Evidence map›Paper›PMID 30420415›Full record

ReviewBiochemical Society transactions2018

PARPs in genome stability and signal transduction: implications for cancer therapy.

Luca Palazzo, Ivan Ahel

Open access · hybridAbstract readReview
In one paragraph

Review in Biochemical Society transactions, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.2field-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

39 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
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  15. High Expression ofFrontiers in oncology · 2022
    Article
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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

2 authors at 2 institutions in 2 countries.

Luca PalazzoInstitute of Protein Biochemistry, National Research Council, Via Pietro Castellino 111, 80131 Naples, Italy l.palazzo@ibp.cnr.it ivan.ahel@path.ox.ac.uk.ORCID 0000-0002-5556-5549
Ivan AhelSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, U.K. l.palazzo@ibp.cnr.it ivan.ahel@path.ox.ac.uk.ORCID 0000-0002-9446-3756
Institute of Protein Biochemistry · ITUniversity of Oxford · GB

Funding

Cancer Research UK 22284Cancer Research UK C35050/A22284European Research Council 281739Wellcome Trust 101794
6 · The paper itself

Abstract

The poly(ADP-ribose) polymerase (PARP) superfamily of enzymes catalyses the ADP-ribosylation (ADPr) of target proteins by using nicotinamide adenine dinucleotide (NAD

Indexed as

Adenosine Diphosphate RiboseAnimalsDNA DamageGenomic InstabilityHumansNeoplasmsPoly(ADP-ribose) PolymerasesAdenosine Diphosphate RibosePoly(ADP-ribose) Polymerasesadenosine diphosphate ribosecancerDNA damage responsePARPssignalling

Identifiers

PMID30420415
PMCPMC6299239
OpenAlexW2900584308

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.