Evidence map›Paper›PMID 19470237›Full record

ReviewBMB reports2009

Cell-intrinsic signals that regulate adult neurogenesis in vivo: insights from inducible approaches.

Madeleine A Johnson, Jessica L Ables, Amelia J Eisch

Open access · goldAbstract readReview
In one paragraph

Review in BMB reports, 2009. 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
3.9field-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

31 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  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

3 authors at 1 institution in 1 country.

Madeleine A JohnsonDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, 75390-9070, USA.
Jessica L Ables
Amelia J Eisch
The University of Texas Southwestern Medical Center · US

Funding

Basic Science Training Program in Drug Abuse ResearchT32DA007290 · NIDA · YALE UNIVERSITY · PI SELF, DAVID W · 1992 to 2017
$6.7M
Regulation of adult neurogenesis by opiatesR01DA016765 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI EISCH, AMELIA J · 2004 to 2013
$4.0M
Basic Science Training Program in the Neurobiology of Mental IllnessT32MH076690 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TAMMINGA, CAROL A · 2007 to 2017
$2.3M
New Horizons in Adult NeurogenesisK02DA023555 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI EISCH, AMELIA J · 2007 to 2017
$1.1M
Cdk5 and adult hippocampal neurogenesisR21DA023701 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI EISCH, AMELIA J · 2008 to 2009
$432k
NIDA NIH HHS DA016765NIDA NIH HHS DA023555NIDA NIH HHS DA023701NIDA NIH HHS K02 DA023555NIDA NIH HHS R01 DA016765NIDA NIH HHS R21 DA023701NIDA NIH HHS T32 DA007290NIDA NIH HHS T32-DA7290NIMH NIH HHS T32 MH076690NIMH NIH HHS T32-MH076690
6 · The paper itself

Abstract

The process by which adult neural stem cells generate new and functionally integrated neurons in the adult mammalian brain has been intensely studied, but much more remains to be discovered. It is known that neural progenitors progress through distinct stages to become mature neurons, and this progression is tightly controlled by cell-cell interactions and signals in the neurogenic niche. However, less is known about the cell-intrinsic signaling required for proper progression through stages of adult neurogenesis. Techniques have recently been developed to manipulate genes specifically in adult neural stem cells and progenitors in vivo, such as the use of inducible transgenic mice and viral-mediated gene transduction. A critical mass of publications utilizing these techniques has been reached, making it timely to review which molecules are now known to play a cell-intrinsic role in regulating adult neurogenesis in vivo. By drawing attention to these isolated molecules (e.g. Notch), we hope to stimulate a broad effort to understand the complex and compelling cascades of intrinsic signaling molecules important to adult neurogenesis. Understanding this process opens the possibility of understanding brain functions subserved by neurogenesis, such as memory, and also of harnessing neural stem cells for repair of the diseased and injured brain.

Indexed as

Adult Stem CellsAnimalsCyclic AMP Response Element-Binding ProteinCyclin-Dependent Kinase 5Gene Transfer TechniquesMiceMice, TransgenicNerve Tissue ProteinsNeurogenesisNeuronsReceptors, GABAReceptors, GlutamateReceptors, Nerve Growth FactorReceptors, NotchSignal TransductionWnt ProteinsCyclic AMP Response Element-Binding ProteinCyclin-Dependent Kinase 5DISC1 protein, humanNerve Tissue ProteinsReceptors, GABAReceptors, GlutamateReceptors, Nerve Growth FactorReceptors, NotchWnt Proteins

Identifiers

PMID19470237
PMCPMC3601036
OpenAlexW2047007525

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.