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

The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.

Journal of assisted reproduction and genetics - 1 Nov 2011

Safinejad Kyumars, Darbouy Mojtaba, Kalantar Sayed Mahdi, Zeinali Sirus, Mirfakhraie Reza, Yadegar Leila, Houshmand Masoud

Abstract excerpt

PURPOSE: To evaluate five common cystic fibrosis trans-membrane conductance regulator (CFTR) mutations (ΔF508, G542X, R117H, W1282X and N1303K) in the Iranian infertile men with noncongenital absence of vas deferens (CAVD) obstructive azoospermia. METHODS: The common CFTR gene mutations were tested on blood samples from 53 infertile men with non-CAVD obstructive azoospermia and 50 normal men as control...

Read the complete abstract on PubMed

Topics

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

Share to Azoospermia
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Male Urogenital Diseases

Share to Nucleic Acid Amplification Techniques

Share to Prevalence

Share to Vas Deferens

Source

Open in PubMed Open full text

Identifiers

PMID: 21976147
DOI: 10.1007/s10815-011-9632-7
PMCID: PMC3224173

Genes

CFTR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.PMID 21976147Read ↗

A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian PopulationSemantic proximity Read ↗

Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure.Semantic proximity Read ↗

The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia.Semantic proximity Read ↗

Mutations in CFTR genes are associated with oligoasthenospermia in infertile men undergoing IVF.Semantic proximity Read ↗

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator mutations in azoospermic and oligospermic men and their partners.Semantic proximity Read ↗

Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.Semantic proximity Read ↗

Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.Semantic proximity Read ↗

[The detection of CFTR gene mutation in patients with azoospermia].Semantic proximity Read ↗

Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.Semantic proximity Read ↗

CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study.Semantic proximity Read ↗

An overview of CFTR mutation profiles and assisted reproductive technology outcomes in Chinese patients with congenital obstructive azoospermia.Semantic proximity Read ↗

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