about
Scalable Device for Automated Microbial Electroporation in a Digital Microfluidic Platform.Engineering posttranslational proofreading to discriminate nonstandard amino acids.The Future of Multiplexed Eukaryotic Genome Engineering.A CRISPR-Cas9-based gene drive platform for genetic interaction analysis in Candida albicans.Spontaneous CRISPR loci generation in vivo by non-canonical spacer integration.Cogenerating Synthetic Parts toward a Self-Replicating System.Adaptive evolution of genomically recoded Escherichia coli.Precise Cas9 targeting enables genomic mutation prevention.Establishing a Cell-Free Vibrio natriegens Expression SystemHigh-throughput creation and functional profiling of DNA sequence variant libraries using CRISPR-Cas9 in yeastBiosensor libraries harness large classes of binding domains for construction of allosteric transcriptional regulatorsDaisy-chain gene drives for the alteration of local populationsTerminator-free template-independent enzymatic DNA synthesis for digital information storage.Codon usage of highly expressed genes affects proteome-wide translation efficiencyData privacy in the age of personal genomicsAuthor Correction: Data privacy in the age of personal genomicsUnified rational protein engineering with sequence-based deep representation learningA single combination gene therapy treats multiple age-related diseasesSingle-Cell CRISPR-Based Lineage Tracing in MiceFunctional genomics of the rapidly replicating bacterium Vibrio natriegens by CRISPRiAn enhanced CRISPR repressor for targeted mammalian gene regulationImproved bacterial recombineering by parallelized protein discoveryA robust benchmark for detection of germline large deletions and insertions
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
George M Church
@en
George M Church
@nl
type
label
George M Church
@en
George M Church
@nl
prefLabel
George M Church
@en
George M Church
@nl
P31
P496
0000-0003-3535-2076