Saturation editing of genomic regions by multiplex homology-directed repair.

Nature

Volumn 513, Issue 7516, 2014, Pages 120-123

  Findlay, Gregory M ^a   Boyle, Evan A ^a   Hause, Ronald J ^a   Klein, Jason C ^a   Shendure, Jay ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CRISPR ASSOCIATED PROTEIN; LARIAT DEBRANCHING ENZYME; RNA POLYMERASE;

ARTICLE; CELL LINE; CLUSTERED REGULARLY INTERSPACED SHORT PALINDROMIC REPEAT; CRISPR CAS SYSTEM; DNA TEMPLATE; ESSENTIAL GENE; EXON; GENETICS; GENOMICS; HUMAN; METABOLISM; METHODOLOGY; MOLECULAR GENETICS; MUTAGENESIS; NONSENSE MEDIATED MRNA DECAY; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; POINT MUTATION; RECOMBINATION REPAIR; REGULATORY SEQUENCE; RNA SPLICING; TUMOR SUPPRESSOR GENE;

CELL LINE; CLUSTERED REGULARLY INTERSPACED SHORT PALINDROMIC REPEATS; CONSERVED SEQUENCE; CRISPR-ASSOCIATED PROTEINS; CRISPR-CAS SYSTEMS; EXONS; GENES, BRCA1; GENES, ESSENTIAL; GENOMICS; HUMANS; MOLECULAR SEQUENCE ANNOTATION; MUTAGENESIS; NONSENSE MEDIATED MRNA DECAY; OPEN READING FRAMES; POINT MUTATION; RECOMBINATIONAL DNA REPAIR; REGULATORY SEQUENCES, NUCLEIC ACID; RNA NUCLEOTIDYLTRANSFERASES; RNA SPLICING; TEMPLATES, GENETIC;

EID: 84907257107     PISSN: None     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature13695     Document Type: Article

References (0)