scispace - formally typeset
M

Mi Sook Chang

Researcher at California Institute of Technology

Publications -  14
Citations -  1501

Mi Sook Chang is an academic researcher from California Institute of Technology. The author has contributed to research in topics: RNA interference & RNA silencing. The author has an hindex of 8, co-authored 10 publications receiving 1439 citations. Previous affiliations of Mi Sook Chang include Stanford University.

Papers
More filters
Journal ArticleDOI

Synthetic dsRNA Dicer substrates enhance RNAi potency and efficacy.

TL;DR: These results provide an alternative strategy for eliciting RNAi-mediated target cleavage using low concentrations of synthetic RNA as substrates for cellular Dicer-mediated cleavage.
Journal ArticleDOI

Suppression of LPS-induced TNF-α production in macrophages by cAMP Is mediated by PKA-AKAP95-p105

TL;DR: Key anti-inflammatory effects of cAMP were mediated specifically by cAMP-dependent protein kinase (PKA), and selective inhibitors of PKA anchoring, time-lapse microscopy, and RNAi screening suggest that crosstalk between TLR4 and cAMP pathways in macrophages can be coordinated through PKA-dependent scaffolds that localize specific pools of the kinase to distinct substrates.
Journal ArticleDOI

Current issues for DNA microarrays: platform comparison, double linear amplification, and universal RNA reference

TL;DR: A comparison of several microarray platforms as well as analysis of various methods used for microarray target preparation and the reference design indicate that the pairwise correlations of expression levels between platforms are relative low overall but that the log ratios of the highly expressed genes are strongly correlated, especially between Affymetrix and cDNA arrays.
Journal ArticleDOI

A versatile approach to multiple gene RNA interference using microRNA-based short hairpin RNAs

TL;DR: A flexible platform using RNA polymerase II promoter-driven expression of microRNA-like short hairpin RNAs which permits robust depletion of multiple target genes from a single transcript and highlights the versatility of this vector platform for multiple target gene knockdown in mammalian cells.