Evidence map›Paper›PMID 31729201›Full record

ArticleJournal of biomedical optics2019

Demonstration of flat-top beam illumination in widefield multiphoton microscopy.

Mohammad Kabir, Hemangg Rajput, Varun Kelkar, Adriana Salazar Coariti, Kimani Toussaint

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Mohammad KabirUniv. of Illinois, United States.
Hemangg RajputLab. for Photonics Research of Bio/Nano Environments, United States.
Varun KelkarUniv. of Illinois, United States.
Adriana Salazar CoaritiLab. for Photonics Research of Bio/Nano Environments, United States.
Kimani ToussaintLab. for Photonics Research of Bio/Nano Environments, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiphoton microscopy provides a suitable technique for imaging biological tissues with submicrometer resolution. Usually a Gaussian beam (GB) is used for illumination, leading to a reduced power efficiency in the multiphoton response and vignetting for a square-shaped imaging area. A flat-top beam (FTB) provides a uniform spatial intensity distribution that equalizes the probability of a multiphoton effect across the imaging area. We employ a customized widefield multiphoton microscope to compare the performance of a square-shaped FTB illumination with that based on using a GB, for both two-photon fluorescence (TPF) and second-harmonic generation (SHG) imaging. The variation in signal-to-noise ratio across TPF images of fluorescent dyes spans ∼5.6  dB for the GB and ∼1.2  dB for the FTB illumination, respectively. For the GB modality, TPF images of mouse colon and

Indexed as

AnimalsBreastChickensColonComputer SimulationConvallariaEquipment DesignFemaleFluorescent DyesHumansMathematical ConceptsMiceMicroscopy, Fluorescence, MultiphotonOptical ImagingOptical PhenomenaSignal-To-Noise RatioFluorescent Dyesflat-top beammultiphoton microscopysecond-harmonic generationtwo-photon fluorescenceuniform illumination

Identifiers

PMID31729201
PMCPMC7008505

What OpenQuestion holds

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Registered trials

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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.