Evidence map›Paper›PMID 38727583›Full record

ArticleeLife2024

Txnip deletions and missense alleles prolong the survival of cones in a retinitis pigmentosa mouse model.

Yunlu Xue, Yimin Zhou, Constance L Cepko

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Yunlu XueDepartments of Genetics and Ophthalmology, Blavatnik Institute, Harvard Medical School, Boston, United States.ORCID https://orcid.org/0000-0002-2088-9826
Yimin ZhouLingang Laboratory, Shanghai, China.
Constance L CepkoDepartments of Genetics and Ophthalmology, Blavatnik Institute, Harvard Medical School, Boston, United States.ORCID https://orcid.org/0000-0002-9945-6387

Funding

Investigation of the Mechanisms of Cone Degeneration in Retinitis PigmentosaK99EY030951 · NEI · HARVARD MEDICAL SCHOOL · PI XUE, YUNLU · 2020 to 2022
$242k
NEI NIH HHS K99 EY030951NEI NIH HHS K99EY030951
6 · The paper itself

Abstract

Retinitis pigmentosa (RP) is an inherited retinal disease in which there is a loss of cone-mediated daylight vision. As there are >100 disease genes, our goal is to preserve cone vision in a disease gene-agnostic manner. Previously we showed that overexpressing TXNIP, an α-arrestin protein, prolonged cone vision in RP mouse models, using an AAV to express it only in cones. Here, we expressed different alleles of

Indexed as

Retinal Cone Photoreceptor CellsRetinitis PigmentosaThioredoxinsAllelesAnimalsCarrier ProteinsCell SurvivalDisease Models, AnimalGene DeletionMiceMutation, MissenseRetinal Pigment EpitheliumCarrier ProteinsThioredoxinsTxnip protein, mouseHSP90AB1medicinemouseneuroscienceretinaTXNIP

Identifiers

PMID38727583
PMCPMC11087050

What OpenQuestion holds

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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.