Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems - Wikidata - awgldk - TriplyDB

Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

http://www.wikidata.org/entity/Q30740166

about

DNA binding specificities of Escherichia coli Cas1-Cas2 integrase drive its recruitment at the CRISPR locus CRISPR-Cpf1 assisted genome editing of Corynebacterium glutamicum.Multiplex gene regulation by CRISPR-ddCpf1 Applications of CRISPR technologies in research and beyond.Evolution of RNA- and DNA-guided antivirus defense systems in prokaryotes and eukaryotes: common ancestry vs convergence Comparative genomic analysis identifies structural features of CRISPR-Cas systems in Riemerella anatipestifer.Coupling immunity and programmed cell suicide in prokaryotes: Life-or-death choices.The CRISPR RNA-guided surveillance complex in Escherichia coli accommodates extended RNA spacers DNA Targeting by a Minimal CRISPR RNA-Guided Cascade.Toward a genetic tool development pipeline for host-associated bacteria.Deciphering, Communicating, and Engineering the CRISPR PAM.A decade of discovery: CRISPR functions and applications.Programmable transcriptional repression in mycobacteria using an orthogonal CRISPR interference platform.Long-term genomic coevolution of host-parasite interaction in the natural environment.CRISPR-Cas12a-Assisted Recombineering in Bacteria.Interference-driven spacer acquisition is dominant over naive and primed adaptation in a native CRISPR-Cas system.High-Throughput Characterization of Cascade type I-E CRISPR Guide Efficacy Reveals Unexpected PAM Diversity and Target Sequence Preferences.Real-Time Observation of Target Search by the CRISPR Surveillance Complex Cascade.Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum.FnCpf1: a novel and efficient genome editing tool for Saccharomyces cerevisiae.Rapid and Scalable Characterization of CRISPR Technologies Using an E. coli Cell-Free Transcription-Translation System.Bacteriophage DNA glucosylation impairs target DNA binding by type I and II but not by type V CRISPR-Cas effector complexes.Methods and Applications of CRISPR-Mediated Base Editing in Eukaryotic Genomes.A 'new lease of life': FnCpf1 possesses DNA cleavage activity for genome editing in human cells.Massively Parallel Biophysical Analysis of CRISPR-Cas Complexes on Next Generation Sequencing Chips.Priming in a permissive type I-C CRISPR-Cas system reveals distinct dynamics of spacer acquisition and loss.Lactobacillus gasseri CRISPR-Cas9 characterization In Vitro reveals a flexible mode of protospacer-adjacent motif recognition.SaCas9 Requires 5'-NNGRRT-3' PAM for Sufficient Cleavage and Possesses Higher Cleavage Activity than SpCas9 or FnCpf1 in Human Cells.Determining the Specificity of Cascade Binding, Interference, and Primed Adaptation In Vivo in the Escherichia coli Type I-E CRISPR-Cas System.Cas4-Dependent Prespacer Processing Ensures High-Fidelity Programming of CRISPR Arrays.Designing Epigenome Editors: Considerations of Biochemical and Locus Specificities.A detailed cell-free transcription-translation-based assay to decipher CRISPR protospacer-adjacent motifs.CRISPR RNA-Dependent Binding and Cleavage of Endogenous RNAs by the Campylobacter jejuni Cas9.Precise Excision of the CAG Tract from the Huntingtin Gene by Cas9 Nickases.Gene repression via multiplex gRNA strategy in Y. lipolytica.CRISPR-Cas adaptation in Escherichia coli requires RecBCD helicase but not nuclease activity, is independent of homologous recombination, and is antagonized by 5' ssDNA exonucleases Minimal PAM specificity of a highly similar SpCas9 ortholog Mb- and FnCpf1 nucleases are active in mammalian cells: activities and PAM preferences of four wild-type Cpf1 nucleases and of their altered PAM specificity variants Class 2 CRISPR/Cas: an expanding biotechnology toolbox for and beyond genome editing

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P2860

Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

http://www.wikidata.org/entity/Q30740166

description

2016 nî lūn-bûn

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2016 թուականի Մարտին հրատարակուած գիտական յօդուած

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2016 թվականի մարտին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

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Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

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type

label

Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

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Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

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prefLabel

Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

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Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

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J.MOLCEL.2016.02.031

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Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

@en

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Ahmed A Gomaa

http://www.w3.org/2001/XMLSchema#string

Kenneth R Maksimchuk

http://www.w3.org/2001/XMLSchema#string

Rebecca A Slotkowski

http://www.w3.org/2001/XMLSchema#string

Roma N Agrawal

http://www.w3.org/2001/XMLSchema#string

Ryan T Leenay

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P2860

Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems

CRISPR Provides Acquired Resistance Against Viruses in Prokaryotes

RNA-guided human genome engineering via Cas9

Multiplex genome engineering using CRISPR/Cas systems

CRISPR RNA maturation by trans-encoded small RNA and host factor RNase III

RNA-guided editing of bacterial genomes using CRISPR-Cas systems

Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system

A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity

Cas5d Protein Processes Pre-crRNA and Assembles into a Cascade-like Interference Complex in Subtype I-C/Dvulg CRISPR-Cas System

Structural basis of PAM-dependent target DNA recognition by the Cas9 endonuclease

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137-147

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scholarly article

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10.1016/J.MOLCEL.2016.02.031

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1

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62

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Rodolphe Barrangou

Alexandra E Briner

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2016-03-30T00:00:00Z

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27041224

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4826307

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