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Keiko Tano

Researcher at University of Tokyo

Publications -  12
Citations -  1461

Keiko Tano is an academic researcher from University of Tokyo. The author has contributed to research in topics: Gene & Induced pluripotent stem cell. The author has an hindex of 10, co-authored 12 publications receiving 1254 citations. Previous affiliations of Keiko Tano include National Institutes of Health.

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MALAT-1 enhances cell motility of lung adenocarcinoma cells by influencing the expression of motility-related genes

TL;DR: It is suggested that MALAT‐1 is a novel class of non‐coding RNA that promotes cell motility through transcriptional and post‐transcriptional regulation of motility related gene expression.
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Genome-wide determination of RNA stability reveals hundreds of short-lived noncoding transcripts in mammals

TL;DR: This study determined the half-lives of 11,052 mRNAs and 1418 ncRNAs in HeLa Tet-off (TO) cells by developing a novel genome-wide method, which was named 5'-bromo-uridine immunoprecipitation chase-deep sequencing analysis (BRIC-seq), and identified and characterized several novel long nCRNAs involved in cell proliferation from the group of short-lived nc RNAs.
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Long non-coding RNAs in cancer progression

TL;DR: A review of recent findings regarding the roles of lncRNAs in cancer biology highlights the importance of knowing the underlying molecular mechanisms by which these molecules regulate cancer development.
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Identification of cis- and trans-acting factors involved in the localization of MALAT-1 noncoding RNA to nuclear speckles

TL;DR: It is suggested that RNPS1, SRm160, and IBP160 contribute to the localization of MALat-1 to nuclear speckles, where MALAT-1 could be involved in regulating gene expression.
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Identification and Characterization of Novel Genotoxic Stress-Inducible Nuclear Long Noncoding RNAs in Mammalian Cells

TL;DR: The results suggest that distinct sets of nuclear long ncRNAs play roles in cellular defense mechanisms against specific genotoxic agents, and that particular long nCRNAs have the potential to be surrogate indicators of a specific cell stress.