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

Functional polymorphism in H2BFWT‐5′UTR is associated with susceptibility to male infertility

6 Jul 2009

Abstract excerpt

H2B histone family, member W, testis-specific (H2BFWT) gene encodes a testis-specific histone that becomes incorporated into sperm chromatin. A male infertility-associated single nucleotide polymorphism (-9C > T) within the 5' untranslated region (5'UTR) of the H2BFWT gene was identified by direct sequencing. Statistical association studies showed the polymorphism significantly associated with male infertility (n...

Read the complete abstract on PubMed

Topics

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

Share to Epigenetics and DNA Methylation
Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19583817
DOI: 10.1111/j.1582-4934.2009.00830.x

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

Functional polymorphism in H2BFWT‐5′UTR is associated with susceptibility to male infertilityPMID 19583817Read ↗

Association between two common transitions of H2BFWT gene and male infertility: a case-control, meta, and structural analysis.Semantic proximity Read ↗

Association of the c.-9C>T and c.368A>G transitions in H2BFWT gene with male infertility in an Iranian population.Semantic proximity Read ↗

Relationship of SNP of H2BFWT gene to male infertility in a Chinese population with idiopathic spermatogenesis impairment.Semantic proximity Read ↗

[Association of single nucleotide polymorphisms in H2BFWT with male infertility in southwest China].Semantic proximity Read ↗

H2BFWT Variations in Sperm DNA and Its Correlation to PregnancySemantic proximity Read ↗

H2BFWT Variations in Sperm DNA and Its Correlation to Pregnancy.Semantic proximity Read ↗

Testis-specific H2B.W1 disrupts nucleosome integrity by reducing DNA-histone interactions.Semantic proximity Read ↗

Single nucleotide polymorphism at 5' UTR of H2BC1 and promoter methylation influence TSH2B expression.Semantic proximity Read ↗

Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure.Semantic proximity Read ↗

Human testis/sperm-specific histone H2B (hTSH2B). Molecular cloning and characterization.Semantic proximity Read ↗

Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility.Semantic proximity Read ↗

Family-Based Study Reveals PDE11A/PDE11A-AS1 Variants in Testicular Germ Cell Tumor Predisposition.Semantic proximity Read ↗

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