Evidence map›Paper›PMID 31488565›Full record

ArticleDevelopment (Cambridge, England)2019

CD40 forward signalling is a physiological regulator of early sensory axon growth.

Laura Howard, Thomas G McWilliams, Sean Wyatt, Alun M Davies

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Genes in Axonal Regeneration.Molecular neurobiology · 2024
    Review
  2. CD40-CD40L in Neurological Disease.International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. How CD40L reverse signaling regulates axon and dendrite growth.Cellular and molecular life sciences : CMLS · 2021
    Article
  7. Article
  8. 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

4 authors at 1 institution in 1 country.

Laura HowardSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AT, UK.
Thomas G McWilliamsSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AT, UK.
Sean WyattSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AT, UK.
Alun M DaviesSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AT, UK daviesalun@cf.ac.uk.ORCID 0000-0001-5841-8176
Cardiff University · GB

Funding

Wellcome Trust 103852
6 · The paper itself

Abstract

Multiple members of the tumour necrosis factor superfamily (TNFSF) regulate the growth and branching of neural processes late in development, when neurons are establishing and refining connections. Here, we present the first evidence that a TNFSF member acts much earlier in development, when axons are growing to their targets. CD40L transiently enhanced axon growth from embryonic mouse DRG neurons cultured at this early stage. Early spinal nerves of embryos lacking the CD40L receptor (

Indexed as

Signal TransductionAnimalsAutocrine CommunicationAxonsCD40 AntigensCD40 LigandCell SurvivalEmbryo, MammalianGanglia, SpinalGene DeletionGene Expression Regulation, DevelopmentalMice, Inbred C57BLNerve Growth FactorsRNA, MessengerSensory Receptor CellsSpinal NervesCD40 AntigensCD40 LigandNerve Growth FactorsRNA, MessengerCD40CD40LMouseSensory axonsTissue innervationTNF superfamily

Identifiers

PMID31488565
PMCPMC6765180
OpenAlexW2971446937

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.