Current and future prospects for CRISPR-based tools in bacteria
about
Scarless deletion of up to seven methyl-accepting chemotaxis genes with an optimized method highlights key function of CheM in Salmonella Typhimurium.New tools for reconstruction and heterologous expression of natural product biosynthetic gene clusters.The CRISPR RNA-guided surveillance complex in Escherichia coli accommodates extended RNA spacersA CRISPR-Cas9 Assisted Non-Homologous End-Joining Strategy for One-step Engineering of Bacterial Genome.Toward a genetic tool development pipeline for host-associated bacteria.Epigenetic Treatment of Persistent Viral Infections.Deciphering, Communicating, and Engineering the CRISPR PAM.CRISPR-Cas Systems Features and the Gene-Reservoir Role of Coagulase-Negative Staphylococci.Harnessing heterologous and endogenous CRISPR-Cas machineries for efficient markerless genome editing in ClostridiumCas9 Nickase-Assisted RNA Repression Enables Stable and Efficient Manipulation of Essential Metabolic Genes in Clostridium cellulolyticum.CRISPR-Cas12a-Assisted Recombineering in Bacteria.Cas9-mediated genome editing in the methanogenic archaeon Methanosarcina acetivorans.Advances and Obstacles in the Genetic Dissection of Chlamydial Virulence.Challenges and Advances for Genetic Engineering of Non-model Bacteria and Uses in Consolidated Bioprocessing.Stimulation of reverse transcriptase generated cDNAs with specific indels by template RNA structure: retrotransposon, dNTP balance, RT-reagent usage.Single plasmid systems for inducible dual protein expression and for CRISPR-Cas9/CRISPRi gene regulation in lactic acid bacterium Lactococcus lactis.Emerging Nanomedicine Therapies to Counter the Rise of Methicillin-Resistant Staphylococcus aureus.Scarless Cas9 Assisted Recombineering (no-SCAR) in Escherichia coli, an Easy-to-Use System for Genome Editing.Development of a bacterial-based negative selection system for rapid screening of active single guide RNAs.Silk Route to the Acceptance and Re-Implementation of Bacteriophage Therapy-Part II.Genome editing of Ralstonia eutropha using an electroporation-based CRISPR-Cas9 technique.
P2860
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P2860
Current and future prospects for CRISPR-based tools in bacteria
description
2016 nî lūn-bûn
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2016 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2016 թվականի մայիսին հրատարակված գիտական հոդված
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年學術文章
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name
Current and future prospects for CRISPR-based tools in bacteria
@ast
Current and future prospects for CRISPR-based tools in bacteria
@en
Current and future prospects for CRISPR-based tools in bacteria
@nl
type
label
Current and future prospects for CRISPR-based tools in bacteria
@ast
Current and future prospects for CRISPR-based tools in bacteria
@en
Current and future prospects for CRISPR-based tools in bacteria
@nl
prefLabel
Current and future prospects for CRISPR-based tools in bacteria
@ast
Current and future prospects for CRISPR-based tools in bacteria
@en
Current and future prospects for CRISPR-based tools in bacteria
@nl
P2860
P921
P3181
P356
P1476
Current and future prospects for CRISPR-based tools in bacteria
@en
P2093
Michelle L Luo
Ryan T Leenay
P2860
P304
P3181
P356
10.1002/BIT.25851
P407
P577
2015-10-27T00:00:00Z