Evidence map›Paper›PMID 37006469›Full record

ArticleFrontiers in cellular neuroscience2023

LPS-stimulated microglial cells promote ganglion cell death in organotypic cultures of quail embryo retina.

Ana Sierra-Martín, Julio Navascués, Veronika E Neubrand, M Rosario Sepúlveda, David Martín-Oliva, Miguel A Cuadros, José L Marín-Teva

Open access · goldFull text read
In one paragraph

Article in Frontiers in cellular neuroscience, 2023. 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
0.1field-weighted citation impact, top 55% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. Cell death by phagocytosis.Nature reviews. Immunology · 2024
    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

7 authors at 1 institution in 1 country.

Ana Sierra-MartínDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
Julio NavascuésDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
Veronika E NeubrandDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
M Rosario SepúlvedaDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
David Martín-OlivaDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
Miguel A CuadrosDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
José L Marín-TevaDepartment of Cell Biology, Faculty of Sciences, University of Granada, Granada, Spain.
Universidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During development microglia colonize the central nervous system (CNS) and play an important role in programmed cell death, not only because of their ability to remove dead cells by phagocytosis, but also because they can promote the death of neuronal and glial cells. To study this process, we used as experimental systems the developing

Indexed as

ganglion cell deathiNOSLPS-stimulationmicroglianitric oxideorganotypic culturesquailretina

Identifiers

PMID37006469
PMCPMC10050569
OpenAlexW4324373653

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read2
measurements read75
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.