Evidence map›Paper›PMID 33649665›Full record

ArticleOptics letters2021

Multicolor fiber-optic two-photon endomicroscopy for brain imaging.

Honghua Guan, Wenxuan Liang, Ang Li, Yung-Tian A Gau, Defu Chen, Ming-Jun Li, Dwight E Bergles, Xingde Li

Abstract read
In one paragraph

Article in Optics letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  6. Review
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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

8 authors.

Honghua Guan
Wenxuan Liang
Ang Li
Yung-Tian A Gau
Defu Chen
Ming-Jun Li
Dwight E Bergles
Xingde Li

Funding

Nonlinear Optical Endomicroscopy for Optical Biopsy of Cancer in Internal OrgansR01CA153023 · NCI · JOHNS HOPKINS UNIVERSITY · PI LI, XINGDE · 2011 to 2015
$2.6M
NCI NIH HHS R01 CA153023
6 · The paper itself

Abstract

Visualizing activity patterns of distinct cell types during complex behaviors is essential to understand complex neural networks. It remains challenging to excite multiple fluorophores simultaneously so that different types of neurons can be imaged. In this Letter, we report a multicolor fiber-optic two-photon endomicroscopy platform in which two pulses from a Ti:sapphire laser and an optical parametric oscillator were synchronized and delivered through a single customized double-clad fiber to excite multiple chromophores. A third virtual wavelength could also be generated by spatial-temporal overlapping of the two pulses. The performance of the fiber-optic multicolor two-photon endomicroscope was demonstrated by in vivo imaging of a mouse cerebral cortex with "Brainbow" labeling.

Indexed as

BrainOptical FibersAnimalsColorFiber Optic TechnologyMiceMicroscopy, Fluorescence, MultiphotonPhotons

Identifiers

PMID33649665
PMCPMC11214692

What OpenQuestion holds

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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.