Evidence map›Paper›PMID 24298028›Full record

ArticleCold Spring Harbor protocols2013

Combining Ca2+ imaging with -glutamate photorelease.

Marco Canepari, Michel De Waard, David Ogden

Abstract read
In one paragraph

Article in Cold Spring Harbor protocols, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Marco CanepariInserm U836, Team 3, BP 170, Grenoble cedex 09, F-38042, France;
Michel De Waard
David Ogden

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This article describes simple configurations and methods for measuring optical Ca(2+) signals in response to photorelease of -glutamate. This photostimulation allows activation of postsynaptic glutamate receptors without activation of voltage-gated Ca(2+) channels, thereby permitting the separation and analysis of different Ca(2+) components. We give details of basic microscopy configurations and recommend tools for efficiently illuminating the preparation while preserving the healthy condition of the tissue. We also suggest methodological procedures and discuss linear optics for achieving simultaneous imaging and uncaging using two-photon illumination.

Indexed as

BrainCalciumCations, DivalentGlutamic AcidMicroscopy, FluorescenceNeuronsOptical ImagingPhysiological PhenomenaSynapsesCalciumCations, DivalentGlutamic Acid

Identifiers

PMID24298028
PMCPMC5225263

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.