Evidence map›Paper›PMID 39565586›Full record

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

Use of Microfluidics for Study of FOXO3 Translocation Dynamics.

Juliana Manosalva Pérez, Diego Megías

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. 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.

Juliana Manosalva PérezAdvanced Optical Microscopy Unit, Central Core Facilities, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Diego MegíasAdvanced Optical Microscopy Unit, Central Core Facilities, Instituto de Salud Carlos III (ISCIII), Madrid, Spain. diego.megias@isciii.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microfluidics has emerged as a novel tool in the study of cellular dynamics, offering a precise control of cell microenvironment and real-time analysis of intracellular processes. This chapter explores the application of microfluidic technology in the translocation dynamics of the forkhead box O3 (FOXO3) transcription factor. FOXO3 is regulator of cellular homeostasis, apoptosis, and oxidative stress responses. By integrating microfluidic devices with live cell imaging techniques, we achieve fine-tuned manipulation of extracellular conditions, including pharmacological treatments, to observe their effects on FOXO3 localization at single-cell resolution. Microfluidic devices provide a versatile and precise platform for studying dynamic cellular processes such as FOXO3-GFP translocation. This methodology allows for the real-time observation and quantification of protein translocation in response to various stimuli, enhancing our understanding of cellular signaling mechanisms.

Indexed as

Forkhead Box Protein O3Protein TransportGreen Fluorescent ProteinsHumansLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesMicrofluidicsSignal TransductionSingle-Cell AnalysisForkhead Box Protein O3FOXO3 protein, humanGreen Fluorescent ProteinsFluorescence microscopyFOXO3Live cell imagingMicrofluidics

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.