Evidence map›Paper›PMID 25410355›Full record

ReviewProgress in brain research2014

ECM receptors in neuronal structure, synaptic plasticity, and behavior.

Meghan E Kerrisk, Lorenzo A Cingolani, Anthony J Koleske

Open access · greenAbstract readReview
In one paragraph

Review in Progress in brain research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 4% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Blocking the mCellular & molecular immunology · 2026
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  6. Connecting the Dots: AMOG/βInternational journal of molecular sciences · 2025
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  9. Article
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  11. Article
  12. Article
  13. RANBP17 Overexpression Restores Nucleocytoplasmic Transport and Ameliorates Neurodevelopment in Induced DYT1 Dystonia Motor Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Myelination dictates axonal viscoelasticity.The European journal of neuroscience · 2023
    Article
  20. CRISPR-mediated activation of autism geneMolecular therapy. Nucleic acids · 2022
    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 2 institutions in 2 countries.

Meghan E KerriskDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.
Lorenzo A CingolaniDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genoa, Italy.
Anthony J KoleskeDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA; Department of Neurobiology, Yale University, New Haven, CT, USA; Interdepartmental Neuroscience Program, Yale University, New Haven, CT, USA; Program in Cellular Neuroscience, Neurodegeneration, and Repair, Yale University, New Haven, CT, USA. Electronic address: anthony.koleske@yale.edu.
Yale University · USItalian Institute of Technology · IT

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
Roles of Abl and Arg Neuronal DevelopmentR01NS039475 · NINDS · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2000 to 2012
$4.3M
Supplement to Regulation of invadopodia formation in breast cancer cellsR01CA133346 · NCI · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2009 to 2016
$2.3M
The mechanism of Arg kinase activation by integrin B1R01GM100411 · NIGMS · YALE UNIVERSITY · PI BOGGON, TITUS JONATHON, KOLESKE, ANTHONY J · 2012 to 2015
$1.3M
NCI NIH HHS CA133346NCI NIH HHS R01 CA133346NIGMS NIH HHS GM100411NIGMS NIH HHS R01 GM100411NIGMS NIH HHS T32 GM007223NINDS NIH HHS NS39475NINDS NIH HHS R01 NS039475
6 · The paper itself

Abstract

During central nervous system development, extracellular matrix (ECM) receptors and their ligands play key roles as guidance molecules, informing neurons where and when to send axonal and dendritic projections, establish connections, and form synapses between pre- and postsynaptic cells. Once stable synapses are formed, many ECM receptors transition in function to control the maintenance of stable connections between neurons and regulate synaptic plasticity. These receptors bind to and are activated by ECM ligands. In turn, ECM receptor activation modulates downstream signaling cascades that control cytoskeletal dynamics and synaptic activity to regulate neuronal structure and function and thereby impact animal behavior. The activities of cell adhesion receptors that mediate interactions between pre- and postsynaptic partners are also strongly influenced by ECM composition. This chapter highlights a number of ECM receptors, their roles in the control of synapse structure and function, and the impact of these receptors on synaptic plasticity and animal behavior.

Indexed as

AnimalsBehaviorCentral Nervous SystemHumansNeuronal PlasticityNeuronsReceptors, Cell Surfaceextracellular matrix receptorReceptors, Cell Surfacecell adhesion receptorheparan sulfate proteoglycanintegrin receptorlipoprotein receptorL-type voltage-dependent calcium channeltetraspanin

Identifiers

PMID25410355
PMCPMC4640673
OpenAlexW2173821792

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.