Evidence map›Paper›PMID 28729824›Full record

ReviewFrontiers in cellular neuroscience2017

Mouse Models of

Ranjan Batra, Chris W Lee

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Arrayed dual-gRNA CRISPR screening platform forMolecular therapy. Advances · 2026
    Article
  2. Drug repurposing in amyotrophic lateral sclerosis (ALS).Expert opinion on drug discovery · 2025
    Review
  3. Article
  4. Review
  5. Gut microbiota immune cross-talk in amyotrophic lateral sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. The progress inSmall GTPases · 2022
    Review
  15. Gene therapy for ALS: A review.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  16. Review
  17. Article
  18. Review
  19. Inducible expression of humanDisease models & mechanisms · 2021
    Article
  20. Review
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 2 institutions in 1 country.

Ranjan BatraDepartment of Cellular and Molecular Medicine, University of California, San Diego, La JollaCA, United States.
Chris W LeeAtlantic Health System, MorristownNJ, United States.
Atlantic Health System · USUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of hexanucleotide repeat expansion (HRE) in the first intron of the human

Indexed as

adeno-associated viral vectoramyotrophic lateral sclerosisbacterial artificial chromosomeC9orf72frontotemporal dementiamicrosatellite repeat expansionmouse modelRNA toxicity

Identifiers

PMID28729824
PMCPMC5498553
OpenAlexW2727124836

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.