review·Cell·Apr 1, 2020GREEN OA

CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors

DWDan WangCorresponding authorFZFeng ZhangGGGuangping Gao

University of Massachusetts Chan Medical School · Broad Institute · +3 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

No abstract available for this paper.

Citation impact

515
total citations
FWCI
23.67
Percentile
100%
References
178
Citations per year

Authors

3
  • DW
    Dan WangCorresponding

    University of Massachusetts Chan Medical School

  • FZ
    Feng Zhang

    Broad Institute, Howard Hughes Medical Institute, McGovern Institute for Brain Research, Massachusetts Institute of Technology

  • GG
    Guangping Gao

    University of Massachusetts Chan Medical School

Topics & keywords

Topics
  • Primary topicCRISPR and Genetic Engineering100%
  • Innovation and Socioeconomic Development99%
  • Virus-based gene therapy research93%
Keywords
  • Biology
  • CRISPR
  • Genome editing
  • Computational biology
  • Genome
  • Vector (molecular biology)
  • In vivo
  • Genetics
No related works found for this paper.

Funding

  • HH
    Howard Hughes Medical Institute
  • CF
    Cystic Fibrosis Foundation
  • MP
    Michelson Prize and Grants
  • MI
    Massachusetts Institute of Technology
  • PH
    Pitt Hopkins Research Foundation
  • GH
    G. Harold and Leila Y. Mathers Foundation
  • GS
    Grace Science Foundation
  • EM
    Edward Mallinckrodt, Jr. Foundation
  • NI
    National Institutes of Health