Evidence map›Paper›PMID 30735127›Full record

ArticleeLife2019

Specification of diverse cell types during early neurogenesis of the mouse cerebellum.

John W Wizeman, Qiuxia Guo, Elliott M Wilion, James Yh Li

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing 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

63 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Transcriptomic Analysis ofBrain sciences · 2025
    Article
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  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

3 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

4 authors.

John W Wizeman *Department of Genetics and Genome Sciences, School of Medicine, University of Connecticut, Farmington, United States.
Qiuxia Guo *Department of Genetics and Genome Sciences, School of Medicine, University of Connecticut, Farmington, United States.
Elliott M WilionUniversity of Connecticut, Storrs, United States.
James Yh LiDepartment of Genetics and Genome Sciences, School of Medicine, University of Connecticut, Farmington, United States.ORCID 0000-0002-9231-2698

Funding

MOLECULAR REGULATION OF LINEAGE SPECIFICATION OF THE MOUSE CEREBELLUMR01NS106844 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LI, JAMES Y.H · 2018 to 2022
$2.1M
NIH Office of the Director R01NS106844NINDS NIH HHS R01 NS106844University of Connecticut Health Research Program
6 · The paper itself

Abstract

We applied single-cell RNA sequencing to profile genome-wide gene expression in about 9400 individual cerebellar cells from the mouse embryo at embryonic day 13.5. Reiterative clustering identified the major cerebellar cell types and subpopulations of different lineages. Through pseudotemporal ordering to reconstruct developmental trajectories, we identified novel transcriptional programs controlling cell fate specification of populations arising from the ventricular zone and the rhombic lip, two distinct germinal zones of the embryonic cerebellum. Together, our data revealed cell-specific markers for studying the cerebellum, gene-expression cascades underlying cell fate specification, and a number of previously unknown subpopulations that may play an integral role in the formation and function of the cerebellum. Our findings will facilitate new discovery by providing insights into the molecular and cell type diversity in the developing cerebellum.

Indexed as

AnimalsCell DifferentiationCell LineageCerebellumEmbryo, MammalianEmbryonic DevelopmentGene Expression Regulation, DevelopmentalMiceNeurogenesisNeuronsSequence Analysis, RNASingle-Cell AnalysisTranscription FactorsTranscription Factorscell fate specificationcerebellar nucleidevelopmental biologymouseneural progenitorsorganizerPurkinje neuronssingle-cell transcriptomics

Identifiers

PMID30735127
PMCPMC6382353

What OpenQuestion holds

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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.