Evidence map›Paper›PMID 38006505›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Single-Cell PET Imaging and Tracking.

Kyung Oh Jung, Guillem Pratx

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 1 institution in 2 countries.

Kyung Oh JungDepartment of Radiation Oncology, Stanford University, Stanford, CA, USA.
Guillem PratxDepartment of Radiation Oncology, Stanford University, Stanford, CA, USA. pratx@stanford.edu.
Stanford University · US

Funding

New tools for tracking single cells in vivoR01EB030367 · NIBIB · STANFORD UNIVERSITY · PI PRATX, GUILLEM, SPRIET, MATHIEU · 2020 to 2024
$2.4M
NIBIB NIH HHS R01 EB030367
6 · The paper itself

Abstract

Positron emission tomography (PET) is one of the most sensitive whole-body molecular imaging techniques available in the clinic, able to detect picomolar levels of probe. As such, it was recently demonstrated that PET could also be used to track single radiolabeled cells in small animals. In this protocol, we present detailed procedures for radiolabeling cells using mesoporous silica nanoparticles (MSNs) and for tracking these cells in real time using in vivo PET. This includes static imaging of single cells as well as dynamic tracking of moving cells directly from the list-mode data. The protocol provides detailed instructions and examples for each step.

Indexed as

NanoparticlesPositron-Emission TomographyAnimalsWhole Body ImagingCancer metastasisCell trackingNanotechnologyPositron emission tomography

Identifiers

PMID38006505
PMCPMC11265509
OpenAlexW4388998164

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.