Evidence map›Paper›PMID 42642571›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Automated Measurements of Fluorescence in Spatially Defined Regions of Pollen Tubes.

Jeremy Adler, Ingela Parmryd

Abstract read
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Article in Methods in molecular biology (Clifton, N.J.), 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

2 authors.

Jeremy AdlerDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Ingela ParmrydDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden. ingela.parmryd@gu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pollen tubes are a widely used model for the extension and development of polarized cells. Their relatively standard shape simplifies automated identification and image analysis of subregions. The key is reliable identification of the cell plasma membrane and the pollen tube tip. This chapter describes how regions of interest can be created and used to assess distributions in tubular cells using two ImageJ macros. The first macro enables efficient and precise identification of the pollen tube plasma membrane and tip, based on a few imprecisely marked points. Subsequent steps are automated, with users prompted to confirm their accuracy, a balance between automation and supervision. The plasma membrane and the tip are the bases of five distance maps: three starting from the tip, one from the plasma membrane, and one from the pollen tube midline. Measurements of fluorescence intensity and generalized polarization gradients are then made from the tip along the plasma membrane. The second macro uses the distance maps to measure fluorescence intensities and generalized polarization from user-specified regions derived from a single or a combination of the five distance maps. Highly reproducible measurements are achieved by automation with minimal user interaction, while every analysis step is recorded for complete traceability.

Indexed as

Microscopy, FluorescencePollen TubeAutomationCell MembraneCell PolarityFluorescenceImage Processing, Computer-AssistedDistance mapFluorescence gradientGeneralized polarizationImageJMacroPlasma membrane identificationPollen tubesRegion of interest

Identifiers

What OpenQuestion holds

Textmetadata
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Registered trials

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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.