Evidence map›Paper›PMID 40380073›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

A Protocol for Live Imaging of Arabidopsis Gynoecium Development Using Confocal Microscopy.

Juan Ramos-Pulido, Stefan de Folter

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Juan Ramos-PulidoUnidad de Genómica Avanzada (UGA), Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (Cinvestav), Irapuato, Guanajuato, México.
Stefan de FolterUnidad de Genómica Avanzada (UGA), Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (Cinvestav), Irapuato, Guanajuato, México. stefan.defolter@cinvestav.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the Arabidopsis reproductive process, the female whorl of the flower, known as the gynoecium, passes seven of the 20 floral stages during its development. In each of these seven stages, specific developmental events occur, ranging from gynoecium primordium establishment to complex tissue and organ differentiation. Studying gynoecium development is important for its role in fruit and seed formation. Currently, there are many Arabidopsis lines with fluorescent proteins that provide relevant information on gynoecium patterning. However, the fluorescence of some proteins is affected during the steps of histological techniques. Furthermore, the complexity of gynoecium development makes live imaging difficult in the early stages and medial tissues. To address these issues at hand, we describe a methodology that facilitates the analysis of the fluorescent signal during gynoecium development, using as an example the pMIR164c::VENUS line.

Indexed as

ArabidopsisFlowersMicroscopy, ConfocalArabidopsisConfocal microscopyGynoecium developmentLive imagingMIR164miRNA

Identifiers

What OpenQuestion holds

Textmetadata
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.