Research graph
References from Hijacking host RNA polymerase for processive in situ mutagenesis. Local targets link to admitted publications; unresolved targets remain external evidence.
In vivo hypermutation and continuous evolution
10.1038/s43586-022-00119-5 · 2022 · External reference
Directed evolution: methodologies and applications
10.1021/acs.chemrev.1c00260 · 2021 · External reference
Scalable, continuous evolution of genes at mutation rates above genomic error thresholds
10.1016/j.cell.2018.10.021 · 2018 · External reference
CRISPR-guided DNA polymerases enable diversification of all nucleotides in a tunable window
10.1038/s41586-018-0384-8 · 2018 · External reference
OMEGA-guided DNA polymerases enable random mutagenesis in a tunable window
10.1016/j.tibtech.2025.02.011 · 2025 · External reference
CRISPR-DNA polymerase assisted targeted mutagenesis for regulable laboratory evolution
2025 · External reference
A Cas3-base editing tool for targetable in vivo mutagenesis
10.1038/s41467-023-39087-z · 2023 · External reference
A processive protein chimera introduces mutations across defined DNA regions in vivo
10.1021/jacs.8b04001 · 2018 · External reference
An orthogonal transcription mutation system generating all transition mutations for accelerated protein evolution in vivo
10.1038/s41467-025-61354-4 · 2025 · External reference
The evolving story of the omega subunit of bacterial RNA polymerase
10.1016/j.tim.2006.08.002 · 2006 · External reference
The Omega subunit of the RNA polymerase core directs transcription efficiency in cyanobacteria
10.1093/nar/gku084 · 2014 · External reference
TracrRNA reprogramming enables direct PAM-independent detection of RNA with diverse DNA-targeting Cas12 nucleases
10.1038/s41467-024-50243-x · 2024 · External reference
Miniature type V-F CRISPR-Cas nucleases enable targeted DNA modification in cells
10.1038/s41467-021-26469-4 · 2021 · External reference
CRISPR-CasΦ from huge phages is a hypercompact genome editor
10.1126/science.abb1400 · 2020 · External reference
RNA-guided DNA insertion with CRISPR-associated transposases
10.1126/science.aax9181 · 2019 · External reference
Structural basis of target DNA recognition by CRISPR-Cas12k for RNA-guided DNA transposition
10.1016/j.molcel.2021.07.043 · 2021 · External reference
Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression
10.1016/j.cell.2013.02.022 · 2013 · External reference
Uracil accumulation and mutagenesis dominated by cytosine deamination in CpG dinucleotides in mice lacking UNG and SMUG1
10.1038/s41598-017-07314-5 · 2017 · External reference
Structural basis of transcription: RNA polymerase backtracking and its reactivation
10.1016/j.molcel.2019.04.029 · 2019 · External reference
Reciprocating RNA Polymerase batters through roadblocks
10.1038/s41467-024-47531-x · 2024 · External reference
Structure and function of the transcription elongation factor GreB bound to bacterial RNA polymerase
10.1016/s0092-8674(03)00600-7 · 2003 · External reference
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
10.1038/nature17946 · 2016 · External reference
cutPrimers: a new tool for accurate cutting of primers from reads of targeted next generation sequencing
10.1089/cmb.2017.0096 · 2017 · External reference
PANDAseq: paired-end assembler for illumina sequences
10.1186/1471-2105-13-31 · 2012 · External reference
Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression
10.1016/j.cell.2013.02.022 · ExternalCitation · doi-reference
Scalable, continuous evolution of genes at mutation rates above genomic error thresholds
10.1016/j.cell.2018.10.021 · ExternalCitation · doi-reference
Structural basis of transcription: RNA polymerase backtracking and its reactivation
10.1016/j.molcel.2019.04.029 · ExternalCitation · doi-reference
Structural basis of target DNA recognition by CRISPR-Cas12k for RNA-guided DNA transposition
10.1016/j.molcel.2021.07.043 · ExternalCitation · doi-reference
OMEGA-guided DNA polymerases enable random mutagenesis in a tunable window
10.1016/j.tibtech.2025.02.011 · ExternalCitation · doi-reference
The evolving story of the omega subunit of bacterial RNA polymerase
10.1016/j.tim.2006.08.002 · ExternalCitation · doi-reference
Structure and function of the transcription elongation factor GreB bound to bacterial RNA polymerase
10.1016/s0092-8674(03)00600-7 · ExternalCitation · doi-reference
Directed evolution: methodologies and applications
10.1021/acs.chemrev.1c00260 · ExternalCitation · doi-reference
A processive protein chimera introduces mutations across defined DNA regions in vivo
10.1021/jacs.8b04001 · ExternalCitation · doi-reference
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
10.1038/nature17946 · ExternalCitation · doi-reference
Miniature type V-F CRISPR-Cas nucleases enable targeted DNA modification in cells
10.1038/s41467-021-26469-4 · ExternalCitation · doi-reference
A Cas3-base editing tool for targetable in vivo mutagenesis
10.1038/s41467-023-39087-z · ExternalCitation · doi-reference
Reciprocating RNA Polymerase batters through roadblocks
10.1038/s41467-024-47531-x · ExternalCitation · doi-reference
TracrRNA reprogramming enables direct PAM-independent detection of RNA with diverse DNA-targeting Cas12 nucleases
10.1038/s41467-024-50243-x · ExternalCitation · doi-reference
An orthogonal transcription mutation system generating all transition mutations for accelerated protein evolution in vivo
10.1038/s41467-025-61354-4 · ExternalCitation · doi-reference
CRISPR-guided DNA polymerases enable diversification of all nucleotides in a tunable window
10.1038/s41586-018-0384-8 · ExternalCitation · doi-reference
Uracil accumulation and mutagenesis dominated by cytosine deamination in CpG dinucleotides in mice lacking UNG and SMUG1
10.1038/s41598-017-07314-5 · ExternalCitation · doi-reference
In vivo hypermutation and continuous evolution
10.1038/s43586-022-00119-5 · ExternalCitation · doi-reference
cutPrimers: a new tool for accurate cutting of primers from reads of targeted next generation sequencing
10.1089/cmb.2017.0096 · ExternalCitation · doi-reference
The Omega subunit of the RNA polymerase core directs transcription efficiency in cyanobacteria
10.1093/nar/gku084 · ExternalCitation · doi-reference
RNA-guided DNA insertion with CRISPR-associated transposases
10.1126/science.aax9181 · ExternalCitation · doi-reference
CRISPR-CasΦ from huge phages is a hypercompact genome editor
10.1126/science.abb1400 · ExternalCitation · doi-reference
PANDAseq: paired-end assembler for illumina sequences
10.1186/1471-2105-13-31 · ExternalCitation · doi-reference
