Evidence map›Paper›PMID 25191280›Full record

ReviewFrontiers in psychiatry2014

Role of the axonal initial segment in psychiatric disorders: function, dysfunction, and intervention.

Wei-Chun Jim Hsu, Carol Lynn Nilsson, Fernanda Laezza

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. JAK2 regulates Nav1.6 channel function via FGF14Biochimica et biophysica acta. Molecular cell research · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Imaging of the Axon Initial Segment.Current protocols in neuroscience · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The Axon Initial Segment: An Updated Viewpoint.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Wei-Chun Jim HsuDepartment of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Graduate Program in Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; M.D.-Ph.D. Combined Degree Program, The University of Texas Medical Branch at Galveston , Galveston, TX , USA.
Carol Lynn NilssonDepartment of Pharmacology and Toxicology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Sealy Center for Molecular Medicine, The University of Texas Medical Branch at Galveston , Galveston, TX , USA.
Fernanda LaezzaDepartment of Pharmacology and Toxicology, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Center for Addiction Research, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Center for Biomedical Engineering, The University of Texas Medical Branch at Galveston , Galveston, TX , USA ; Mitchell Center for Neurodegenerative Diseases, The University of Texas Medical Branch at Galveston , Galveston, TX , USA.
The University of Texas Medical Branch at Galveston · US

Funding

Validation of FGF14 as a New Molecular Target of GSK3R01MH095995 · NIMH · UNIVERSITY OF TEXAS MED BR GALVESTON · PI LAEZZA, FERNANDA · 2012 to 2016
$1.9M
NIMH NIH HHS R01 MH095995
6 · The paper itself

Abstract

The progress of developing effective interventions against psychiatric disorders has been limited due to a lack of understanding of the underlying cellular and functional mechanisms. Recent research findings focused on exploring novel causes of psychiatric disorders have highlighted the importance of the axonal initial segment (AIS), a highly specialized neuronal structure critical for spike initiation of the action potential. In particular, the role of voltage-gated sodium channels, and their interactions with other protein partners in a tightly regulated macromolecular complex has been emphasized as a key component in the regulation of neuronal excitability. Deficits and excesses of excitability have been linked to the pathogenesis of brain disorders. Identification of the factors and regulatory pathways involved in proper AIS function, or its disruption, can lead to the development of novel interventions that target these mechanistic interactions, increasing treatment efficacy while reducing deleterious off-target effects for psychiatric disorders.

Indexed as

axonal initial segmentneuronal excitabilityneuroplasticitypsychiatric disorderRDoCsignaling pathways

Identifiers

PMID25191280
PMCPMC4139700
OpenAlexW2011808913

What OpenQuestion holds

Textmetadata
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.