Evidence map›Paper›PMID 30469382›Full record

ReviewGenes2018

Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11.

Francesca M Pisani, Ettore Napolitano, Luisa M R Napolitano, Silvia Onesti

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  16. Article
  17. Spotlight on Warsaw Breakage Syndrome.The application of clinical genetics · 2019
    Review
  18. The Role of UpregulatedJournal of Cancer · 2019
    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

4 authors at 2 institutions in 1 country.

Francesca M PisaniIstituto di Biochimica delle Proteine, Consiglio Nazionale delle Ricerche, Via P. Castellino, 111, 80131 Napoli, Italy. fm.pisani@ibp.cnr.it.ORCID 0000-0002-4591-7571
Ettore NapolitanoIstituto di Biochimica delle Proteine, Consiglio Nazionale delle Ricerche, Via P. Castellino, 111, 80131 Napoli, Italy. e.napolitano@ibp.cnr.it.ORCID 0000-0001-6160-1860
Luisa M R NapolitanoElettra⁻Sincrotrone Trieste S.C.p.A., AREA Science Park Basovizza, 34149 Trieste, Italy. luisa.napolitano@elettra.eu.
Silvia OnestiElettra⁻Sincrotrone Trieste S.C.p.A., AREA Science Park Basovizza, 34149 Trieste, Italy. silvia.onesti@elettra.eu.ORCID 0000-0002-0612-7948
Elettra-Sincrotrone Trieste S.C.p.A. · ITInstitute of Protein Biochemistry · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG 20778Cross-Border Cooperation Programme Italy-Slovenia 2014-2020 by the European Regional Development Fund and national funds TransGlioma
6 · The paper itself

Abstract

DDX11/ChlR1 (Chl1 in yeast) is a DNA helicase involved in sister chromatid cohesion and in DNA repair pathways. The protein belongs to the family of the iron⁻sulphur cluster containing DNA helicases, whose deficiencies have been linked to a number of diseases affecting genome stability. Mutations of human DDX11 are indeed associated with the rare genetic disorder named Warsaw breakage syndrome, showing both chromosomal breakages and chromatid cohesion defects. Moreover, growing evidence of a potential role in oncogenesis further emphasizes the clinical relevance of DDX11. Here, we illustrate the biochemical and structural features of DDX11 and how it cooperates with multiple protein partners in the cell, acting at the interface of DNA replication/repair/recombination and sister chromatid cohesion to preserve genome stability.

Indexed as

DDX11DNA helicaseDNA repair/recombinationDNA replicationgenome stability maintenanceiron-sulphur clustersister chromatid cohesionWarsaw breakage syndrome

Identifiers

PMID30469382
PMCPMC6266566
OpenAlexW2901819144

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.