Evidence map›Paper›PMID 20181580›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Origin and molecular specification of globus pallidus neurons.

Sandrina Nóbrega-Pereira, Diego Gelman, Giorgia Bartolini, Ramón Pla, Alessandra Pierani, Oscar Marín

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Arx revisited: involved in the development of GABAergic interneurons.Frontiers in cell and developmental biology · 2025
    Review
  7. Article
  8. Neuronal PAS domain 1 identifies a major subpopulation of wakefulness-promoting GABAergic neurons in the basal forebrain.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Evo-devo applied to sleep research: an approach whose time has come.Sleep advances : a journal of the Sleep Research Society · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Bilirubin Encephalopathy.Current neurology and neuroscience reports · 2022
    Review
  18. Single cell enhancer activity distinguishes GABAergic and cholinergic lineages in embryonic mouse basal ganglia.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Refocusing neuroscience: moving away from mental categories and towards complex behaviours.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  20. Article

20 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 3 countries.

Sandrina Nóbrega-PereiraInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas y Universidad Miguel Hernández, Sant Joan d'Alacant, Spain.
Diego Gelman
Giorgia Bartolini
Ramón Pla
Alessandra Pierani
Oscar Marín
Instituto de Neurociencias · ESConsejo Superior de Investigaciones Científicas · ESInstitut Jacques Monod · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanisms controlling the assembly of brain nuclei are poorly understood. In the forebrain, it is typically assumed that the formation of nuclei follows a similar sequence of events that in the cortex. In this structure, projection neurons are generated sequentially from common progenitor cells and migrate radially to reach their final destination, whereas interneurons are generated remotely and arrive to the cortex through tangential migration. Using the globus pallidus as a model to study the formation of forebrain nuclei, we found that the development of this basal ganglia structure involves the generation of several distinct classes of projection neurons from relatively distant progenitor pools, which then assemble together through tangential migration. Our results thus suggest that tangential migration in the forebrain is not limited to interneurons, as previously thought, but also involves projection neurons and reveal that the assembly of forebrain nuclei is more complex than previously anticipated.

Indexed as

AcetylcholineAnimalsBasic Helix-Loop-Helix ProteinsBiomarkersCell DifferentiationCell MovementCholine O-AcetyltransferaseDNA-Binding Proteinsgamma-Aminobutyric AcidGene Expression Regulation, DevelopmentalGlobus PallidusMiceMice, KnockoutMice, TransgenicNerve Tissue ProteinsNeural PathwaysAcetylcholineBasic Helix-Loop-Helix ProteinsBiomarkersCholine O-AcetyltransferaseDNA-Binding ProteinsEtv1 protein, mousegamma-Aminobutyric AcidNerve Tissue ProteinsNeuN protein, mouseNpas1 protein, mouseNuclear ProteinsParvalbuminsThyroid Nuclear Factor 1Transcription Factors

Identifiers

PMID20181580
PMCPMC6633933
OpenAlexW2093983408

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.