Evidence map›Paper›PMID 19136970›Full record

ArticleNature neuroscience2009

The tumor suppressor Pml regulates cell fate in the developing neocortex.

Tarik Regad, Cristian Bellodi, Pierluigi Nicotera, Paolo Salomoni

Abstract read
PubMed Publisher
In one paragraph

Article in Nature neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

71 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
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  8. Nuclear Architecture in the Nervous System.Results and problems in cell differentiation · 2022
    Review
  9. Article
  10. PML Differentially Regulates Growth and Invasion in Brain Cancer.International journal of molecular sciences · 2021
    Article
  11. Article
  12. Article
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  15. Review
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11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Tarik RegadMedicial Research Council Toxicology Unit, University of Leicester, Box 138 Lancaster Road, Leicester LE1 7JL, UK.
Cristian Bellodi
Pierluigi Nicotera
Paolo Salomoni
University of Leicester · GBLeicester City Council · GB

Funding

Medical Research Council MC_U132670601
6 · The paper itself

Abstract

The control of cell fate in neural progenitor cells is critical for nervous system development. Nevertheless, the processes involved are only partially known. We found that the expression of the tumor suppressor Pml was restricted to neural progenitor cells (NPCs) in the developing neocortex of the mouse. Notably, in Pml(-/-) cortices, the overall number of proliferating NPCs was increased and transition between the two major progenitor types, radial glial cells and basal progenitors, was impaired. This in turn resulted in reduced differentiation and an overall decrease in the thickness of the cortex wall. In NPCs, Pml regulated the subcellular distribution of the retinoblastoma protein (pRb) and the protein phosphatase 1alpha, triggering pRb dephosphorylation. Together, these findings reveal an unexpected role of Pml in controlling the function of NPCs in the CNS.

Indexed as

NeocortexAnimalsCell DifferentiationCell DivisionCells, CulturedFemaleGene Expression Regulation, DevelopmentalMaleMiceMice, Mutant StrainsNeurogliaNeuronsNuclear ProteinsOrgan SizePhosphorylationPregnancyNuclear ProteinsPml protein, mousePromyelocytic Leukemia ProteinProtein Phosphatase 1Retinoblastoma ProteinTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID19136970
OpenAlexW2056216914

What OpenQuestion holds

Textmetadata
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.