Evidence map›Paper›PMID 30737497›Full record

ArticleNature methods2019

In vivo RNA editing of point mutations via RNA-guided adenosine deaminases.

Dhruva Katrekar, Genghao Chen, Dario Meluzzi, Ashwin Ganesh, Atharv Worlikar, Yu-Ru Shih, Shyni Varghese, Prashant Mali

Open access · greenAbstract read
In one paragraph

Article in Nature methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed
9.3field-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

133 citing papers in PubMed, 211 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Evolution of Engineered ADAR-Based RNA Editing Systems.International journal of molecular sciences · 2026
    Review
  12. Article
  13. A Translational Roadmap for Neurological Nonsense Mutation Disorders.International journal of molecular sciences · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Regulatable In Vivo Gene Expression via Adaptamers.bioRxiv : the preprint server for biology · 2025
    Article
  18. Article
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Dhruva KatrekarDepartment of Bioengineering, University of California, San Diego, CA, USA.
Genghao ChenDepartment of Bioengineering, University of California, San Diego, CA, USA.
Dario MeluzziDepartment of Bioengineering, University of California, San Diego, CA, USA.ORCID http://orcid.org/0000-0001-5185-264X
Ashwin GaneshDepartment of Bioengineering, University of California, San Diego, CA, USA.
Atharv WorlikarDepartment of Bioengineering, University of California, San Diego, CA, USA.
Yu-Ru ShihDepartment of Bioengineering, University of California, San Diego, CA, USA.
Shyni VargheseDepartment of Bioengineering, University of California, San Diego, CA, USA.
Prashant MaliDepartment of Bioengineering, University of California, San Diego, CA, USA. pmali@ucsd.edu.ORCID http://orcid.org/0000-0002-3383-1287
University of California San Diego · USDuke University · US

Funding

Next-generation Functional Genetic Screening of Un-screenable TraitsR01HG009285 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MALI, PRASHANT, TAMAYO, PABLO · 2017 to 2020
$4.2M
Systematic mapping of genetic vulnerabilities in head and neck cancerR01CA222826 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MALI, PRASHANT · 2018 to 2022
$1.8M
Dissecting the interplay of gene regulatory networks and cellular niche on cell fate determinationR01GM123313 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MALI, PRASHANT · 2018 to 2021
$1.2M
See-ing the 4D Nucleome: Enhancer Cooperativity in Phase Separated StructuresK01DK119687 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MELUZZI, DARIO · 2018 to 2020
$356k
Enhancer networks and chromosomal architecture in ligand-regulated gene transcription programsF32DK112682 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MELUZZI, DARIO · 2016 to 2018
$106k
NCI NIH HHS R01 CA222826NHGRI NIH HHS R01 HG009285NIDDK NIH HHS F32 DK112682NIDDK NIH HHS K01 DK119687NIGMS NIH HHS R01 GM123313
6 · The paper itself

Abstract

We present in vivo sequence-specific RNA base editing via adenosine deaminases acting on RNA (ADAR) enzymes with associated ADAR guide RNAs (adRNAs). To achieve this, we systematically engineered adRNAs to harness ADARs, and comprehensively evaluated the specificity and activity of the toolsets in vitro and in vivo via two mouse models of human disease. We anticipate that this platform will enable tunable and reversible engineering of cellular RNAs for diverse applications.

Indexed as

Point MutationRNA EditingAdenosine DeaminaseAnimalsDisease Models, AnimalHEK293 CellsHigh-Throughput Nucleotide SequencingHumansMiceRNA, Guide, CRISPR-Cas SystemsRNA, MessengerRNA SplicingAdenosine DeaminaseRNA, Guide, CRISPR-Cas SystemsRNA, Messenger

Identifiers

PMID30737497
PMCPMC6395520
OpenAlexW2912112263

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.