Evidence map›Paper›PMID 22811939›Full record

ReviewNeural plasticity2012

Pathological plasticity in fragile X syndrome.

Brandon S Martin, Molly M Huntsman

Abstract readReview
In one paragraph

Review in Neural plasticity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Astrocytes in fragile X syndrome.Frontiers in cellular neuroscience · 2023
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Synapse assembly and neurodevelopmental disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Homeostatic responses fail to correct defective amygdala inhibitory circuit maturation in fragile X syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  18. 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

2 authors.

Brandon S MartinCenter for Neuroscience Research, Children's National Medical Center, Washington, DC 20010, USA.
Molly M Huntsman

Funding

Testing the excitability of inhibitory neuronsR01NS053719 · NINDS · GEORGETOWN UNIVERSITY · PI HUNTSMAN, MOLLY-MAUREEN · 2007 to 2010
$1.1M
NINDS NIH HHS R01 NS053719NINDS NIH HHS R01NS053719
6 · The paper itself

Abstract

Deficits in neuronal plasticity are common hallmarks of many neurodevelopmental disorders. In the case of fragile-X syndrome (FXS), disruption in the function of a single gene, FMR1, results in a variety of neurological consequences directly related to problems with the development, maintenance, and capacity of plastic neuronal networks. In this paper, we discuss current research illustrating the mechanisms underlying plasticity deficits in FXS. These processes include synaptic, cell intrinsic, and homeostatic mechanisms both dependent on and independent of abnormal metabotropic glutamate receptor transmission. We place particular emphasis on how identified deficits may play a role in developmental critical periods to produce neuronal networks with permanently decreased capacity to dynamically respond to changes in activity central to learning, memory, and cognition in patients with FXS. Characterizing early developmental deficits in plasticity is fundamental to develop therapies that not only treat symptoms but also minimize the developmental pathology of the disease.

Indexed as

Adaptor Proteins, Signal TransducingFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHomeostasisHumansNerve NetNeuronal PlasticityReceptors, CannabinoidReceptors, GlutamateAdaptor Proteins, Signal TransducingCYFIP1 protein, humanFragile X Messenger Ribonucleoprotein 1Receptors, CannabinoidReceptors, Glutamate

Identifiers

PMID22811939
PMCPMC3395158

What OpenQuestion holds

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LicenceCC BY
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.