Evidence map›Paper›PMID 24876996›Full record

ArticleBiomedical optics express2014

Cellular imaging of deep organ using two-photon Bessel light-sheet nonlinear structured illumination microscopy.

Ming Zhao, Han Zhang, Yu Li, Amit Ashok, Rongguang Liang, Weibin Zhou, Leilei Peng

Open access · goldAbstract read
In one paragraph

Article in Biomedical optics express, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 75 citations in OpenAlex.

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  10. In vivo NIR-II structured-illumination light-sheet microscopy.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  20. Novel Microscopic Techniques for Podocyte Research.Frontiers in endocrinology · 2018
    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

7 authors at 2 institutions in 1 country.

Ming ZhaoCollege of Optical Sciences, the University of Arizona, 1630 East University Blvd., Tucson, AZ 85721, USA.
Han ZhangCollege of Optical Sciences, the University of Arizona, 1630 East University Blvd., Tucson, AZ 85721, USA.
Yu LiCollege of Optical Sciences, the University of Arizona, 1630 East University Blvd., Tucson, AZ 85721, USA.
Amit AshokCollege of Optical Sciences, the University of Arizona, 1630 East University Blvd., Tucson, AZ 85721, USA.
Rongguang LiangCollege of Optical Sciences, the University of Arizona, 1630 East University Blvd., Tucson, AZ 85721, USA.
Weibin ZhouDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan, MI 48109, USA.
Leilei PengCollege of Optical Sciences, the University of Arizona, 1630 East University Blvd., Tucson, AZ 85721, USA.
University of Arizona · USUniversity of Michigan–Ann Arbor · US

Funding

University of Michigan O'Brien Kidney Translational Core CenterP30DK081943 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PENNATHUR, SUBRAMANIAM · 2008 to 2022
$12.9M
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
Mesonephric Model of Podocyte Injury and RegenerationR00DK091405 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHOU, WEIBIN · 2013 to 2015
$730k
Super-resolution Full-field Stimulated Emission Depletion Microscope by StructureR21EB012646 · NIBIB · UNIVERSITY OF ARIZONA · PI PENG, LEILEI · 2012 to 2013
$383k
NIBIB NIH HHS R00 EB008737NIBIB NIH HHS R01 EB015481NIBIB NIH HHS R21 EB012646NIDDK NIH HHS P30 DK081943NIDDK NIH HHS R00 DK091405
6 · The paper itself

Abstract

In vivo fluorescent cellular imaging of deep internal organs is highly challenging, because the excitation needs to penetrate through strong scattering tissue and the emission signal is degraded significantly by photon diffusion induced by tissue-scattering. We report that by combining two-photon Bessel light-sheet microscopy with nonlinear structured illumination microscopy (SIM), live samples up to 600 microns wide can be imaged by light-sheet microscopy with 500 microns penetration depth, and diffused background in deep tissue light-sheet imaging can be reduced to obtain clear images at cellular resolution in depth beyond 200 microns. We demonstrate in vivo two-color imaging of pronephric glomeruli and vasculature of zebrafish kidney, whose cellular structures located at the center of the fish body are revealed in high clarity by two-color two-photon Bessel light-sheet SIM.

Indexed as

(170.2520) Fluorescence microscopy(170.6900) Three-dimensional microscopy

Identifiers

PMID24876996
PMCPMC4026892
OpenAlexW1970520671

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.