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Volumn 361, Issue 6408, 2018, Pages 1259-1262
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Engineered CRISPR-Cas9 nuclease with expanded targeting space
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KEIO UNIVERSITY
(Japan)
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Author keywords
[No Author keywords available]
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Indexed keywords
CRISPR ASSOCIATED PROTEIN;
CYTIDINE DEAMINASE;
NUCLEIC ACID BASE;
BACTERIAL PROTEIN;
CAS9 ENDONUCLEASE STREPTOCOCCUS PYOGENES;
ENDONUCLEASE;
BIOENGINEERING;
CELL;
CRYSTAL STRUCTURE;
DNA;
GENE;
GENE EXPRESSION;
GENOMICS;
ARTICLE;
CONTROLLED STUDY;
CRISPR-CAS9 SYSTEM;
CRYSTAL STRUCTURE;
ENZYME ACTIVATION;
GENE MUTATION;
GENE TARGETING;
GENETIC ENGINEERING;
GENETIC VARIABILITY;
HUMAN;
HUMAN CELL;
PRIORITY JOURNAL;
PROTEIN CLEAVAGE;
PROTEIN DEPLETION;
PROTEIN DNA INTERACTION;
PROTEIN MOTIF;
PROTEIN TARGETING;
WILD TYPE;
CHEMISTRY;
CRISPR CAS SYSTEM;
GENE EDITING;
GENETICS;
HEK293 CELL LINE;
PROTEIN ENGINEERING;
X RAY CRYSTALLOGRAPHY;
STREPTOCOCCUS PYOGENES;
BACTERIAL PROTEINS;
CRISPR-CAS SYSTEMS;
CRYSTALLOGRAPHY, X-RAY;
ENDONUCLEASES;
GENE EDITING;
HEK293 CELLS;
HUMANS;
PROTEIN ENGINEERING;
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EID: 85054018722
PISSN: 00368075
EISSN: 10959203
Source Type: Journal
DOI: 10.1126/science.aas9129 Document Type: Article |
Times cited : (803)
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References (16)
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