Evidence map›Paper›PMID 28367085›Full record

ArticleInternational journal of medical sciences2017

Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene.

Swee-Hee Wong, Wen-Hung Wang, Pin-Hua Chen, Shuan-Yow Li, Jiann-Jou Yang

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

Article in International journal of medical sciences, 2017. 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
0.3field-weighted citation impact, top 41% 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, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Experimental biology and medicine (Maywood, N.J.) · 2020
    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

5 authors at 3 institutions in 1 country.

Swee-Hee WongDepartment of BioMedical Sciences, Chung Shan Medical University, Taichung, Taiwan;; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Wen-Hung WangDepartment of Otolaryngology, Cathay General Hospital, Taipei, Taiwan.
Pin-Hua ChenDepartment of BioMedical Sciences, Chung Shan Medical University, Taichung, Taiwan.
Shuan-Yow LiDepartment of BioMedical Sciences, Chung Shan Medical University, Taichung, Taiwan;; Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.
Jiann-Jou YangDepartment of BioMedical Sciences, Chung Shan Medical University, Taichung, Taiwan;; Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.
Chung Shan Medical University · TWChung Shan Medical University Hospital · TWCathay General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In a previous study, we identified a novel missense mutation, p.W77S, in the

Indexed as

Structure-Activity RelationshipConnexinsDeafnessEndoplasmic ReticulumGap JunctionsGene Expression RegulationHeLa CellsHumansLysosomesMutation, MissenseNerve Tissue ProteinsProtein DomainsProteolysisConnexinsGJC3 protein, humanNerve Tissue ProteinsCX30.2/CX31.3GJC3hearing loss.mutation

Identifiers

PMID28367085
PMCPMC5370287
OpenAlexW2593612234

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.