Evidence map›Paper›PMID 28426025›Full record

ArticleNature protocols2017

Modular low-light microscope for imaging cellular bioluminescence and radioluminescence.

Tae Jin Kim, Silvan Türkcan, Guillem Pratx

Open access · greenAbstract read
In one paragraph

Article in Nature protocols, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Increased [Npj imaging · 2024
    Article
  5. Development of a Lensless Radiomicroscope for Cellular-Resolution Radionuclide Imaging.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Flow radiocytometry using droplet optofluidics.Biosensors & bioelectronics · 2021
    Article
  10. Article
  11. Article
  12. High-resolution radioluminescence microscopy of FDG uptake in an engineered 3D tumor-stoma model.European journal of nuclear medicine and molecular imaging · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Visualization of Mitochondrial CaInternational journal of molecular sciences · 2019
    Article
  17. Thermochemiluminescent peroxide crystals.Nature communications · 2019
    Article
  18. Review
  19. Article
  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

3 authors at 1 institution in 1 country.

Tae Jin KimDepartment of Radiation Oncology, Division of Medical Physics, Stanford University School of Medicine, Palo Alto, California, USA.
Silvan TürkcanDepartment of Radiation Oncology, Division of Medical Physics, Stanford University School of Medicine, Palo Alto, California, USA.
Guillem PratxDepartment of Radiation Oncology, Division of Medical Physics, Stanford University School of Medicine, Palo Alto, California, USA.
Stanford University · US

Funding

Stanford Molecular Imaging Scholars (SMIS) ProgramT32CA118681 · NCI · STANFORD UNIVERSITY · PI CRAIG S LEVIN · 2016 to 2026
$4.3M
Quantitative Imaging of Cancer Drug Resistance via Radioluminescence MicroarraysR01CA186275 · NCI · STANFORD UNIVERSITY · PI PRATX, GUILLEM · 2014 to 2018
$1.7M
High-throughput radionuclide counting and sorting of single cellsR21CA193001 · NCI · STANFORD UNIVERSITY · PI PRATX, GUILLEM · 2015 to 2017
$698k
NCI NIH HHS R01 CA186275NCI NIH HHS R21 CA193001NCI NIH HHS T32 CA118681
6 · The paper itself

Abstract

Low-light microscopy methods are receiving increased attention as new applications have emerged. One such application is to allow longitudinal imaging of light-sensitive cells with no phototoxicity and no photobleaching of fluorescent biomarkers. Another application is for imaging signals that are inherently dim and undetectable using standard microscopy techniques, such as bioluminescence, chemiluminescence or radioluminescence. In this protocol, we provide instructions on how to build a modular low-light microscope (1-4 d) by coupling two microscope objective lenses, back to back from each other, using standard optomechanical components. We also provide directions on how to image dim signals such as those of radioluminescence (1-1.5 h), bioluminescence (∼30 min) and low-excitation fluorescence (∼15 min). In particular, radioluminescence microscopy is explained in detail, as it is a newly developed technique that enables the study of small-molecule transport (e.g., radiolabeled drugs, metabolic precursors and nuclear medicine contrast agents) by single cells without perturbing endogenous biochemical processes. In this imaging technique, a scintillator crystal (e.g., CdWO

Indexed as

Image Processing, Computer-AssistedLuminescent MeasurementsMicroscopySingle-Cell Analysis

Identifiers

PMID28426025
PMCPMC5578809
OpenAlexW2607141745

What OpenQuestion holds

Textmetadata
LicenceTDM
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.