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

A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia

19 Apr 2016

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Sexual Differentiation and Disorders
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 27089915
DOI: 10.1177/1933719116641758

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive AzoospermiaPMID 27089915Read ↗

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

Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.Semantic proximity Read ↗

Novel mutations in testis-specific ubiquitin protease 26 gene may cause male infertility and hypogonadism.Semantic proximity Read ↗

Ubiquitin-specific protease (USP26) gene alterations associated with male infertility and recurrent pregnancy loss (RPL) in Iranian infertile patients.Semantic proximity Read ↗

Association of 370-371insACA, 494T>C, and 1423C>T haplotype in ubiquitin-specific protease 26 gene and male infertility: a meta-analysis.Semantic proximity Read ↗

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y.Semantic proximity Read ↗

Alterations of the USP26 gene in Caucasian men.Semantic proximity Read ↗

Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility.Semantic proximity Read ↗

The association between mutations in ubiquitin-specific protease 26 (USP26) and male infertility: a systematic review and meta-analysis.Semantic proximity Read ↗

[Polymorphism of Usp26 correlates with idiopathic male infertility].Semantic proximity Read ↗

Possible role of USP26 in patients with severely impaired spermatogenesis.Semantic proximity Read ↗

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferensSemantic proximity Read ↗

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