Evidence map›Paper›PMID 42681054›Full record

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

Studying Cell Wall-Associated Effectors in U. maydis.

Shigeyuki Tanaka

Abstract read
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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

1 author.

Shigeyuki TanakaFaculty of Agriculture, Setsunan University, 45-1 Nagaotoge-cho, Hirakata, Osaka, 573-0101, Japan. shigeyuki.tanaka@setsunan.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fungal cell wall-binding secreted effector proteins play pivotal roles in plant-microbe interactions and cell wall remodeling in Ustilago maydis. Accurate assessment of their localization and binding mode is essential for understanding their biological function. Here, a protocol combining immunolocalization with fluorescence microscopy and immunoprecipitation (IP) under both native and denaturing (SDS-containing) conditions is described. Immunolocalization provides direct visualization of protein distribution at the cell wall, while comparative IP experiments reveal the strength and nature of protein-cell wall associations. This combined approach offers a reproducible and adaptable framework for analyzing secreted proteins that associate with cell walls.

Indexed as

Cell WallFungal ProteinsUstilagoBasidiomycotaImmunohistochemistryImmunoprecipitationMicroscopy, FluorescenceFungal ProteinsEffector proteinsFluorescent microscopyFungal cell wallImmunocytochemistryImmunoprecipitation

Identifiers

What OpenQuestion holds

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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.