Evidence map›Paper›PMID 15385616›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

The Tlx gene regulates the timing of neurogenesis in the cortex.

Kristine Roy, Kathleen Kuznicki, Qiang Wu, Zhuoxin Sun, Dagmar Bock, Gunther Schutz, Nancy Vranich, A Paula Monaghan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

74 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Dissecting Gene Regulatory Networks Governing Human Cortical Cell Fate.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. The Epigenome in Neurodevelopmental Disorders.Frontiers in neuroscience · 2021
    Review
  8. Article
  9. Article
  10. Nuclear receptors in neural stem/progenitor cell homeostasis.Cellular and molecular life sciences : CMLS · 2017
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

14 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

8 authors at 3 institutions in 2 countries.

Kristine RoyDepartment of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.
Kathleen Kuznicki
Qiang Wu
Zhuoxin Sun
Dagmar Bock
Gunther Schutz
Nancy Vranich
A Paula Monaghan
University of Pittsburgh · USGerman Cancer Research Center · DERutgers, The State University of New Jersey · US

Funding

MOLECULAR GENETIC ANALYSIS OF FOREBRAIN DEVELOPMENTR01MH060774 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MONAGHAN-NICHOLS, A PAULA · 2000 to 2008
$2.3M
NIMH NIH HHS 5R01MH060774NIMH NIH HHS R01 MH060774
6 · The paper itself

Abstract

The tailless (tlx) gene is a forebrain-restricted transcription factor. Tlx mutant animals exhibit a reduction in the size of the cerebral hemispheres and associated structures (Monaghan et al., 1997). Superficial cortical layers are specifically reduced, whereas deep layers are relatively unaltered (Land and Monaghan, 2003). To determine whether the adult laminar phenotype has a developmental etiology and whether it is associated with a change in proliferation/differentiation decisions, we examined the cell cycle and neurogenesis in the embryonic cortex. We found that there is a temporal and regional requirement for the Tlx protein in progenitor cells (PCs). Neurons prematurely differentiate at all rostrocaudal levels up to mid-neurogenesis in mutant animals. Heterozygote animals have an intermediate phenotype indicating there is a threshold requirement for Tlx in early cortical neurogenesis. Our studies indicate that PCs in the ventricular zone are sensitive to loss of Tlx in caudal regions only; however, PCs in the subventricular zone are altered at all rostrocaudal levels in tlx-deficient animals. Furthermore, we found that the cell cycle is shorter from embryonic day 9.5 in tlx-/- embryos. At mid-neurogenesis, the PC population becomes depleted, and late PCs have a longer cell cycle in tlx-deficient animals. Consequently, later generated structures, such as upper cortical layers, the dentate gyrus, and the olfactory bulbs, are severely reduced. These studies indicate that tlx is an essential intrinsic regulator in the decision to proliferate or differentiate in the developing forebrain.

Indexed as

AnimalsBromodeoxyuridineCell CountCell DifferentiationCerebral CortexGene DeletionHomozygoteImmunohistochemistryIn Situ HybridizationMiceMice, Inbred C57BLMice, KnockoutMice, Mutant StrainsNervous System MalformationsNeuronsReceptors, Cytoplasmic and NuclearBromodeoxyuridineNr2e1 protein, mouseReceptors, Cytoplasmic and Nuclear

Identifiers

PMID15385616
PMCPMC2740800
OpenAlexW2139452105

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.