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Huili Guo

Researcher at Agency for Science, Technology and Research

Publications -  19
Citations -  9170

Huili Guo is an academic researcher from Agency for Science, Technology and Research. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 8, co-authored 11 publications receiving 8327 citations. Previous affiliations of Huili Guo include Massachusetts Institute of Technology & Institute of Molecular and Cell Biology.

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Mammalian microRNAs predominantly act to decrease target mRNA levels

TL;DR: Results show that changes in mRNA levels closely reflect the impact of miRNAs on gene expression and indicate that destabilization of target mRNAs is the predominant reason for reduced protein output.
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Mammalian microRNAs predominantly act to decrease target mRNA levels

TL;DR: In this paper, the authors used ribosome profiling to measure the overall effects on protein production and compare these to simultaneously measured effects on mRNA levels, showing that changes in mRNA levels closely reflect the impact of miRNAs on gene expression and indicate that destabilization of target mRNAs is the predominant reason for reduced protein output.
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Expanded identification and characterization of mammalian circular RNAs

TL;DR: A computational pipeline to identifycircRNAs and quantify their relative abundance from RNA-seq data is developed, providing a new framework for future investigation of this intriguing topological isoform while raising doubts regarding a biological function of most circRNAs.
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mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues.

TL;DR: The global steady-state measurements are extended to additional mammalian contexts and find that regardless of the miRNA, cell type, growth condition, or translational state, mRNA destabilization explains most (66%->90%) miRNA-mediated repression.
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The Drosophila hairpin RNA pathway generates endogenous short interfering RNAs.

TL;DR: It is reported that siRNAs derived from long hairpin RNA genes (hpRNAs) programme Slicer complexes that can repress endogenous target transcripts and reveal unexpected complexity in the sorting of small RNAs in Drosophila.