ReviewJournal of microscopy2011
Highlights of the optical highlighter fluorescent proteins.
Review in Journal of microscopy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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
11 citing papers in PubMed, 35 citations in OpenAlex.
- Ultrafast Dynamics of rsCherryRev in Comparison with mCherry Reflecting Its Reversive Switchability.The journal of physical chemistry. B · 2026Article
- Labeling and Tracking Mitochondria with Photoactivation inBio-protocol · 2022Article
- Photoconvertible Behavior of LSSmOrange Applicable for Single Emission Band Optical Highlighting.Biophysical journal · 2016Article
- WONOEP appraisal: molecular and cellular imaging in epilepsy.Epilepsia · 2015Review
- Three-dimensional photoactivated localization microscopy with genetically expressed probes.Methods in molecular biology (Clifton, N.J.) · 2015Article
- Super-resolution molecular and functional imaging of nanoscale architectures in life and materials science.Frontiers in bioengineering and biotechnology · 2014Review
- Ultrahigh accuracy imaging modality for super-localization microscopy.Nature methods · 2013Article
- Visualizing cell structure and function with point-localization superresolution imaging.Developmental cell · 2012Review
- Superresolution microscopy for microbiology.Cellular microbiology · 2012Review
- Two-photon activated two-photon fluorescence and binding of azidocoumarin in a gelatin matrix.Journal of fluorescence · 2012Article
- Optical highlighter molecules in neurobiology.Current opinion in neurobiology · 2012Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
Abstract
The development of super-resolution microscopy techniques using molecular localization, such as photoactivated localization microscopy, fluorescence photoactivated localization microscopy, stochastic optical reconstruction microscopy, photoactivated localization microscopy with independent running acquisition and many others, has heightened interest in molecules that will be grouped here into a category referred to as 'optical highlighter' fluorescent proteins. This review will survey many of the advances in development of fluorescent proteins for optically highlighting sub-populations of fluorescently labelled molecules.
Indexed as
Identifiers
What 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.