Evidence map›Paper›PMID 27676647›Full record

ArticleZebrafish2017

zWEDGI: Wounding and Entrapment Device for Imaging Live Zebrafish Larvae.

Kayla Huemer, Jayne M Squirrell, Robert Swader, Danny C LeBert, Anna Huttenlocher, Kevin W Eliceiri

Open access · greenAbstract read
In one paragraph

Article in Zebrafish, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

37 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  7. Macrophage vacuolar ATPase (v-ATPase) function controlsbioRxiv : the preprint server for biology · 2025
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  8. Co-zorbs: Motile, multispecies biofilms aid transport of diverse bacterial species.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  19. bioRxiv : the preprint server for biology · 2023
    Article
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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

6 authors at 3 institutions in 1 country.

Kayla Huemer1 Morgridge Institute for Research , Madison, Wisconsin.
Jayne M Squirrell3 Laboratory for Optical and Computational Instrumentation, UW-Madison , Madison, Wisconsin.
Robert Swader1 Morgridge Institute for Research , Madison, Wisconsin.
Danny C LeBert4 Cellular and Molecular Pathology Graduate Program, UW-Madison , Madison, Wisconsin.
Anna Huttenlocher5 Department of Medical Microbiology and Immunology.
Kevin W Eliceiri1 Morgridge Institute for Research , Madison, Wisconsin.
Computational Sciences (United States) · USMorgridge Institute for Research · USUniversity of Wisconsin–Madison · US

Funding

A toolkit for imaging and photo-manipulation of signaling in zebrafishR01GM102924 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HAHN, KLAUS M., HUTTENLOCHER, ANNA · 2012 to 2015
$2.5M
Graduate Training In Cellular And Molecular Pathogenesis Of Human DiseasesT32GM081061 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FABRY, ZSUZSANNA · 2010 to 2019
$1.8M
NIGMS NIH HHS R01 GM102924NIGMS NIH HHS T32 GM081061
6 · The paper itself

Abstract

Zebrafish, an established model organism in developmental biology, is also a valuable tool for imaging wound healing in space and time with cellular resolution. However, long-term imaging of wound healing poses technical challenges as wound healing occurs over multiple temporal scales. The traditional strategy of larval encapsulation in agarose successfully limits sample movement but impedes larval development and tissue regrowth and is therefore not amenable to long-term imaging of wound healing. To overcome this challenge, we engineered a functionally compartmentalized device, the zebrafish Wounding and Entrapment Device for Growth and Imaging (zWEDGI), to orient larvae for high-resolution microscopy, including confocal and second harmonic generation (SHG), while allowing unrestrained tail development and regrowth. In this device, larval viability was maintained and tail regrowth was improved over embedding in agarose. The quality of tail fiber SHG images collected from larvae in the device was similar to fixed samples but provided the benefit of time lapse data collection. Furthermore, we show that this device was amenable to long-term (>24 h) confocal microscopy of the caudal fin. Finally, the zWEDGI was designed and fabricated using readily available techniques so that it can be easily modified for diverse experimental imaging protocols.

Indexed as

AnimalsDevelopmental BiologyEquipment DesignImage Processing, Computer-AssistedImaging, Three-DimensionalLarvaMicroscopy, ConfocalMicroscopy, Fluorescence, MultiphotonWound HealingZebrafishdevicelive imagingmicroscopywounding

Identifiers

PMID27676647
PMCPMC5312606
OpenAlexW2524695962

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.