Evidence map›Paper›PMID 42642605›Full record

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

MicroRNA Extraction from Extracellular Vesicles by Nanowire Devices.

Taiga Ajiri, Kunanon Chattrairat, Takao Yasui

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.

Taiga AjiriNagoya University, Nagoya, Aichi, Japan.
Kunanon ChattrairatNagoya University, Nagoya, Aichi, Japan.
Takao YasuiNagoya University, Nagoya, Aichi, Japan. yasui@chembio.nagoya-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) are membrane-bound particles secreted by various cell types; EVs are found abundantly in body fluids, and they play significant roles in intercellular communication. Among the molecules contained in EVs, microRNAs are key regulators of gene expression, and they have been implicated in numerous diseases, including neurodegenerative disorders and cancers. Conventional methods for miRNA analysis, such as ultracentrifugation and immunoaffinity-based techniques, face challenges including the need for large sample volumes and low yield efficiency. To address these issues, our group has developed two types of innovative nanowire devices (inorganic nanowires composed of zinc oxide (ZnO) and organic nanowires composed of cellulose nanofibers) for the efficient capture and analysis of EV-derived miRNAs. In this chapter, we introduce the procedures for fabricating our inorganic and organic nanowire devices, as well as the methods for analyzing miRNAs extracted from EVs using the fabricated devices.

Indexed as

Extracellular VesiclesMicroRNAsNanowiresCelluloseHumansLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesZinc OxideCelluloseMicroRNAsZinc OxideCellulose nano fiberExtracellular vesiclesMicrofluidic deviceMicroRNAsNano deviceNanowire

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.