Evidence map›Paper›PMID 17003522›Full record

ReviewMolecular neurobiology2006

Central nervous system functions of PAK protein family: from spine morphogenesis to mental retardation.

Bernadett Boda, Irina Nikonenko, Stefano Alberi, Dominique Muller

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. nArgBP2 regulates excitatory synapse formation by controlling dendritic spine morphology.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  7. Article
  8. Review
  9. PAK inactivation impairs social recognition in 3xTg-AD Mice without increasing brain deposition of tau and Aβ.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  10. Article
  11. Article
  12. Article
  13. Long-term potentiation-dependent spine enlargement requires synaptic Ca2+-permeable AMPA receptors recruited by CaM-kinase I.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  14. Review
  15. Article
  16. Evidence that long-term potentiation occurs within individual hippocampal synapses during learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  17. Article
  18. Changes in synaptic morphology accompany actin signaling during LTP.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  19. Review
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.

Bernadett BodaDepartment of Neuroscience, Centre Médical Universitaire, 1211 Geneva 4, Switzerland.
Irina Nikonenko
Stefano Alberi
Dominique Muller

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several of the genes currently known to be associated, when mutated, with mental retardation, code for molecules directly involved in Rho guanosine triphosphatase (GTPase) signaling. These include PAK3, a member of the PAK protein kinase family, which are important effectors of small GTPases. In many systems, PAK kinases play crucial roles regulating complex mechanisms such as cell migration, differentiation, or survival. Their precise functions in the central nervous system remain, however, unclear. Although their activity does not seem to be required for normal brain development, several recent studies point to a possible involvement in more subtle mechanisms such as neurite outgrowth, spine morphogenesis or synapse formation, and plasticity. This article reviews this information in the light of the current knowledge available on the molecular characteristics of the different members of this family and discuss the mechanisms through which they might contribute to cognitive functions.

Indexed as

AnimalsCentral Nervous SystemHumansNeuronsp21-Activated KinasesSignal Transductionp21-Activated Kinases

Identifiers

PMID17003522
OpenAlexW2002775724

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.