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

Lack of association of KATNAL1 gene sequence variants and azoospermia in humans.

Journal of assisted reproduction and genetics - 1 Aug 2014

Fedick Anastasia M, Eckert Kyle, Thompson Katharine, Forman Eric J, Devkota Batsal, Treff Nathan R, Taylor Deanne, Scott Richard T

Abstract excerpt

PURPOSE: A recent experiment indicated that a loss of function mutation in the murine Katnal1 gene resulted in male factor infertility due to premature exfoliation of spermatids. This study investigated the relevance of this gene to infertility in humans. METHODS: Multiple methods of genetic anal...

Read the complete abstract on PubMed

Topics

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

Share to Azoospermia
Share to Case-Control Studies
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Endopeptidases

Share to Haplotypes

Share to Infertility, Male

Share to Polymorphism, Single Nucleotide

Share to Semen Analysis

Source

Open in PubMed Open full text

Identifiers

PMID: 24913027
DOI: 10.1007/s10815-014-0269-1
PMCID: PMC4130932

Genes

KATNAL1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24913027-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lack of association of KATNAL1 gene sequence variants and azoospermia in humans.PMID 24913027Read ↗

Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.Semantic proximity Read ↗

Targeted Next-Generation Sequencing Identifies Novel Sequence Variations of Genes Associated with Nonobstructive Azoospermia in the Han Population of Northeast ChinaSemantic proximity Read ↗

Analysis of copy number variation in men with non‐obstructive azoospermiaSemantic proximity Read ↗

KATNB1 in the human testis and its genetic variants in fertile and oligoasthenoteratozoospermic infertile men.Semantic proximity Read ↗

Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermiaSemantic proximity Read ↗

Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese men.Semantic proximity Read ↗

The PGAM4 gene in non-obstructive azoospermia.Semantic proximity Read ↗

The TNP1 haplotype - GCG is associated with azoospermia.Semantic proximity Read ↗

MBOAT1 homozygous missense variant causes nonobstructive azoospermia.Semantic proximity Read ↗

Association of CLCA4 genetic variation with non-obstructive azoospermia and its potential interaction with Y-chromosome microdeletions.Semantic proximity Read ↗

Mutational analysis of the GATA4 gene in Chinese men with nonobstructive azoospermia.Semantic proximity Read ↗

Genomic and genetic variation in E2F transcription factor-1 in men with nonobstructive azoospermia.Semantic proximity Read ↗

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