Evidence map›Paper›PMID 42577759›Full record

ArticleBio-protocol2026

Dual Color tau-STED Super Resolution Microscopy in

Louise Fougère, Christel Poujol, Yohann Boutté, Magali Grison

Abstract read
In one paragraph

Article in Bio-protocol, 2026. 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
–field-weighted citation impact
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.

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

4 authors.

Louise FougèreLaboratoire de Biogenese Membranaire, UMR5200, CNRS, Universite de Bordeaux, 33140 Villenave d'Ornon, France.
Christel PoujolUniversité de Bordeaux, CNRS, INSERM, Bordeaux Imaging Center (BIC), US4, UAR 3420, 33000 Bordeaux, France.
Yohann BouttéLaboratoire de Biogenese Membranaire, UMR5200, CNRS, Universite de Bordeaux, 33140 Villenave d'Ornon, France.
Magali GrisonLaboratoire de Biogenese Membranaire, UMR5200, CNRS, Universite de Bordeaux, 33140 Villenave d'Ornon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Super-resolution microscopy has transformed our ability to visualize subcellular structures, but its application in plant biology remains challenging due to the optical complexity of plant tissues. Here, we present a detailed protocol for tau-STED microscopy (Leica Microsystems), which combines stimulated emission depletion (STED) with fluorescence lifetime imaging (FLIM) to achieve nanoscale resolution while minimizing phototoxicity. This method leverages time-correlated single-photon counting (TCSPC) to separate fluorescence signals based on their lifetimes, enhancing signal specificity and enabling the visualization of elusive subcellular compartments in

Indexed as

Arabidopsis thalianaCell biologyLifetimePlant biologySTEDSuper-resolution microscopytau-STED

Identifiers

PMID42577759
PMCPMC13454947

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.