Evidence map›Paper›PMID 29802307›Full record

ArticleScientific reports2018

TDP-43 induces p53-mediated cell death of cortical progenitors and immature neurons.

Miriam A Vogt, Zahra Ehsaei, Philip Knuckles, Adrian Higginbottom, Michaela S Helmbrecht, Tilo Kunath, Kevin Eggan, Luis A Williams, Pamela J Shaw, Wolfgang Wurst and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 57 citations in OpenAlex.

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  4. TDP-43: unveiling the hidden key to cellular fate decisions.Cell communication and signaling : CCS · 2025
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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

13 authors at 6 institutions in 4 countries.

Miriam A VogtDepartment of Biomedicine, University of Basel, Mattenstrasse 28, 4058, Basel, Switzerland.
Zahra EhsaeiDepartment of Biomedicine, University of Basel, Mattenstrasse 28, 4058, Basel, Switzerland.
Philip KnucklesFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058, Basel, Switzerland.
Adrian HigginbottomSheffield Institute for Translational Neuroscience (SITraN), University of Sheffield, 385A Glossop Road, Sheffield, S10 2HQ, UK.
Michaela S HelmbrechtHelmholtz Zentrum München, Ingolstädter Landstrasse 1, 85764, Neuherberg, Germany.
Tilo KunathMRC Centre for Regenerative Medicine, The University of Edinburgh, 5 Little France Drive, Edinburgh, EH16 4UU, UK.ORCID 0000-0002-8805-7356
Kevin EgganHarvard Stem Cell Institute, Harvard University, Howard Hughes Medical Institute, 7 Divinity Avenue, Cambridge, MA, 02138, USA.
Luis A WilliamsHarvard Stem Cell Institute, Harvard University, Howard Hughes Medical Institute, 7 Divinity Avenue, Cambridge, MA, 02138, USA.
Pamela J ShawSheffield Institute for Translational Neuroscience (SITraN), University of Sheffield, 385A Glossop Road, Sheffield, S10 2HQ, UK.
Wolfgang WurstHelmholtz Zentrum München, Ingolstädter Landstrasse 1, 85764, Neuherberg, Germany.
Thomas FlossHelmholtz Zentrum München, Ingolstädter Landstrasse 1, 85764, Neuherberg, Germany.
Andrea B HuberHelmholtz Zentrum München, Ingolstädter Landstrasse 1, 85764, Neuherberg, Germany.
Verdon TaylorDepartment of Biomedicine, University of Basel, Mattenstrasse 28, 4058, Basel, Switzerland. verdon.taylor@unibas.ch.ORCID 0000-0003-3497-5976
Helmholtz Zentrum München · DEUniversity of Basel · CHHoward Hughes Medical Institute · USUniversity of Sheffield · GBFriedrich Miescher Institute · CHMRC Centre for Regenerative Medicine · GB

Funding

Medical Research Council MR/J012831/1
6 · The paper itself

Abstract

TAR DNA-binding protein 43 (TDP-43) is a key player in neurodegenerative diseases including frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). Accumulation of TDP-43 is associated with neuronal death in the brain. How increased and disease-causing mutant forms of TDP-43 induce cell death remains unclear. Here we addressed the role of TDP-43 during neural development and show that reduced TDP-43 causes defects in neural stem/progenitor cell proliferation but not cell death. However, overexpression of wild type and TDP-43

Indexed as

ApoptosisAnimalsCell CycleCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsGene Expression RegulationHumansInduced Pluripotent Stem CellsMiceMutationNeural Stem CellsNeurogenesisNeuronsRNA, MessengerTumor Suppressor Protein p53Cdkn1a protein, mouseCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsRNA, MessengerTardbp protein, mouseTumor Suppressor Protein p53

Identifiers

PMID29802307
PMCPMC5970242
OpenAlexW2803422184

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.