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

Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure†

7 Feb 2017

Abstract excerpt

Spermatogenic failure characterized by impaired sperm production is a common multifactorial disease with molecular and cytogenetic causes for its extreme phenotype that include azoospermia and severe oliogzoospermia. Recently, a high-resolution array-comparative genomic hybridization analysis of the X chromosome and a subsequent cohort study revealed three X-linked microdeletions (CNV64, CNV67, and CNV69) that...

Read the complete abstract on PubMed

Topics

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

Share to Animal Genetics and Reproduction
Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sperm and Testicular Function

Source

Identifiers

PMID: 28339631
DOI: 10.1093/biolre/iox006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure†PMID 28339631Read ↗

Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.Semantic proximity Read ↗

Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertilitySemantic proximity Read ↗

Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermiaSemantic proximity Read ↗

Utility of exome sequencing in primary spermatogenic disorders: From research to diagnosticsSemantic proximity Read ↗

DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermiaSemantic proximity Read ↗

High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.Semantic proximity Read ↗

Genetic pathogenesis of acephalic spermatozoa syndrome: past, present, and future.Semantic proximity Read ↗

Identification and functional analysis of spermatogenesis‐associated gene modules in azoospermia by weighted gene coexpression network analysisSemantic proximity Read ↗

Analysis of genomic copy number variation in 48 azoospermia patients with chromosomal abnormalitiesSemantic proximity Read ↗

<p>Deficient Expression of <em>DGCR8</em> in Human Testis is Related to Spermatogenesis Dysfunction, Especially in Meiosis I</p>Semantic proximity Read ↗

Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure.Semantic proximity Read ↗

Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Semantic proximity Read ↗

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