Evidence map›Paper›PMID 31601843›Full record

ArticleScientific reports2019

Three-Dimensional Microscopy by Milling with Ultraviolet Excitation.

Jiaming Guo, Camille Artur, Jason L Eriksen, David Mayerich

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 3D imaging of the vagus nerve fascicular anatomy with cryo-imaging and UV excitation.Proceedings of SPIE--the International Society for Optical Engineering · 2021
    Article
  8. Three-Dimensional Imaging in Stem Cell-Based Researches.Frontiers in veterinary science · 2021
    Review
  9. 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.

Jiaming GuoUniversity of Houston, Department of Electrical and Computer Engineering, Houston, USA.ORCID http://orcid.org/0000-0002-8189-846X
Camille ArturUniversity of Houston, Department of Electrical and Computer Engineering, Houston, USA.
Jason L EriksenUniversity of Houston, College of Pharmacy, Department of Pharmacological and Pharmaceutical Sciences, Houston, USA.ORCID http://orcid.org/0000-0003-1549-4165
David MayerichUniversity of Houston, Department of Electrical and Computer Engineering, Houston, USA. mayerich@uh.edu.ORCID http://orcid.org/0000-0002-3949-6133

Funding

Structural and Molecular Phenotyping of Embryonic Development through Multi-Modal Optical ImagingR01HL146745 · NHLBI · UNIVERSITY OF HOUSTON · PI MAYERICH, DAVID · 2019 to 2023
$3.7M
A Vascularized, In Vitro, Organotropic Metastasis Model to Generate Dormant MicrometastasesR21CA214299 · NCI · UNIVERSITY OF DELAWARE · PI SLATER, JOHN HUNDLEY · 2017 to 2019
$588k
NCI NIH HHS R21 CA214299NHLBI NIH HHS R01 HL146745
6 · The paper itself

Abstract

Analysis of three-dimensional biological samples is critical to understanding tissue function and the mechanisms of disease. Many chronic conditions, like neurodegenerative diseases and cancers, correlate with complex tissue changes that are difficult to explore using two-dimensional histology. While three-dimensional techniques such as confocal and light-sheet microscopy are well-established, they are time consuming, require expensive instrumentation, and are limited to small tissue volumes. Three-dimensional microscopy is therefore impractical in clinical settings and often limited to core facilities at major research institutions. There would be a tremendous benefit to providing clinicians and researchers with the ability to routinely image large three-dimensional tissue volumes at cellular resolution. In this paper, we propose an imaging methodology that enables fast and inexpensive three-dimensional imaging that can be readily integrated into current histology pipelines. This method relies on block-face imaging of paraffin-embedded samples using deep-ultraviolet excitation. The imaged surface is then ablated to reveal the next tissue section for imaging. The final image stack is then aligned and reconstructed to provide tissue models that exceed the depth and resolution achievable with modern three-dimensional imaging systems.

Indexed as

Ultraviolet RaysAnimalsBrainCerebral CortexHumansImage Processing, Computer-AssistedImaging, Three-DimensionalLiverLungMiceMicrocirculationMicroscopyMicroscopy, ConfocalMicroscopy, UltravioletMicrotomyMonte Carlo Method

Identifiers

PMID31601843
PMCPMC6787072

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.