TL;DR: A pyrrole-imidazole (PI) polyamide that targets the activator protein-1 (AP-1)-binding site of the MMP-9 promoter was designed and synthesized as a gene-silencing agent for tumor metastases as mentioned in this paper.
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Frequent trefoil factor 3 (TFF3) overexpression and promoter hypomethylation in mouse and human hepatocellular carcinomas.

TL;DR: The results indicate that TFF3 overexpression may be a critical process in mouse and human hepatocellular carcinogenesis, and the specific promoter CpG hypomethylation may be one of the regulation mechanisms of T FF3 overeexpression in HCCs.
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Quantitative analysis of human tissue-specific differences in methylation

TL;DR: DNA methylation levels of five testis-specific DMRs were significantly inversely correlated with the number of spermatocytes, but a positive correlation was seen at tDMRs located near the TRIM38 and CASZ1 genes.