Evidence map›Paper›PMID 36816512›Full record

ArticleFASEB bioAdvances2023

Cell migration is impaired in XPA-deficient cells.

Seiji Takeuchi, Takeshi Fukumoto, Chihiro Takemori, Naoaki Saito, Chikako Nishigori, Makoto Sato

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in FASEB bioAdvances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. DNA damage and repair: underlying mechanisms leading to microcephaly.Frontiers in cell and developmental biology · 2023
    Review
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

6 authors at 3 institutions in 1 country.

Seiji TakeuchiDivision of Dermatology, Department of Internal Related Kobe University Graduate School of Medicine Kobe Japan.
Takeshi FukumotoDivision of Dermatology, Department of Internal Related Kobe University Graduate School of Medicine Kobe Japan.ORCID https://orcid.org/0000-0003-0364-711X
Chihiro TakemoriDivision of Dermatology, Department of Internal Related Kobe University Graduate School of Medicine Kobe Japan.
Naoaki SaitoLaboratory of Molecular Pharmacology, Biosignal Research Center Kobe University Kobe Japan.
Chikako NishigoriDivision of Dermatology, Department of Internal Related Kobe University Graduate School of Medicine Kobe Japan.
Makoto SatoDivision of Cell Biology and Neuroscience Department of Morphological and Physiological Sciences, Faculty of Medical Sciences University of Fukui Fukui Japan.ORCID https://orcid.org/0000-0002-6805-8351
Kobe University · JPKanazawa University · JPUniversity of Fukui · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xeroderma pigmentosum (XP) is a hereditary disorder characterized by photosensitivity, predisposition to skin cancers, and neurological abnormalities including microcephaly and progressive neurodegeneration. A lack of nucleotide excision repair (NER) in patients with XP can cause hypersensitivity to the sun, leading to skin cancer, whereas the etiology of the neuronal symptoms of XP remains ambiguous. There are various neurological disorders that perturb neuronal migration, causing mislocalization and disorganization of the cortical lamination. Here, we investigated the role of the XP group-A (

Identifiers

PMID36816512
PMCPMC9927838
OpenAlexW4309573047

What Socratic 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 Socratic graph.