Evidence map›Paper›PMID 41809907›Full record

ArticleData in brief2026

A time-resolved RNA-sequencing dataset of transcriptional responses in PC12 cells to NGF withdrawal and replenishment.

Peter Neufeld, Eliza Grlickova-Duzevik, Benjamin J Harrison

Abstract read
In one paragraph

Article in Data in brief, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Peter NeufeldDepartment of Biomedical Sciences, University of New England, Biddeford, ME 04005, USA.
Eliza Grlickova-DuzevikDepartment of Biomedical Sciences, University of New England, Biddeford, ME 04005, USA.
Benjamin J HarrisonDepartment of Biomedical Sciences, University of New England, Biddeford, ME 04005, USA.

Funding

Tissue resident macrophages in sensory ganglia: function and impact on nociceptionP20GM103643 · NIGMS · UNIVERSITY OF NEW ENGLAND · PI MENG, IAN D · 2012 to 2021
$20.9M
NIGMS NIH HHS P20 GM103643
6 · The paper itself

Abstract

Nerve Growth Factor (NGF) is a pleotropic extracellular signalling peptide with neurotrophic, cell differentiation, and cell survival functions. Binding of NGF ligand to tyrosine kinase receptors stimulates intracellular cascades to impact gene transcription. Transcriptional responses coordinate neurodevelopment, and regulate the sensitivity and excitability of populations of adult neurons. NGF is synthesized during inflammation, inducing plasticity of sensory neurons and contributing to chronic pain. PC12 cells, derived from rat pheochromocytoma, are a classical model of NGF responses, that differentiate upon NGF treatment into neuron-like cells, with neurites and growth cones dependent on continued exposure to NGF. This dataset comprises a time series from NGF-differentiated PC12 cells subject to NGF withdrawal and subsequent replenishment. These data serve as a resource for the community to elucidate NGF-dependent time-resolved gene transcription in peripheral neuron-like cells. RNA was extracted, sequenced, and mapped to the rat genome. QC measures and analysis of time-dependent gene expression changes validated by analysis of known marker genes show that this sequencing data is robust and contains thousands of transcriptional events for future study. These data are available in the sequence read archive (SRA) and serve as a valuable resource for the study of NGF-dependent transcription.

Indexed as

Gene expression profilingNerve growth factorPC12

Identifiers

PMID41809907
PMCPMC12969003

What OpenQuestion holds

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Registered trials

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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.