Evidence map›Paper›PMID 32163217›Full record

ArticleAngewandte Chemie (International ed. in English)2020

A Small-Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies.

Ming-Yu Wu, Jong-Kai Leung, Li Liu, Chuen Kam, Kelvin Yuen Kwong Chan, Ronald A Li, Shun Feng, Sijie Chen

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. A near-infrared AIE fluorescent probe for myelin imaging: From sciatic nerve to the optically cleared brain tissue in 3D.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Article
  5. A Small-Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies.Angewandte Chemie (International ed. in English) · 2020
    Article
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

8 authors.

Ming-Yu WuMing Wai Lau Centre for Reparative Medicine, Karolinska Institutet, Hong Kong, China.ORCID 0000-0002-2047-3441
Jong-Kai LeungMing Wai Lau Centre for Reparative Medicine, Karolinska Institutet, Hong Kong, China.ORCID 0000-0002-1452-3473
Li LiuSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, 610031, China.
Chuen KamMing Wai Lau Centre for Reparative Medicine, Karolinska Institutet, Hong Kong, China.
Kelvin Yuen Kwong ChanDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, China.
Ronald A LiMing Wai Lau Centre for Reparative Medicine, Karolinska Institutet, Hong Kong, China.ORCID 0000-0002-2980-5019
Shun FengSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, 610031, China.ORCID 0000-0003-1602-0244
Sijie ChenMing Wai Lau Centre for Reparative Medicine, Karolinska Institutet, Hong Kong, China.ORCID 0000-0001-5263-9189

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chromosome periphery (CP) is a complex network that covers the outer surface of chromosomes. It acts as a carrier of nucleolar components, helps maintain chromosome structure, and plays an important role in mitosis. Current methods for fluorescence imaging of CP largely rely on immunostaining. We herein report a small-molecule fluorescent probe, ID-IQ, which possesses aggregation-induced emission (AIE) property, for CP imaging. By labelling the CP, ID-IQ sharply highlighted the chromosome boundaries, which enabled rapid segmentation of touching and overlapping chromosomes, direct identification of the centromere, and clear visualization of chromosome morphology. ID-IQ staining was also compatible with fluorescence in situ hybridization and could assist the precise location of the gene in designated chromosome. Altogether, this study provides a versatile cytogenetic tool for improved chromosome analysis, which greatly benefits the clinical diagnostic testing and genomic research.

Indexed as

CarbolinesCell Line, TumorCentromereChromosomesCytogenetic AnalysisFluorescent DyesHumansInduced Pluripotent Stem CellsIn Situ Hybridization, FluorescenceLymphocytesMicroscopy, ConfocalMicroscopy, FluorescenceCarbolinesFluorescent Dyesaggregation-induced emissioncentromereschromosome analysischromosome peripheryfluorescence imaging

Identifiers

PMID32163217
PMCPMC7318220

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Registered trials

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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.