Evidence map›Paper›PMID 23779110›Full record

ReviewThe Journal of biological chemistry2013

Biological implications and regulatory mechanisms of long-range chromosomal interactions.

Zong Wei, David Huang, Fan Gao, Wen-Hsuan Chang, Woojin An, Gerhard A Coetzee, Kai Wang, Wange Lu

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  4. 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

8 authors.

Zong WeiEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, California 90033, USA.
David Huang
Fan Gao
Wen-Hsuan Chang
Woojin An
Gerhard A Coetzee
Kai Wang
Wange Lu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of high-throughput sequencing-based methods has enabled us to examine nuclear architecture at unprecedented resolution, allowing further examination of the function of long-range chromosomal interactions. Here, we review methods used to investigate novel long-range chromosomal interactions and genome-wide organization of chromatin. We further discuss transcriptional activation and silencing in relation to organization and positioning of gene loci and regulation of chromatin organization through protein complexes and noncoding RNAs.

Indexed as

Chromosomes, HumanCell NucleusGenome, HumanHigh-Throughput Screening AssaysHumansIn Situ Hybridization, FluorescenceLaminsPluripotent Stem CellsTranscription, GeneticTranslocation, GeneticX Chromosome InactivationLaminsChromatinChromatin RegulationChromatin StructureChromosome Conformation CaptureNuclear OrganizationNuclear Structure

Identifiers

PMID23779110
PMCPMC3829327

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.