Evidence map›Paper›PMID 34796706›Full record

ArticleJournal of biomedical optics2021

Two-photon scanned light sheet fluorescence microscopy with axicon imaging for fast volumetric imaging.

Po-Yen Lin, Sheng-Ping L Hwang, Chi-Hon Lee, Bi-Chang Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Structural and functional imaging of brains.Science China. Chemistry · 2023
    Review
  4. 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.

Po-Yen LinInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Sheng-Ping L HwangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Chi-Hon LeeInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Bi-Chang ChenInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Institute of Cellular and Organismic Biology, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

significanceTwo-photon microscopy has become the standard platform for deep-tissue fluorescence imaging. However, the use of point scanning in conventional two-photon microscopy limits the speed of volumetric image acquisition.

aimTo obtain fast and deep volumetric images, we combine two-photon light sheet fluorescence microscopy (2p-LSFM) and axicon imaging that yields an extended depth of field (DOF) in 2p-LSFM. APPROACH: Axicon imaging is achieved by imposing an axicon lens in the detection part of LSFM.

resultsThe DOF with axicon imaging is extended more than 20-fold over that of a conventional imaging lens, liberating the synchronized scanning in LSFM. We captured images of dynamic beating hearts and red blood cells in zebrafish larvae at volume acquisition rates up to 30 Hz.

conclusionsWe demonstrate the fast three-dimensional imaging capability of 2p-LSFM with axicon imaging by recording the rapid dynamics of physiological processes.

Indexed as

LensesZebrafishAnimalsImaging, Three-DimensionalMicroscopy, Fluorescencelight sheet fluorescence microscopythree-dimensional imagingtwo-photon microscopy

Identifiers

PMID34796706
PMCPMC8601431
OpenAlexW3213474672

What OpenQuestion holds

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LicenceCC BY
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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.