Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men.

Andrologia - 1 Dec 2020

Nasirshalal Mahzad, Tahmasebi-Birgani Maryam, Dadfar Mohammadreza, Nikbakht Roshan, Saberi Alihossein, Ghandil Pegah

Abstract excerpt

Mutations or altered expression of PRM1 gene have been associated with male infertility. This study aimed to analyse pathogenic variations of PRM1 gene in Iranian Arab infertile men with oligoasthenoteratozoospermia that was carried out for the first time in this population. Genomic DNA was used to perform PCR sequencing in PRM1 untranslated regions, exons and intron. Also, bioinformatics analysis was recruited...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Infertility, Male
Share to Iran
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Oligospermia

Share to Protamines

Source

Identifiers

PMID: 33118225
DOI: 10.1111/and.13872

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men.PMID 33118225Read ↗

Association of polymorphisms in PATE1 gene with idiopathic asthenozoospermia in Sichuan, China.Semantic proximity Read ↗

Genetic aspects of idiopathic asthenozoospermia as a cause of male infertilitySemantic proximity Read ↗

PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population.Semantic proximity Read ↗

The impact of RABL2B gene (rs144944885) on human male infertility in patients with oligoasthenoteratozoospermia and immotile short tail sperm defects.Semantic proximity Read ↗

A genome-wide association study of mitochondrial DNA in Chinese men identifies two risk single nucleotide substitutions for idiopathic oligoasthenospermia.Semantic proximity Read ↗

Integrated Analysis of DNA Methylation and mRNA Expression Profiles to Identify Key Genes in Severe OligozoospermiaSemantic proximity Read ↗

A novel frameshift mutation in DNAH6 associated with male infertility and asthenoteratozoospermiaSemantic proximity Read ↗

Splicing Mutation in DNALI1 Causes Male Infertility with Severe Oligoasthenoteratozoospermia in Humans.Semantic proximity Read ↗

Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia.Semantic proximity Read ↗

[Update of asthenospermia-related genes and proteins].Semantic proximity Read ↗

The c.-190 C>A transversion in promoter region of protamine1 gene as a genetic risk factor for idiopathic oligozoospermia.Semantic proximity Read ↗

DNA methylation patterns in patients with asthenospermia and oligoasthenospermiaSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.