Evidence map›Paper›PMID 30542270›Full record

ArticleFrontiers in cellular neuroscience2018

Protein Kinase C Inhibition Mediates Neuroblast Enrichment in Mechanical Brain Injuries.

Francisco García-Bernal, Noelia Geribaldi-Doldán, Samuel Domínguez-García, Manuel Carrasco, Maribel Murillo-Carretero, Antonio Delgado-Ariza, Mónica Díez-Salguero, Cristina Verástegui, Carmen Castro

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  6. Review
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  9. Review
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  11. Effects of classical PKC activation on hippocampal neurogenesis and cognitive performance: mechanism of action.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Protein Kinase C: Targets to Regenerate Brain Injuries?Frontiers in cell and developmental biology · 2019
    Article
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

9 authors at 3 institutions in 1 country.

Francisco García-BernalÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Noelia Geribaldi-DoldánÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Samuel Domínguez-GarcíaÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Manuel CarrascoÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Maribel Murillo-CarreteroÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Antonio Delgado-ArizaÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Mónica Díez-SalgueroÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Cristina VerásteguiÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Carmen CastroÁrea de Fisiología, Facultad de Medicina, Universidad de Cádiz, Cádiz, Spain.
Instituto de Investigación Biomédica de A Coruña · ESUniversidad de Cádiz · ESBiomedical Research and Innovation Institute of Cadiz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain injuries of different etiologies lead to irreversible neuronal loss and persisting neuronal deficits. New therapeutic strategies are emerging to compensate neuronal damage upon brain injury. Some of these strategies focus on enhancing endogenous generation of neurons from neural stem cells (NSCs) to substitute the dying neurons. However, the capacity of the injured brain to produce new neurons is limited, especially in cases of extensive injury. This reduced neurogenesis is a consequence of the effect of signaling molecules released in response to inflammation, which act on intracellular pathways, favoring gliogenesis and preventing recruitment of neuroblasts from neurogenic regions. Protein kinase C (PKC) is a family of intracellular kinases involved in several of these gliogenic signaling pathways. The aim of this study was to analyze the role of PKC isozymes in the generation of neurons from neural progenitor cells (NPCs)

Indexed as

brain injuriesneuroblastsneurogenesisneuronal differentiationPKC

Identifiers

PMID30542270
PMCPMC6277931
OpenAlexW2902820951

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.