ReviewCell biology international2026
Probing Centromere Plasticity and Chromatin Remodeling Using Single-Molecule Techniques.
Review in Cell biology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Probing Centromere Plasticity and Chromatin Remodeling Using Single-Molecule Techniques.Cell biology international · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
The centromere functions as an essential interactive hub for mediating the equal distribution of sister chromatids during eukaryotic cell division and is subject to cell cycle-specific plasticity regulation. To ensure the replication, transcription, and repair of genetic information, chromatin remodeling is an indispensable molecular biology event. Both centromere plasticity and chromatin remodeling involve numerous protein components (e.g., Constitutive Centromere-Associated Network (CCAN), SWItch/Sucrose Non-Fermentable (SWI/SNF)) and exhibit highly dynamic spatiotemporal regulation, posing significant challenges for traditional ensemble approaches in elucidating their detailed mechanisms. In recent years, single-molecule techniques have revolutionized the study of chromatin remodeling and kinetochore assembly. By capturing real-time, high-resolution dynamics of molecular interactions, these methods uncover mechanistic insights inaccessible to conventional approaches. This review summarizes key advances and emerging paradigms enabled by single-molecule analysis tools, highlighting how they are reshaping our understanding of the mechanism of mitotic fidelity and epigenetic regulation, and providing a roadmap for future research in these fields.
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What OpenQuestion holds
Registered trials
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.