Evidence map›Paper›PMID 30658521›Full record

ArticleGenes2019

Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders.

Maria Marín, María José Ramírez, Miriam Aza Carmona, Nan Jia, Tomoo Ogi, Massimo Bogliolo, Jordi Surrallés

Open access · goldAbstract read
In one paragraph

Article in Genes, 2019. 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
0.9field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Maria MarínDepartament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, 08028 Barcelona, Spain. mariamarinvilar@gmail.com.
María José RamírezDepartament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, 08028 Barcelona, Spain. mariajose.ramirez@uab.cat.
Miriam Aza CarmonaDepartament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, 08028 Barcelona, Spain. miriam.azacarmona@gmail.com.
Nan JiaDepartment of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Nagoya, Japan/Department of Human Genetics and Molecular Biology, Graduate School of Medicine, Nagoya University, Nagoya 464-0805, Japan. jia.nan@riem.nagoya-u.ac.jp.
Tomoo OgiDepartment of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Nagoya, Japan/Department of Human Genetics and Molecular Biology, Graduate School of Medicine, Nagoya University, Nagoya 464-0805, Japan. togi@riem.nagoya-u.ac.jp.
Massimo BoglioloDepartament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, 08028 Barcelona, Spain. massimo.bogliolo@uab.cat.
Jordi SurrallésDepartament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, 08028 Barcelona, Spain. jsurralles@santpau.cat.ORCID 0000-0002-4041-7519
Universitat Autònoma de Barcelona · ESNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

XPF endonuclease is one of the most important DNA repair proteins. Encoded by

Indexed as

Mutation, MissensePhenotypeDNA-Binding ProteinsDNA RepairDNA Repair-Deficiency DisordersHEK293 CellsHumansProtein StabilityRadiation ToleranceDNA-Binding Proteinsxeroderma pigmentosum group F proteinDNA repairgenotype-phenotype correlationXPF/ERCC4 mutationsXPF-KO

Identifiers

PMID30658521
PMCPMC6357085
OpenAlexW2910053627

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.