Evidence map›Paper›PMID 24921725›Full record

ArticleOptics express2014

Parallel excitation-emission multiplexed fluorescence lifetime confocal microscopy for live cell imaging.

Ming Zhao, Yu Li, Leilei Peng

Abstract read
In one paragraph

Article in Optics express, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Fourier Multiplexed Fluorescence Lifetime Imaging.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  7. Excitation-multiplexed multicolor superresolution imaging with fm-STORM and fm-DNA-PAINT.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
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.

Ming Zhao
Yu Li
Leilei Peng

Funding

High-resolution multi-color FLIM-FRET tomography of whole organismR01EB015481 · NIBIB · UNIVERSITY OF ARIZONA · PI PENG, LEILEI · 2012 to 2015
$1.3M
Densely Multiplexed Fluorescence Imaging by Fourier Transform FluorometryR00EB008737 · NIBIB · UNIVERSITY OF ARIZONA · PI PENG, LEILEI · 2009 to 2011
$731k
NIBIB NIH HHS R00 EB008737NIBIB NIH HHS R00EB008737NIBIB NIH HHS R01 EB015481NIBIB NIH HHS R01EB015481
6 · The paper itself

Abstract

We present a novel excitation-emission multiplexed fluorescence lifetime microscopy (FLIM) method that surpasses current FLIM techniques in multiplexing capability. The method employs Fourier multiplexing to simultaneously acquire confocal fluorescence lifetime images of multiple excitation wavelength and emission color combinations at 44,000 pixels/sec. The system is built with low-cost CW laser sources and standard PMTs with versatile spectral configuration, which can be implemented as an add-on to commercial confocal microscopes. The Fourier lifetime confocal method allows fast multiplexed FLIM imaging, which makes it possible to monitor multiple biological processes in live cells. The low cost and compatibility with commercial systems could also make multiplexed FLIM more accessible to biological research community.

Indexed as

Diagnostic ImagingFluorescenceHumansMicroscopy, ConfocalMicroscopy, Fluorescence

Identifiers

PMID24921725
PMCPMC4083044

What OpenQuestion holds

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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.