Evidence map›Paper›PMID 31147612›Full record

ReviewNature reviews. Molecular cell biology2019

The next generation of CRISPR-Cas technologies and applications.

Adrian Pickar-Oliver, Charles A Gersbach

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 720 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
720citing papers in PubMed, 2 pooled it
65.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

720 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,458 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. CRISPR/Cas Systems: Biological Basis and Genome Editing Applications.Methods in molecular biology (Clifton, N.J.) · 2027
    Review
  4. CRISPR/Cas9-based nanodelivery systems for precision gene editing in neuroinflammation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Bacterial immune systems.Antonie van Leeuwenhoek · 2026
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

660 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Adrian Pickar-OliverDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Charles A GersbachDepartment of Biomedical Engineering, Duke University, Durham, NC, USA. charles.gersbach@duke.edu.ORCID http://orcid.org/0000-0003-1478-4013
Duke University · US

Funding

Decoding and Reprogramming the Corticosteroid Transcriptional Regulatory NetworkU01HG007900 · NHGRI · DUKE UNIVERSITY · PI REDDY, TIMOTHY E · 2015 to 2017
$5.9M
Regulatory Mechanisms of CD4+ T Cell DifferentiationUM1HG009428 · NHGRI · DUKE UNIVERSITY · PI CIOFANI, MARIA, CRAWFORD, GREGORY E · 2017 to 2021
$4.6M
Engineering Targeted Epigenetic Modifiers for Precise Control of Gene RegulationR01DA036865 · NIDA · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, GERSBACH, CHARLES A. · 2013 to 2017
$2.6M
Systemic Inflammation in Microphysiological Models of Muscle and Vascular DiseaseUG3TR002142 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2017 to 2018
$2.1M
CRISPR/Cas9-Based Gene Editing for the Correction of Duchenne Muscular DystrophyR01AR069085 · NIAMS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2016 to 2020
$1.7M
Tissue Procurement and Analysis CoreP30AR066527 · NIAMS · DUKE UNIVERSITY · PI HALL, RUSSELL P. · 2014 to 2015
$1.3M
In Vivo Epigenome Editing with CRISPR-Based Histone Acetyltransferase TransgenicR33DA041878 · NIDA · DUKE UNIVERSITY · PI GERSBACH, CHARLES A., WEST, ANNE ELIZABETH · 2018 to 2020
$1.1M
Enhancing Neuronal Reprogramming with Epigenome EditingR21NS103007 · NINDS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2018 to 2019
$427k
A Platform Technology for High-Throughput Screening of Gene Regulatory ElementsR41GM119914 · NIGMS · ELEMENT GENOMICS, INC. · PI CRAWFORD, GREGORY E, GERSBACH, CHARLES A. · 2016 to 2016
$225k
Reprogrammed T Cells to prevent graft versus host diseaseR41AI136755 · NIAID · ELEMENT GENOMICS, INC. · PI BELLUCCI, JOSEPH J · 2018 to 2018
$222k
NCATS NIH HHS UG3 TR002142NHGRI NIH HHS U01 HG007900NHGRI NIH HHS UM1 HG009428NIAID NIH HHS R41 AI136755NIAMS NIH HHS P30 AR066527NIAMS NIH HHS R01 AR069085NIDA NIH HHS R01 DA036865NIDA NIH HHS R33 DA041878NIGMS NIH HHS R41 GM119914NINDS NIH HHS R21 NS103007
6 · The paper itself

Abstract

The prokaryote-derived CRISPR-Cas genome editing systems have transformed our ability to manipulate, detect, image and annotate specific DNA and RNA sequences in living cells of diverse species. The ease of use and robustness of this technology have revolutionized genome editing for research ranging from fundamental science to translational medicine. Initial successes have inspired efforts to discover new systems for targeting and manipulating nucleic acids, including those from Cas9, Cas12, Cascade and Cas13 orthologues. Genome editing by CRISPR-Cas can utilize non-homologous end joining and homology-directed repair for DNA repair, as well as single-base editing enzymes. In addition to targeting DNA, CRISPR-Cas-based RNA-targeting tools are being developed for research, medicine and diagnostics. Nuclease-inactive and RNA-targeting Cas proteins have been fused to a plethora of effector proteins to regulate gene expression, epigenetic modifications and chromatin interactions. Collectively, the new advances are considerably improving our understanding of biological processes and are propelling CRISPR-Cas-based tools towards clinical use in gene and cell therapies.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsEndonucleasesGene EditingGenetic TherapyRNA, Guide, CRISPR-Cas SystemsAnimalsHumansEndonucleasesRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID31147612
PMCPMC7079207
OpenAlexW2947777875

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.