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

Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure.

Human reproduction (Oxford, England) - 1 Dec 2006

Westerveld G H, Korver C M, van Pelt A M M, Leschot N J, van der Veen F, Repping S, Lombardi M P

Abstract excerpt

BACKGROUND: Because of the common use of ICSI and the potential genetic aetiology of spermatogenic failure, concern has been raised about transmitting genetic disorders to ICSI offspring. However, to date, in only approximately 15% of all cases of spermatogenic failure, an underlying genetic cause can be identified. We have previously established an association between spermatogenic failure and chromosomal region...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Chromosomes, Human, Y

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomic Imprinting

Share to Infertility, Male

Share to Molecular Sequence Data

Share to Spermatogenesis

Share to Testis

Share to Tissue Distribution

Source

Identifiers

PMID: 16931801
DOI: 10.1093/humrep/del293

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

Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure.PMID 16931801Read ↗

Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failureSemantic proximity Read ↗

Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure.Semantic proximity Read ↗

Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.Semantic proximity Read ↗

Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.Semantic proximity Read ↗

Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.Semantic proximity Read ↗

Genetic variants in TEX15 gene conferred susceptibility to spermatogenic failure in the Chinese Han population.Semantic proximity Read ↗

BNC1 Promotes Spermatogenesis by Regulating Transcription of Ybx2 and Papolb via Direct Binding to Their Promotor Elements.Semantic proximity Read ↗

Spermatogenic phenotype of testis-specific protein, Y-encoded, 1 (TSPY1) dosage deficiency is independent of variations in TSPY-like 1 (TSPYL1) and TSPY-like 5 (TSPYL5): a case-control study in a Han Chinese population.Semantic proximity Read ↗

Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.Semantic proximity Read ↗

High Throughput Sequencing Identifies Misregulated Genes in the Drosophila Polypyrimidine Tract-Binding Protein (hephaestus) Mutant Defective in Spermatogenesis.Semantic proximity Read ↗

UTP14c is a recently acquired retrogene associated with spermatogenesis and fertility in man.Semantic proximity Read ↗

Chromosomal region 11p15 is associated with male factor subfertility.Semantic proximity Read ↗

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