ArticleJournal of fluorescence2011
Global analysis of dynamic fluorescence anisotropy by a polarized phasor approach.
Article in Journal of fluorescence, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Laurdan monitors different lipids content in eukaryotic membrane during embryonic neural development.Cell biochemistry and biophysics · 2014Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Recently, the graphical analysis of the fluorescence lifetime imaging using the phasor approach has been highlight, and a series of the reports have made it on the way for the applications by the nonprofessionals. In this paper, we put forward a similar theory validated by the experiments for the dynamic fluorescence anisotropy imaging. By subtracting the perpendicular component from the parallel one in the frequency-domain polarization measurement, we deduce a new analytical expression about the fluorescence joint time, and find that as much as the fluorophore is a single exponential decay and r∞ is equal to zero, △I(t) is a single exponential decay with the time constant X as well, and the center of its histograms is located on the semicircle in the polarized phasor plot. In the end, we conclude that the fluorescence joint time is the best parameter to weigh the fluorescence dynamics for the macromolecules.
Identifiers
20532594What OpenQuestion holds
Registered trials
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.