Evidence map›Paper›PMID 28688039›Full record

ReviewChromosoma2017

Using human artificial chromosomes to study centromere assembly and function.

Oscar Molina, Natalay Kouprina, Hiroshi Masumoto, Vladimir Larionov, William C Earnshaw

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Chromosoma, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
9.1field-weighted citation impact, top 3% of its field
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

20 citing papers in PubMed, 25 citations in OpenAlex.

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  13. TAR Cloning: Perspectives for Functional Genomics, Biomedicine, and Biotechnology.Molecular therapy. Methods & clinical development · 2019
    Review
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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

5 authors at 4 institutions in 4 countries.

Oscar MolinaWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, EH9 3QR, UK. omolina@carrerasresearch.org.ORCID http://orcid.org/0000-0001-7585-4519
Natalay KouprinaGenome Structure and Function group, Developmental Therapeutics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Hiroshi MasumotoLaboratory of Cell Engineering. Department of Frontier Research, Kazusa DNA Research Institute, Kisarazu, 292-0818, Japan.
Vladimir LarionovGenome Structure and Function group, Developmental Therapeutics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
William C EarnshawWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, EH9 3QR, UK. bill.earnshaw@ed.ac.uk.ORCID http://orcid.org/0000-0002-7191-0621
National Institutes of Health · USJosep Carreras Leukaemia Research Institute · ESKazusa DNA Research Institute · JPWellcome Centre for Cell Biology · GB

Funding

Study of hereditary prostate cancer and human artificial chromosomesZIABC010413 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARIONOV, VLADIMIR · 2009 to 2025
$31.5M
European Molecular Biology Organization ALTF-453-2012MEXT KAKENHI 23114008MEXT KAKENHI 23247030Wellcome Trust 073915
6 · The paper itself

Abstract

Centromeres are the site of assembly of the kinetochore, which directs chromosome segregation during cell division. Active centromeres are characterized by the presence of nucleosomes containing CENP-A and a specific chromatin environment that resembles that of active genes. Recent work using human artificial chromosomes (HAC) sheds light on the fine balance of different histone post-translational modifications and transcription that exists at centromeres for kinetochore assembly and maintenance. Here, we review the use of HAC technology to understand centromere assembly and function. We put particular emphasis on studies using the alphoid

Indexed as

Chromatin Assembly and DisassemblyChromosomes, Artificial, HumanGenetic TechniquesCentromereEpigenesis, GeneticHumansCENP-ACentromereHuman artificial chromosomesKinetochoreMitosis

Identifiers

PMID28688039
OpenAlexW2731919256

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.