Evidence map›Paper›PMID 40740627›Full record

ArticleJournal of human reproductive sciences

Novel SUN5 Mutation Associated with Acephalic Spermatozoa Syndrome: A Cross-sectional Study.

Sarvenaz Alinia, Fatemeh Eskandari Chenari, Seyedeh-Hanieh Hosseini, Alemeh Rafaee, Amaneh Javid, Mohammad Ali Sadighi Gilani, Marjan Sabbaghian

Abstract read
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Article in Journal of human reproductive sciences. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Sarvenaz AliniaDepartment of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Fatemeh Eskandari ChenariDepartment of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Seyedeh-Hanieh HosseiniDepartment of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Alemeh RafaeeDepartment of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Amaneh JavidDepartment of Biological Sciences, Faculty of Engineering and Science, Science and Arts University, Yazd, Iran.
Mohammad Ali Sadighi GilaniDepartment of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Marjan SabbaghianDepartment of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Aim: This study aims to evaluate the genetic variants of all exons of the Settings and Design: This cross-sectional study was conducted on 10 infertile men with ASS as a case group and 10 men with normal spermogram as a control group referred to the Royan institute between 2015 and 2020. Materials and Methods: Polymerase chain reaction and Sanger sequencing were performed on DNA extracted from patients' peripheral blood. In addition, immunocytochemistry and western blotting were accomplished to evaluate the SUN5 protein expression in the patient carrying a distinct exonic variation. Statistical Analysis Used: No statistical analysis was needed to be done in this survey. Results: Sequencing outcomes represented one homozygous missense mutation (c.1073G>A [p.Arg358Gln]) in exon 13 of the Conclusion: Based on current results, it could be concluded that c.1073G>A detected mutations in the

Indexed as

Acephalic spermatozoa syndromemale infertilitymutationSUN5 gene

Identifiers

PMID40740627
PMCPMC12306721

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