Evidence map›Paper›PMID 24589986›Full record

ArticleJournal of biomedical optics2014

Integrated photoacoustic, confocal, and two-photon microscope.

Bin Rao, Florentina Soto, Daniel Kerschensteiner, Lihong V Wang

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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  17. Review
  18. Article
  19. Photoacoustic imaging platforms for multimodal imaging.Ultrasonography (Seoul, Korea) · 2015
    Review
  20. 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

4 authors.

Bin RaoWashington University in St. Louis, Optical Imaging Laboratory, Department of Biomedical Engineering, One Brookings Drive, St. Louis, Missouri 63130.
Florentina SotoWashington University School of Medicine, Department of Ophthalmology and Visual Sciences, Box 8096, St. Louis, Missouri 63110.
Daniel KerschensteinerWashington University School of Medicine, Department of Ophthalmology and Visual Sciences, Box 8096, St. Louis, Missouri 63110.
Lihong V WangWashington University in St. Louis, Optical Imaging Laboratory, Department of Biomedical Engineering, One Brookings Drive, St. Louis, Missouri 63130.

Funding

PHOTON TUNNELING: SHEDDING NEW LIGHT ON BIOMEDICINEDP1EB016986 · NIBIB · WASHINGTON UNIVERSITY · PI WANG, LIHONG · 2012 to 2016
$3.8M
PHOTOACOUSTIC MICROSCOPY OF NEOVASCULARIZATION IN RENAL CANCER GROWTH AND THERAPYR01CA159959 · NCI · WASHINGTON UNIVERSITY · PI ARBEIT, JEFFREY MICHAEL · 2011 to 2015
$2.9M
SPATIAL CELL BIOLOGY OF RETINAL CIRCUIT DEVELOPMENTR01EY021855 · NEI · WASHINGTON UNIVERSITY · PI KERSCHENSTEINER, DANIEL · 2011 to 2015
$1.9M
INTEGRATED TWO-PHOTON/CONFOCAL/PHOTOACOUSTIC MICROSCOPYS10RR028864 · NCRR · WASHINGTON UNIVERSITY · PI WANG, LIHONG · 2010 to 2010
$1.2M
Smart Laser Treatment of Port-Wine Stain in ChildrenK99AR062530 · NIAMS · WASHINGTON UNIVERSITY · PI RAO, BIN · 2012 to 2013
$172k
NCCDPHP CDC HHS DP1 EB016986NCI NIH HHS R01 CA159959NCRR NIH HHS 1S10RR028864NCRR NIH HHS S10 RR028864NEI NIH HHS R01 EY021855NIAMS NIH HHS K99 AR062530NIAMS NIH HHS K99AR062530NIBIB NIH HHS DP1 EB016986
6 · The paper itself

Abstract

The invention of green fluorescent protein and other molecular fluorescent probes has promoted applications of confocal and two-photon fluorescence microscopy in biology and medicine. However, exogenous fluorescence contrast agents may affect cellular structure and function, and fluorescence microscopy cannot image nonfluorescent chromophores. We overcome this limitation by integrating optical-resolution photoacoustic microscopy into a modern Olympus IX81 confocal, two-photon, fluorescence microscope setup to provide complementary, label-free, optical absorption contrast. Automatically coregistered images can be generated from the same sample. Imaging applications in ophthalmology, developmental biology, and plant science are demonstrated. For the first time, in a familiar microscopic fluorescence imaging setting, this trimodality microscope provides a platform for future biological and medical discoveries.

Indexed as

AnimalsEmbryo, NonmammalianFluorescent DyesHistocytochemistryLuminescent ProteinsMiceMice, TransgenicMicroscopy, ConfocalMicroscopy, Fluorescence, MultiphotonPhotoacoustic TechniquesRetinaZebrafishFluorescent DyesLuminescent Proteins

Identifiers

PMID24589986
PMCPMC3939434

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.