Evidence map›Paper›PMID 22843821›Full record

ReviewCold Spring Harbor perspectives in biology2012

Studying signal transduction in single dendritic spines.

Ryohei Yasuda

Abstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
  5. Review
  6. Article
  7. Single Synapse LTP: A Matter of Context?Frontiers in cellular neuroscience · 2019
    Review
  8. Review
  9. Article
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
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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

1 author.

Ryohei YasudaNeurobiology Department, Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710, USA. yasuda@neuro.duke.edu

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Many forms of synaptic plasticity are triggered by biochemical signaling that occurs in small postsynaptic compartments called dendritic spines, each of which typically houses the postsynaptic terminal associated with a single glutamatergic synapse. Recent advances in optical techniques allow investigators to monitor biochemical signaling in single dendritic spines and thus reveal the signaling mechanisms that link synaptic activity and the induction of synaptic plasticity. This is mostly in the study of Ca2+-dependent forms of synaptic plasticity for which many of the steps between Ca2+ influx and changes to the synapse are now known. This article introduces the new techniques used to investigate signaling in single dendritic spines and the neurobiological insights that they have produced.

Indexed as

Signal TransductionCalcium-Calmodulin-Dependent Protein Kinase Type 2Calcium SignalingDendritic SpinesFluorescence Resonance Energy TransferModels, BiologicalNeuronal Plasticityras ProteinsCalcium-Calmodulin-Dependent Protein Kinase Type 2ras Proteins

Identifiers

PMID22843821
PMCPMC3475171

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.