Evidence map›Paper›PMID 29760977›Full record

ArticleBiomedical optics express2018

Fast volume-scanning light sheet microscopy reveals transient neuronal events.

Peter Haslehurst, Zhengyi Yang, Kishan Dholakia, Nigel Emptage

Abstract read
In one paragraph

Article in Biomedical optics express, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

4 authors.

Peter HaslehurstDepartment of Pharmacology, University of Oxford, Oxford, OX1 3QT, UK.
Zhengyi YangSUPA, School of Physics & Astronomy, University of St Andrews, St Andrews, KY16 9SS, UK.
Kishan DholakiaSUPA, School of Physics & Astronomy, University of St Andrews, St Andrews, KY16 9SS, UK.
Nigel EmptageDepartment of Pharmacology, University of Oxford, Oxford, OX1 3QT, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/J018724/1
6 · The paper itself

Abstract

Light sheet fluorescence microscopy offers considerable potential to the cellular neuroscience community as it makes it possible to image extensive areas of neuronal structures, such as axons or dendrites, with a low light budget, thereby minimizing phototoxicity. However, the shallow depth of a light sheet, which is critical for achieving high contrast, well resolved images, adds a significant challenge if fast functional imaging is also required, as multiple images need to be collected across several image planes. Consequently, fast functional imaging of neurons is typically restricted to a small tissue volume where part of the neuronal structure lies within the plane of a single image. Here we describe a method by which fast functional imaging can be achieved across a much larger tissue volume; a custom-built light sheet microscope is presented that includes a synchronized galvo mirror and electrically tunable lens, enabling high speed acquisition of images across a configurable depth. We assess the utility of this technique by acquiring fast functional Ca

Indexed as

(170.0180) Microscopy(170.2655) Functional monitoring and imaging(170.3880) Medical and biological imaging(180.2520) Fluorescence microscopy

Identifiers

PMID29760977
PMCPMC5946778

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Registered trials

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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.