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

SYCP3 mutations are uncommon in patients with azoospermia.

Fertility and sterility - 1 Oct 2005

Stouffs Katrien, Lissens Willy, Tournaye Herman, Van Steirteghem André, Liebaers Inge

Abstract excerpt

Mutation analysis of the SYCP3 gene was performed for 58 patients with a maturation arrest of spermatogenesis. In contrast to the previously reported high frequency of mutations, only polymorphisms were found in the present study.

Read the complete abstract on PubMed

Topics

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

Share to Cell Cycle Proteins
Share to DNA-Binding Proteins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nuclear Proteins

Share to Oligospermia

Source

Identifiers

PMID: 16213863
DOI: 10.1016/j.fertnstert.2005.04.033

Genes

SYCP3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SYCP3 mutations are uncommon in patients with azoospermia.PMID 16213863Read ↗

Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages.Semantic proximity Read ↗

Mutations of SYCP3 are rare in infertile Spanish men with meiotic arrest.Semantic proximity Read ↗

Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population.Semantic proximity Read ↗

A homozygous frameshift variant in SYCP2 caused meiotic arrest and non-obstructive azoospermia.Semantic proximity Read ↗

Analysis of STAG3 Mutations in Chinese Non-Obstructive Azoospermia Patients with Germ Cell Maturation ArrestSemantic proximity Read ↗

Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest.Semantic proximity Read ↗

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men.Semantic proximity Read ↗

Azoospermia in patients heterozygous for a mutation in SYCP3.Semantic proximity Read ↗

SIN3A mutations are rare in men with azoospermia.Semantic proximity Read ↗

Dicentric Y chromosome in an azoospermic maleSemantic proximity Read ↗

Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest.Semantic proximity Read ↗

Single nucleotide polymorphisms of USP26 in azoospermic men.Semantic proximity Read ↗

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