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

Quantification of DDX3Y, RBMY1, DAZ and TSPY mRNAs in testes of patients with severe impairment of spermatogenesis

19 Sept 2007

Abstract excerpt

Y chromosome microdeletion is the most important genetic cause of impairment of spermatogenesis. Nevertheless, a significant proportion of patients with spermatogenic failure do not have this condition. This study investigated the expression level of AZF genes, DDX3Y (DBY), RBMY1, DAZ and TSPY in testicular tissues of 42 subjects with impaired spermatogenesis compared with 33 with normal spermatogenesis....

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: 17881721
DOI: 10.1093/molehr/gam057

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Quantification of DDX3Y, RBMY1, DAZ and TSPY mRNAs in testes of patients with severe impairment of spermatogenesisPMID 17881721Read ↗

Expression profile of AZF genes in testicular biopsies of azoospermic menSemantic proximity Read ↗

Isoform-Level Gene Expression Profiles of Human Y Chromosome Azoospermia Factor Genes and Their X Chromosome Paralogs in the Testicular Tissue of Non-Obstructive Azoospermia PatientsSemantic proximity Read ↗

AZFa protein DDX3Y is differentially expressed in human male germ cells during development and in testicular tumours: new evidence for phenotypic plasticity of germ cells.Semantic proximity Read ↗

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein geneSemantic proximity Read ↗

Y chromosome microdeletions and alterations of spermatogenesis.Semantic proximity Read ↗

Expression patterns and transcript concentrations of the autosomal DAZL gene in testes of azoospermic menSemantic proximity Read ↗

Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion.Semantic proximity Read ↗

AZF and DAZ gene copy-specific deletion analysis in maturation arrest and Sertoli cell-only syndromeSemantic proximity Read ↗

The AZFa gene DBY (DDX3Y) is widely transcribed but the protein is limited to the male germ cells by translation controlSemantic proximity Read ↗

Y-chromosome microdeletion and phenotype in cytogenetically normal men with idiopathic azoospermia.Semantic proximity Read ↗

Characterization of DDX4 Gene Expression in Human Cases with Non-Obstructive Azoospermia and in Sterile and Fertile MiceSemantic proximity Read ↗

Expression of CDY1 may identify complete spermatogenesisSemantic proximity Read ↗

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