Evidence map›Paper›PMID 31015706›Full record

ArticleNature biomedical engineering2017

Microscopy with ultraviolet surface excitation for rapid slide-free histology.

Farzad Fereidouni, Zachary T Harmany, Miao Tian, Austin Todd, John A Kintner, John D McPherson, Alexander D Borowsky, John Bishop, Mirna Lechpammer, Stavros G Demos and 1 more

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing 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

145 citing papers in PubMed.

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85 more citing papers are in PubMed but not listed here.

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

11 authors.

Farzad FereidouniDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
Zachary T HarmanyDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.ORCID http://orcid.org/0000-0002-5871-1783
Miao TianDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
Austin ToddDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
John A KintnerDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
John D McPhersonDepartment of Biochemistry and Molecular Medicine, University of California Davis Medical Center, Sacramento, CA, USA.ORCID http://orcid.org/0000-0001-8049-9347
Alexander D BorowskyDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
John BishopDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
Mirna LechpammerDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA.
Stavros G DemosLawrence Livermore National Laboratory, Livermore, CA, USA.
Richard LevensonDepartment of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA, USA. levenson@ucdavis.edu.ORCID http://orcid.org/0000-0002-0112-6823

Funding

Imaging and informatics techniques to spatially map tumor-associated collagen: novel cancer diagnostic tools (2 of 2)R33CA202881 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEVENSON, RICHARD M. · 2017 to 2019
$1.3M
NCI NIH HHS R33 CA202881
6 · The paper itself

Abstract

Histological examination of tissues is central to the diagnosis and management of neoplasms and many other diseases and is a foundational technique for preclinical and basic research. However, commonly used bright-field microscopy requires prior preparation of micrometre-thick tissue sections mounted on glass slides-a process that can require hours or days, contributes to cost and delays access to critical information. Here, we introduce a simple, non-destructive slide-free technique that, within minutes, provides high-resolution diagnostic histological images resembling those obtained from conventional haematoxylin and eosin histology. The approach, which we named microscopy with ultraviolet surface excitation (MUSE), can also generate shape and colour-contrast information. MUSE relies on ~280 nm ultraviolet light to restrict the excitation of conventional fluorescent stains to tissue surfaces and it has no significant effects on downstream molecular assays (including fluorescence in situ hybridization and RNA sequencing). MUSE promises to improve the speed and efficiency of patient care in both state-of-the-art and low-resource settings and to provide opportunities for rapid histology in research.

Indexed as

AnimalsCarcinomaHistological TechniquesHumansImage Processing, Computer-AssistedMicroscopy, UltravioletMolecular Diagnostic TechniquesPathologyReproducibility of ResultsUltraviolet Rays

Identifiers

PMID31015706
PMCPMC6223324

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.