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Sachi Inukai

Researcher at Yale University

Publications -  13
Citations -  1032

Sachi Inukai is an academic researcher from Yale University. The author has contributed to research in topics: Gene & microRNA. The author has an hindex of 10, co-authored 12 publications receiving 821 citations. Previous affiliations of Sachi Inukai include Princeton University & Beth Israel Deaconess Medical Center.

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Journal ArticleDOI

Transcription factor–DNA binding: beyond binding site motifs

TL;DR: Novel approaches for characterizing functional binding site motifs that promise to inform the understanding of how TF binding controls gene expression and ultimately contributes to phenotype are highlighted.
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Age-associated changes in expression of small, noncoding RNAs, including microRNAs, in C. elegans.

TL;DR: This study suggests that sncRNAs including miRNAs contribute to lifespan regulation in C. elegans, and indicates new connections between aging, stress responses, and the small RNA world.
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Novel microRNAs differentially expressed during aging in the mouse brain.

TL;DR: The aging-affected brain miRNAs reported here may represent novel regulatory genes that also function during aging in the human brain, in agreement with trends observed in other miRNA studies in aging tissues and organisms.
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miR-34a Silences c-SRC to Attenuate Tumor Growth in Triple-Negative Breast Cancer

TL;DR: It is demonstrated that miR-34a exerts potent antitumorigenic effects in vitro and in vivo and suggests thatmiR- 34a replacement therapy, which is currently being tested in human clinical trials, represents a promising therapeutic strategy for TNBC.
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Survey of variation in human transcription factors reveals prevalent DNA binding changes

TL;DR: In this article, a computational, structure-based approach was developed to evaluate TF variants for their impact on DNA binding activity and used universal protein-binding microarrays to assay sequence-specific DNA binding activities across 41 reference and 117 variant alleles found in individuals of diverse ancestries and families with Mendelian diseases.