Evidence map›Paper›PMID 34542410›Full record

ArticleeLife2021

Diverse inhibitory projections from the cerebellar interposed nucleus.

Elena N Judd, Samantha M Lewis, Abigail L Person

Abstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
–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

52 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Brain-wide mapping of developmental trajectories of cerebellar efferent projections.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Cerebellar control of targeted tongue movements.The Journal of physiology · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Behavioral decline in Shank3Molecular autism · 2024
    Article
  17. Characterization of direct Purkinje cell outputs to the brainstem.bioRxiv : the preprint server for biology · 2024
    Article
  18. Article
  19. Article
  20. A Virtual In Vivo Dissection and Analysis of Socioaffective Symptoms Related to Cerebellum-Midbrain Reward Circuitry in Humans.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    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

3 authors.

Elena N JuddDepartment of Physiology and Biophysics, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, United States.ORCID 0000-0001-8211-5140
Samantha M LewisDepartment of Physiology and Biophysics, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, United States.
Abigail L PersonDepartment of Physiology and Biophysics, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, United States.ORCID 0000-0001-9805-7600

Funding

University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
Circuit mechanisms of cerebellar control of reaching movementsR01NS114430 · NINDS · UNIVERSITY OF COLORADO DENVER · PI Jason M Christie, Abigail L Person · 2019 to 2026
$3.4M
NIDDK NIH HHS P30 DK116073NINDS NIH HHS P30 NS048154NINDS NIH HHS R01 NS114430
6 · The paper itself

Abstract

The cerebellum consists of parallel circuit modules that contribute to diverse behaviors, spanning motor to cognitive. Recent work employing cell-type-specific tracing has identified circumscribed output channels of the cerebellar nuclei (CbN) that could confer tight functional specificity. These studies have largely focused on excitatory projections of the CbN, however, leaving open the question of whether inhibitory neurons also constitute multiple output modules. We mapped output and input patterns to intersectionally restricted cell types of the interposed and adjacent interstitial nuclei in mice. In contrast to the widespread assumption of primarily excitatory outputs and restricted inferior olive-targeting inhibitory output, we found that inhibitory neurons from this region ramified widely within the brainstem, targeting both motor- and sensory-related nuclei, distinct from excitatory output targets. Despite differences in output targeting, monosynaptic rabies tracing revealed largely shared afferents to both cell classes. We discuss the potential novel functional roles for inhibitory outputs in the context of cerebellar theory.

Indexed as

AnimalsBrain MappingCell TrackingCerebellar NucleiFemaleMaleMiceMice, Mutant StrainsNeural PathwaysNeuronsSynapsescerebellumcircuitsinferior olivemouseneuroscience

Identifiers

PMID34542410
PMCPMC8483738

What OpenQuestion holds

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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.