A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
about
Tolerance of a Knotted Near-Infrared Fluorescent Protein to Random Circular PermutationAddressing biological uncertainties in engineering gene circuitsEngineering RGB color vision into Escherichia coliGenetic circuit design automation.Combining random gene fission and rational gene fusion to discover near-infrared fluorescent protein fragments that report on protein-protein interactions.The Structure of a Thermophilic Kinase Shapes Fitness upon Random Circular PermutationPERMutation Using Transposase Engineering (PERMUTE): A Simple Approach for Constructing Circularly Permuted Protein Libraries.Role of Autoregulation and Relative Synthesis of Operon Partners in Alternative Sigma Factor Networks.Rapid generation of CRISPR/dCas9-regulated, orthogonally repressible hybrid T7-lac promoters for modular, tuneable control of metabolic pathway fluxes in Escherichia coliEnhanced Promoter Activity by Replenishment of Sigma Factor rpoE in Klebsiella pneumoniae.Post-translational control of genetic circuits using Potyvirus proteases.Engineering microbial hosts for production of bacterial natural productsA split intein T7 RNA polymerase for transcriptional AND-logic.Synthetic biology: the many facets of T7 RNA polymerase.A portable expression resource for engineering cross-species genetic circuits and pathways.Standardization in synthetic biology: an engineering discipline coming of age.Synthetic Gene Expression Circuits for Designing Precision Tools in Oncology.Fundamental CRISPR-Cas9 tools and current applications in microbial systems.Targeted mutagenesis: A sniper-like diversity generator in microbial engineering.Synthetic Gene Expression Circuits for Designing Precision Tools in Oncology.A sigma factor toolbox for orthogonal gene expression in Escherichia coli.RNA Polymerase Tags To Monitor Multidimensional Protein-Protein Interactions Reveal Pharmacological Engagement of Bcl-2 Proteins.Dynamic allocation of orthogonal ribosomes facilitates uncoupling of co-expressed genes.Development of cyclic AMP receptor protein-based artificial transcription factor for intensifying gene expression.Programmed hierarchical patterning of bacterial populations.Evolution of a split RNA polymerase as a versatile biosensor platform.Promoter and Terminator Discovery and Engineering.Viral attenuation by engineered protein fragmentation.
P2860
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P2860
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@ast
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@en
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@nl
type
label
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@ast
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@en
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@nl
prefLabel
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@ast
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@en
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.
@nl
P2093
P2860
P356
P1476
A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase
@en
P2093
Adam J Meyer
Andrew D Ellington
Christopher A Voigt
Eduardo D Sontag
P2860
P356
10.15252/MSB.20145299
P577
2014-07-30T00:00:00Z