Abstract
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Yuou Sheng, Huizhen Ni, Shihao Yang, Wenliang Hao
Abstract
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Provenance
crossref
Confidence 100%
openalex
Confidence 95%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
In vivo hypermutation and continuous evolution
10.1038/s43586-022-00119-5 · 2022
Directed evolution: methodologies and applications
10.1021/acs.chemrev.1c00260 · 2021
Scalable, continuous evolution of genes at mutation rates above genomic error thresholds
10.1016/j.cell.2018.10.021 · 2018
CRISPR-guided DNA polymerases enable diversification of all nucleotides in a tunable window
10.1038/s41586-018-0384-8 · 2018
OMEGA-guided DNA polymerases enable random mutagenesis in a tunable window
10.1016/j.tibtech.2025.02.011 · 2025
CRISPR-DNA polymerase assisted targeted mutagenesis for regulable laboratory evolution
2025
A Cas3-base editing tool for targetable in vivo mutagenesis
10.1038/s41467-023-39087-z · 2023
A processive protein chimera introduces mutations across defined DNA regions in vivo
10.1021/jacs.8b04001 · 2018
An orthogonal transcription mutation system generating all transition mutations for accelerated protein evolution in vivo
10.1038/s41467-025-61354-4 · 2025
The evolving story of the omega subunit of bacterial RNA polymerase
datacite
Confidence 0%
10.1016/j.tim.2006.08.002 · 2006
The Omega subunit of the RNA polymerase core directs transcription efficiency in cyanobacteria
10.1093/nar/gku084 · 2014
TracrRNA reprogramming enables direct PAM-independent detection of RNA with diverse DNA-targeting Cas12 nucleases
10.1038/s41467-024-50243-x · 2024
Miniature type V-F CRISPR-Cas nucleases enable targeted DNA modification in cells
10.1038/s41467-021-26469-4 · 2021
CRISPR-CasΦ from huge phages is a hypercompact genome editor
10.1126/science.abb1400 · 2020
RNA-guided DNA insertion with CRISPR-associated transposases
10.1126/science.aax9181 · 2019
Structural basis of target DNA recognition by CRISPR-Cas12k for RNA-guided DNA transposition
10.1016/j.molcel.2021.07.043 · 2021
Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression
10.1016/j.cell.2013.02.022 · 2013
Uracil accumulation and mutagenesis dominated by cytosine deamination in CpG dinucleotides in mice lacking UNG and SMUG1
10.1038/s41598-017-07314-5 · 2017
Structural basis of transcription: RNA polymerase backtracking and its reactivation
10.1016/j.molcel.2019.04.029 · 2019
Reciprocating RNA Polymerase batters through roadblocks
10.1038/s41467-024-47531-x · 2024
Structure and function of the transcription elongation factor GreB bound to bacterial RNA polymerase
10.1016/s0092-8674(03)00600-7 · 2003
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
10.1038/nature17946 · 2016
cutPrimers: a new tool for accurate cutting of primers from reads of targeted next generation sequencing
10.1089/cmb.2017.0096 · 2017
PANDAseq: paired-end assembler for illumina sequences
10.1186/1471-2105-13-31 · 2012
PANDAseq: paired-end assembler for illumina sequences
10.1186/1471-2105-13-31 · doi-reference
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
10.1038/nature17946 · doi-reference
Structure and function of the transcription elongation factor GreB bound to bacterial RNA polymerase
10.1016/s0092-8674(03)00600-7 · doi-reference
Reciprocating RNA Polymerase batters through roadblocks
10.1038/s41467-024-47531-x · doi-reference
Structural basis of transcription: RNA polymerase backtracking and its reactivation
10.1016/j.molcel.2019.04.029 · 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 · doi-reference
Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression
10.1016/j.cell.2013.02.022 · doi-reference
Structural basis of target DNA recognition by CRISPR-Cas12k for RNA-guided DNA transposition
10.1016/j.molcel.2021.07.043 · doi-reference
RNA-guided DNA insertion with CRISPR-associated transposases
10.1126/science.aax9181 · doi-reference
CRISPR-CasΦ from huge phages is a hypercompact genome editor
10.1126/science.abb1400 · doi-reference
Miniature type V-F CRISPR-Cas nucleases enable targeted DNA modification in cells
10.1038/s41467-021-26469-4 · doi-reference
TracrRNA reprogramming enables direct PAM-independent detection of RNA with diverse DNA-targeting Cas12 nucleases
10.1038/s41467-024-50243-x · doi-reference
The Omega subunit of the RNA polymerase core directs transcription efficiency in cyanobacteria
10.1093/nar/gku084 · doi-reference
The evolving story of the omega subunit of bacterial RNA polymerase
10.1016/j.tim.2006.08.002 · doi-reference
An orthogonal transcription mutation system generating all transition mutations for accelerated protein evolution in vivo
10.1038/s41467-025-61354-4 · doi-reference
cutPrimers: a new tool for accurate cutting of primers from reads of targeted next generation sequencing
10.1089/cmb.2017.0096 · doi-reference
A processive protein chimera introduces mutations across defined DNA regions in vivo
10.1021/jacs.8b04001 · doi-reference
A Cas3-base editing tool for targetable in vivo mutagenesis
10.1038/s41467-023-39087-z · doi-reference
OMEGA-guided DNA polymerases enable random mutagenesis in a tunable window
10.1016/j.tibtech.2025.02.011 · doi-reference
CRISPR-guided DNA polymerases enable diversification of all nucleotides in a tunable window
10.1038/s41586-018-0384-8 · doi-reference
Scalable, continuous evolution of genes at mutation rates above genomic error thresholds
10.1016/j.cell.2018.10.021 · doi-reference
Directed evolution: methodologies and applications
10.1021/acs.chemrev.1c00260 · doi-reference
In vivo hypermutation and continuous evolution
10.1038/s43586-022-00119-5 · doi-reference