Evidence map›Paper›PMID 29570774›Full record

ArticleJournal of microscopy2018

Application of the Mesolens for subcellular resolution imaging of intact larval and whole adult Drosophila.

G McConnell, W B Amos

Open access · hybridAbstract read
In one paragraph

Article in Journal of microscopy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Mesolens imaging in microbiology.Essays in biochemistry · 2026
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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

2 authors at 2 institutions in 1 country.

G McConnellDepartment of Physics, SUPA, University of Strathclyde, Glasgow, U.K.ORCID 0000-0002-7213-0686
W B AmosDepartment of Physics, SUPA, University of Strathclyde, Glasgow, U.K.
MRC Laboratory of Molecular Biology · GBUniversity of Strathclyde · GB

Funding

Medical Research Council MC_U105184326Medical Research Council MR/K015583/1
6 · The paper itself

Abstract

In a previous paper, we showed a new giant lens called the Mesolens and presented performance data and images from whole fixed and intact fluorescently-stained 12.5-day old mouse embryos. Here, we show that using the Mesolens we can image an entire Drosophila larva or adult fly in confocal epifluorescence and show subcellular detail in all tissues. By taking several hundreds of optical sections through the entire volume of the specimen, we show cells and nuclear details within the gut, brain, salivary glands and reproductive system that normally require dissection for study. Organs are imaged in situ in correct 3D arrangement. Imaginal discs are imaged in mature larvae and it proved possible to image pachytene chromosomes in cells within ovarian follicles in intact female flies. Methods for fixing, staining and clearing are given.

Indexed as

AnimalsAnimal StructuresDrosophilaImaging, Three-DimensionalLarvaMicroscopy, ConfocalMicroscopy, FluorescenceConfocalDrosophilaimagolarvaMesolenssubcellular

Identifiers

PMID29570774
PMCPMC5947746
OpenAlexW2790459678

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.