Field-Programmable, Recombinase-Based Biomolecular Circuits: Difference between revisions
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{{Project | {{Project | ||
|Title=Field-Programmable, Recombinase-Based Circuits | |Title=Field-Programmable, Recombinase-Based Biomolecular Circuits | ||
|Agency= | |Agency=Army Research Office | ||
|Grant number=ICB-2019-SSB-02-Murray | |||
|Start date=1 Dec 2018 | |Start date=1 Dec 2018 | ||
|End date=30 Nov 2021 | |End date=30 Nov 2021 | ||
|Project ID= | |Support summary=1 graduate student, part-time technician | ||
|Reporting requirements=Annual reports | |||
|Project ID=AICB MRSB | |||
}} | }} | ||
Revision as of 22:20, 25 December 2018
Project description (typically about a paragraph)
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Current participants: Additional participants: |
Collaborators: Past participants:
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Objectives
Description of the main objectives of the project
References
- Addressable and adaptable intercellular communication via DNA messaging. John P. Marken and Richard M. Murray. Nature Communications, 14:2358, 2023.
- Integrase-mediated differentiation circuits improve evolutionary stability of burdensome and toxic functions in E. coli. Rory L. Williams and Richard M. Murray. Nature Communications, 13:6822, 2022.
- Tunable integrase-mediated differentiation facilitates improved output of burdensome functions in E. coli. Rory L. Williams, Richard M. Murray. bioRxiv 614529, 2019 (revised 2020, 2022).
- Addressable, “Packet-Based” Intercellular Communication through Plasmid Conjugation. John P. Marken, Richard M. Murray. qBio 2019 Conference.
- Proof of concept continuous event logging in living cells. Andrey Shur, Richard M. Murray. 2019 Synthetic Biology: Engineering, Evolution and Design (SEED) Conference.
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