Evidence map›Paper›PMID 28170151›Full record

ReviewDevelopmental neurobiology2017

The electrical synapse: Molecular complexities at the gap and beyond.

Adam C Miller, Alberto E Pereda

Abstract readReview
In one paragraph

Review in Developmental neurobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
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  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
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  14. Article
  15. Review
  16. Article
  17. The Roles of Calmodulin and CaMKII in Cx36 Plasticity.International journal of molecular sciences · 2021
    Review
  18. Review
  19. Review
  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

2 authors.

Adam C MillerInstitute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon.ORCID 0000-0001-7519-3677
Alberto E PeredaDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York.

Funding

Plasticity of Electrical SynapsesR01DC011099 · NIDCD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Alberto E Pereda · 2010 to 2026
$7.0M
Control of Junctional Conductance at Auditory AfferentsR01DC003186 · NIDCD · YESHIVA UNIVERSITY · PI PEREDA, ALBERTO E · 2002 to 2006
$1.7M
In-vivo Modulation of Synapses by EndocannabinoidsR01NS052827 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PEREDA, ALBERTO E · 2006 to 2009
$1.1M
Molecular mechanisms of electrical synapse formation in vivoR00NS085035 · NINDS · UNIVERSITY OF OREGON · PI MILLER, ADAM C · 2016 to 2018
$747k
Generation of transgenic zebrafish to study electrical synaptic transmissionR21NS085772 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI PEREDA, ALBERTO E · 2013 to 2014
$469k
Control of Junctional Conductance at Auditory AfferentR56DC003186 · NIDCD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PEREDA, ALBERTO E · 2009 to 2009
$429k
Plasticity of Mammalian Electrical SynapsesR21NS055726 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PEREDA, ALBERTO E · 2007 to 2008
$399k
CONTROL OF JUNCTIONAL CONDUCTANCE AT AUDITORY AFFERENTSR29DC003186 · NIDCD · YESHIVA UNIVERSITY · PI PEREDA, ALBERTO E · 1997 to 2001
$238k
Molecular mechanisms of electrical synapse formation in vivoK99NS085035 · NINDS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MILLER, ADAM C · 2013 to 2014
$180k
NIDCD NIH HHS R01 DC003186NIDCD NIH HHS R01 DC011099NIDCD NIH HHS R29 DC003186NIDCD NIH HHS R56 DC003186NINDS NIH HHS K99 NS085035NINDS NIH HHS R00 NS085035NINDS NIH HHS R01 NS052827NINDS NIH HHS R21 NS055726NINDS NIH HHS R21 NS085772
6 · The paper itself

Abstract

Gap junctions underlie electrical synaptic transmission between neurons. Generally perceived as simple intercellular channels, "electrical synapses" have demonstrated to be more functionally sophisticated and structurally complex than initially anticipated. Electrical synapses represent an assembly of multiple molecules, consisting of channels, adhesion complexes, scaffolds, regulatory machinery, and trafficking proteins, all required for their proper function and plasticity. Additionally, while electrical synapses are often viewed as strictly symmetric structures, emerging evidence has shown that some components forming electrical synapses can be differentially distributed at each side of the junction. We propose that the molecular complexity and asymmetric distribution of proteins at the electrical synapse provides rich potential for functional diversity. © 2016 Wiley Periodicals, Inc. Develop Neurobiol 77: 562-574, 2017.

Indexed as

Electrical SynapsesGap JunctionsAnimalsconnexinelectrical synapsegap junctioninnexinsynapse formation and plasticity

Identifiers

PMID28170151
PMCPMC5395309

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.