Evidence map›Paper›PMID 22343041›Full record

ArticleMethods (San Diego, Calif.)2012

Experimental approaches to identify cellular G-quadruplex structures and functions.

Marco Di Antonio, Raphaël Rodriguez, Shankar Balasubramanian

Open access · hybridAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  5. Modulation of DNA structure formation using small molecules.Biochimica et biophysica acta. Molecular cell research · 2019
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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

3 authors at 1 institution in 1 country.

Marco Di AntonioUniversity of Cambridge, Department of Chemistry, Lensfield Road, Cambridge CB2 1EW, UK.
Raphaël Rodriguez
Shankar Balasubramanian
University of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G008337/1Cancer Research UK 11961
6 · The paper itself

Abstract

Guanine-rich nucleic acids can fold into non-canonical DNA secondary structures called G-quadruplexes. The formation of these structures can interfere with the biology that is crucial to sustain cellular homeostases and metabolism via mechanisms that include transcription, translation, splicing, telomere maintenance and DNA recombination. Thus, due to their implication in several biological processes and possible role promoting genomic instability, G-quadruplex forming sequences have emerged as potential therapeutic targets. There has been a growing interest in the development of synthetic molecules and biomolecules for sensing G-quadruplex structures in cellular DNA. In this review, we summarise and discuss recent methods developed for cellular imaging of G-quadruplexes, and the application of experimental genomic approaches to detect G-quadruplexes throughout genomic DNA. In particular, we will discuss the use of engineered small molecules and natural proteins to enable pull-down, ChIP-Seq, ChIP-chip and fluorescence imaging of G-quadruplex structures in cellular DNA.

Indexed as

G-QuadruplexesNucleic Acid ConformationCircular DichroismDNAGuanineKineticsLigandsOligonucleotidesSolutionsTelomereThermodynamicsWaterDNAGuanineLigandsOligonucleotidesSolutionsWater

Identifiers

PMID22343041
PMCPMC3563962
OpenAlexW2075747958

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.