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Ross D. Jones

Researcher at Massachusetts Institute of Technology

Publications -  18
Citations -  205

Ross D. Jones is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Synthetic biology & Medicine. The author has an hindex of 6, co-authored 13 publications receiving 102 citations. Previous affiliations of Ross D. Jones include University of Washington & University of British Columbia.

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An endoribonuclease-based feedforward controller for decoupling resource-limited genetic modules in mammalian cells.

TL;DR: An endoribonuclease-based feedforward controller is developed that can adapt the expression level of a gene of interest to significant resource loading in mammalian cells and is a general-purpose device for predictable, robust, and context-independent control of gene expression.
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A 'poly-transfection' method for rapid, one-pot characterization and optimization of genetic systems.

TL;DR: One-pot evaluation enabled by poly-transfection accelerates and simplifies the design of genetic systems, providing a new high-information strategy for interrogating biology.
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miRNA sensitivity to Drosha levels correlates with pre-miRNA secondary structure.

TL;DR: Statistical analysis of miRNA secondary structure and fold change of expression in response to Drosha knockdown showed that absence of mismatches in the central region of the hairpin, 5 and 9-12 nt from the Drosha cutting site conferred decreased sensitivity to Dro Sha knockdown, suggesting that, when limiting, Drosha processes miRNAs without mismatches more efficiently than mismatched mi RNAs.
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Context-aware synthetic biology by controller design: Engineering the mammalian cell.

TL;DR: In this article, the authors describe control systems approaches for achieving context-aware devices that are robust to context effects, and then consider cell fate programing as a case study to explore the potential impact of contextaware devices for regenerative medicine applications.
Journal Article

Effects of Antioxidants and Pro-oxidants on Cytotoxicity of Dihydroartemisinin to Molt-4 Human Leukemia Cells

TL;DR: Cellular oxidative status could alter the potency of artemisinin in killing cancer cells, and antioxidants would reduce, whereas pro-oxidants would enhance, cytotoxicity.