Evidence map›Paper›PMID 24817005›Full record

ArticleJournal of assisted reproduction and genetics2014

Association of MOV10L1 gene polymorphisms and male infertility in azoospermic men with complete maturation arrest.

Homa Sarkardeh, Mehdi Totonchi, Ommolbanin Asadpour, Mohammad Ali Sadighi Gilani, Masoud Zamani Esteki, Navid Almadani, Parnaz Borjian Boroujeni, Hamid Gourabi

Open access · bronzeAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. A novel missense variant inJournal of genetics · 2024
    Article
  3. Article
  4. Review
  5. Coding and Non-Coding RNAs, as Male Fertility and Infertility Biomarkers.International journal of fertility & sterility · 2021
    Review
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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

8 authors at 3 institutions in 2 countries.

Homa SarkardehDepartment of Genetics at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, P.O. Box 19395-4644, Tehran, Iran.
Mehdi Totonchi
Ommolbanin Asadpour
Mohammad Ali Sadighi Gilani
Masoud Zamani Esteki
Navid Almadani
Parnaz Borjian Boroujeni
Hamid Gourabi
Royan Institute · IRAcademic Center for Education, Culture and Research · IRKU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe present research was undertaken to study probable genetic variations of MOV10L1 in 30 infertile men that had complete maturation arrest in their spermatocyte levels and 70 fertile men as the control group.

methodsWe performed polymerase chain reaction single strand conformation polymorphism (PCR-SSCP) on extracted DNAs and sequencing was used to confirm the results. Identified polymorphisms in the MOV10L1 were further subjected to a haplotype analysis.

resultsWe identified eight single nucleotide polymorphisms (SNPs): one missense (rs2272837) and four nonsense polymorphisms (rs2272836, rs11704548, rs2272838, rs138271) in the exonic sequences and three polymorphisms (rs12170772, rs2272840, rs17248147) in the intronic regions. With the exception of rs2272838, there was a statistically significant association in all polymorphisms between study population (P < 0.05). The result of haplotyping analysis showed ten possible haplotypes, from which five were significantly increased in infertile patients compared with the control group.

conclusionsOur results suggest that MOV10L1 gene polymorphisms in the studied infertile males with complete maturation arrest are linked to infertility.

Indexed as

Genetic Predisposition to DiseaseAdultAllelesAzoospermiaGenetic Association StudiesHaplotypesHumansInfertility, MaleIranMaleOligospermiaPolymorphism, Single NucleotideRNA HelicasesRNA, Small InterferingMov10 protein, humanRNA HelicasesRNA, Small Interfering

Identifiers

PMID24817005
PMCPMC4096888
OpenAlexW2156835016

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.