Evidence map›Paper›PMID 26221352›Full record

ArticleInternational journal of clinical and experimental medicine2015

Association of polymorphisms in ART3 gene with male infertility in the Chinese population.

Feiyan Lin, Lei Jiang, Haiyan Yang, Xu Yang, Jianbo Wu, Xuefeng Huang, Wuhua Ni

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Feiyan LinLaboratory of Internal Medicine, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Lei JiangLaboratory of Internal Medicine, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Haiyan YangReproductive Medicine Center, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Xu YangReproductive Medicine Center, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Jianbo WuLaboratory of Internal Medicine, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Xuefeng HuangReproductive Medicine Center, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Wuhua NiReproductive Medicine Center, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ADP-ribosyltransferase 3 gene (ART3) has been reported to be associated with non-obstructive azoospermia (NOA) in the Japanese population. In this study, we aim to explore the possible association between the four single nucleotide polymorphisms (SNPs) (rs11097230, rs17001385, rs14773 and rs6836703) in ART3 gene and male infertility with spermatogenesis impairment in the Chinese population. The study population included 321 idiopathic infertile males with azoospermia or oligozoospermia and 250 fertile males. Four SNPs of ART3 gene were genotyped using the method of SNaPshot. The results showed that an SNP (rs6836703) in the intron11 region of ART3 gene is significantly associated with male infertility (odds ratio: 0.632, 95% confidence interval: 0.440-0.910). No significant associations were found between any of the other three variants (rs11097230, rs17001385 and rs14773) in ART3 gene and male infertility. SNP rs6836703 in ART3 gene may contribute to male infertility risk in the Chinese population.

Indexed as

ART3Chinese populationgenegenotypemale infertilitysingle nucleotide polymorphisms

Identifiers

PMID26221352
PMCPMC4509297
OpenAlexW2414633744

What OpenQuestion holds

Textmetadata
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.