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

Characterization of DDX4 Gene Expression in Human Cases with Non-Obstructive Azoospermia and in Sterile and Fertile Mice

17 Mar 2021

Abstract excerpt

BACKGROUND: In mammals, spermatogenesis is the main process for male fertility that is initiated by spermatogonial stem cells (SSCs) proliferation. SSCs are unipotent progenitor cells accountable for transferring the genetic information to the following generation by differentiating to haploid cells during spermato-and spermiogenesis. DEAD-box helicase 4 (DDX4) is a specific germ cell marker and its expression...

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 Sperm and Testicular Function
Share to Testicular diseases and treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34041004
DOI: 10.18502/jri.v22i2.5793

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of DDX4 Gene Expression in Human Cases with Non-Obstructive Azoospermia and in Sterile and Fertile MicePMID 34041004Read ↗

RNA helicase DDX5 acts as a critical regulator for survival of neonatal mouse gonocytes.Semantic proximity Read ↗

Sertoli and Germ Cells Within Atrophic Seminiferous Tubules of Men With Non-Obstructive AzoospermiaSemantic proximity Read ↗

DDX5 plays essential transcriptional and post-transcriptional roles in the maintenance and function of spermatogoniaSemantic proximity Read ↗

Epigenetics of nonobstructive azoospermiaSemantic proximity Read ↗

Human X chromosome exome sequencing identifies BCORL1 as contributor to spermatogenesisSemantic proximity Read ↗

Sequencing of a ‘mouse azoospermia’ gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrestSemantic proximity Read ↗

Transcriptome Analysis to Identify Human Spermatogonial Cells from Sertoli Cell-Only TestesSemantic proximity Read ↗

Transcriptomic analysis of the Non-Obstructive Azoospermia (NOA) to address gene expression regulation in human testisSemantic proximity Read ↗

Discrimination and characterization of Sertoli cell-only syndrome in non-obstructive azoospermia using cell-free seminal DDX4.Semantic proximity Read ↗

ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia.Semantic proximity Read ↗

Mechanism and potential therapeutic strategies of genetic abnormalities involved in deoxyribonucleic acid double-strand breaks leading to the development of human non-obstructive azoospermia.Semantic proximity Read ↗

Adult human and mouse ovaries lack DDX4-expressing functional oogonial stem cellsSemantic proximity Read ↗

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