Evidence map›Paper›PMID 36239030›Full record

ReviewThe European journal of neuroscience2022

Exploiting the molecular diversity of the synapse to investigate neuronal communication: A guide through the current toolkit.

Jacopo Lamanna, Mattia Ferro, Sara Spadini, Antonio Malgaroli

Open access · hybridAbstract readReview
In one paragraph

Review in The European journal of neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

4 authors at 1 institution in 1 country.

Jacopo LamannaCenter for Behavioral Neuroscience and Communication (BNC), Vita-Salute San Raffaele University, Milan, Italy.ORCID 0000-0002-1919-8219
Mattia FerroCenter for Behavioral Neuroscience and Communication (BNC), Vita-Salute San Raffaele University, Milan, Italy.
Sara SpadiniCenter for Behavioral Neuroscience and Communication (BNC), Vita-Salute San Raffaele University, Milan, Italy.ORCID 0000-0002-7059-8242
Antonio MalgaroliCenter for Behavioral Neuroscience and Communication (BNC), Vita-Salute San Raffaele University, Milan, Italy.
Vita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemical synapses are tiny and overcrowded environments, deeply embedded inside brain tissue and enriched with thousands of protein species. Many efforts have been devoted to developing custom approaches for evaluating and modifying synaptic activity. Most of these methods are based on the engineering of one or more synaptic protein scaffolds used to target active moieties to the synaptic compartment or to manipulate synaptic functioning. In this review, we summarize the most recent methodological advances and provide a description of the involved proteins as well as the operation principle. Furthermore, we highlight their advantages and limitations in relation to studies of synaptic transmission in vitro and in vivo. Concerning the labelling methods, the most important challenge is how to extend the available approaches to the in vivo setting. On the other hand, for those methods that allow manipulation of synaptic function, this limit has been overcome using optogenetic approaches that can be more easily applied to the living brain. Finally, future applications of these methods to neuroscience, as well as new potential routes for development, are discussed.

Indexed as

NeuronsSynapsesBrainOptogeneticsSynaptic Transmissionendo-exocytosisgenetically encodedindicatoroptogeneticssynaptic transmission

Identifiers

PMID36239030
PMCPMC10100385
OpenAlexW4306163945

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.