Evidence map›Paper›PMID 25914756›Full record

ArticleCellular and molecular bioengineering2015

Fluorescent Photo-conversion: A second chance to label unique cells.

Adam J Mellott, Heather E Shinogle, David S Moore, Michael S Detamore

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Cellular and molecular bioengineering, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 94% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Cyanine Phototruncation Enables Spatiotemporal Cell Labeling.Journal of the American Chemical Society · 2022
    Article
  3. Review
  4. 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 at 1 institution in 1 country.

Adam J MellottBioengineering Graduate Program, University of Kansas, Lawrence, Kansas 66045.
Heather E ShinogleMicroscopy and Analytical Imaging Laboratory, University of Kansas, Lawrence, Kansas 66045.
David S MooreMicroscopy and Analytical Imaging Laboratory, University of Kansas, Lawrence, Kansas 66045.
Michael S DetamoreBioengineering Graduate Program, University of Kansas, Lawrence, Kansas 66045 ; Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, Kansas 66045.
University of Kansas · US

Funding

Gradient-based strategy for osteochondral regenerationR01AR056347 · NIAMS · UNIVERSITY OF KANSAS LAWRENCE · PI DETAMORE, MICHAEL S. · 2010 to 2014
$1.3M
NIAMS NIH HHS R01 AR056347
6 · The paper itself

Abstract

Not all cells behave uniformly after treatment in tissue engineering studies. In fact, some treated cells display no signs of treatment or show unique characteristics not consistent with other treated cells. What if the "unique" cells could be isolated from a treated population, and further studied? Photo-convertible reporter proteins, such as

Indexed as

Cell trackingDendra2Human Wharton's jelly cellsNucleofectionPhoto-convertible reporter gene

Identifiers

PMID25914756
PMCPMC4406481
OpenAlexW1989095468

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.