Evidence map›Paper›PMID 21800304›Full record

ArticleThe Journal of comparative neurology2011

Nuclear factor one X regulates the development of multiple cellular populations in the postnatal cerebellum.

Michael Piper, Lachlan Harris, Guy Barry, Yee Hsieh Evelyn Heng, Celine Plachez, Richard M Gronostajski, Linda J Richards

Abstract readComparative Study
In one paragraph

Article in The Journal of comparative neurology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Hydrocephalus inCells · 2022
    Article
  8. Temporarily Epigenetic Repression in Bergmann Glia Regulates the Migration of Granule Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. miR-210 promotes progression of endometrial carcinoma by regulating the expression of NFIX.International journal of clinical and experimental pathology · 2018
    Article
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 2 countries.

Michael PiperSchool of Biomedical Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia. m.piper@uq.edu.au
Lachlan Harris
Guy Barry
Yee Hsieh Evelyn Heng
Celine Plachez
Richard M Gronostajski
Linda J Richards
University of Queensland · AUUniversity at Buffalo, State University of New York · USUniversity of Maryland, Baltimore · US

Funding

Roles of NFI Genes in Mouse Lung DevelopmentR01HL080624 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI GRONOSTAJSKI, RICHARD M · 2007 to 2011
$2.0M
NHLBI NIH HHS HL080624NHLBI NIH HHS R01 HL080624
6 · The paper itself

Abstract

Development of the cerebellum involves the coordinated proliferation, differentiation, maturation, and integration of cells from multiple neuronal and glial lineages. In rodent models, much of this occurs in the early postnatal period. However, our understanding of the molecular mechanisms that regulate this phase of cerebellar development remains incomplete. Here, we address the role of the transcription factor nuclear factor one X (NFIX), in postnatal development of the cerebellum. NFIX is expressed by progenitor cells within the external granular layer and by cerebellar granule neurons within the internal granule layer. Using NFIX⁻/⁻ mice, we demonstrate that the development of cerebellar granule neurons and Purkinje cells within the postnatal cerebellum is delayed in the absence of this transcription factor. Furthermore, the differentiation of mature glia within the cerebellum, such as Bergmann glia, is also significantly delayed in the absence of NFIX. Collectively, the expression pattern of NFIX, coupled with the delays in the differentiation of multiple cell populations of the developing cerebellum in NFIX⁻/⁻ mice, suggest a central role for NFIX in the regulation of cerebellar development, highlighting the importance of this gene for the maturation of this key structure.

Indexed as

AnimalsAnimals, NewbornCerebellumCytoplasmic GranulesFemaleMaleMiceMice, Inbred C57BLMice, KnockoutNeurogenesisNFI Transcription FactorsStem CellsNFI Transcription FactorsNfix protein, mouse

Identifiers

PMID21800304
PMCPMC4032092
OpenAlexW2008713605

What OpenQuestion holds

Textmetadata
LicenceTDM
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.