Evidence map›Paper›PMID 42681008›Full record

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

Method for Analyzing Nucleoskeletal Components from the Isolated Nucleus.

Marina Armesto, Christopher P Toseland, Javier Redondo-Muñoz

Abstract read
PubMed Publisher
In one paragraph

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

3 authors.

Marina ArmestoDepartment of Biomedicine, Centro de Investigaciones Biológicas Margarita Salas, Madrid, Spain.
Christopher P ToselandSchool of Medicine and Population Health, University of Sheffield, Sheffield, UK.
Javier Redondo-MuñozDepartment of Biomedicine, Centro de Investigaciones Biológicas Margarita Salas, Madrid, Spain. Javier.redondo@cib.csic.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple skeletal components, including actin and associated proteins, are located in both the cytoplasm and the nucleus. Here, we describe a methodology to study nuclear actin and its associated proteins through a comprehensive approach. First, we focus on nuclear isolation as a singular step to separate and distinguish skeletal components within the nucleus. Nuclear actin organization can be regulated by using pharmacological agents (e.g., latrunculin, jasplakinolide) or genetic tools, such as mutants of nuclear actin (NLS-actinR62D). These approaches allow us to analyze the nuclear morphology, protein localization, and structural changes. Together, the development of advanced super-resolution microscopy, live-cell imaging, and biochemical approaches continues to refine our understanding of nuclear actin structure and dynamics.

Indexed as

ActinsCell FractionationCell NucleusAnimalsHumansActinsActinChromatinEpigenetic changesLaminNuclear isolation

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.