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

Association between the apolipoprotein B signal peptide gene insertion/deletion polymorphism and male infertility.

Molecular human reproduction - 1 Dec 2006

Peterlin B, Zorn B, Volk M, Kunej T

Abstract excerpt

In male mice heterozygous for a null apolipoprotein B (apoB), allele infertility was noticed. These data led us to investigate a possible role of APOB gene polymorphism and male infertility in humans. In this case-control study, we searched for an association between the insertion/deletion (I/D) polymorphism of the APOB gene and male infertility in 560 Slovene Caucasian men. The study group consisted of 310...

Read the complete abstract on PubMed

Topics

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

Share to Asthenozoospermia
Share to Azoospermia
Share to Follicle Stimulating Hormone

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Oligospermia

Share to Protein Sorting Signals

Share to Sertoli Cells

Share to Slovenia

Share to Sperm Motility

Source

Identifiers

PMID: 17071710
DOI: 10.1093/molehr/gal088

Genes

OAT
APOB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Association between the apolipoprotein B signal peptide gene insertion/deletion polymorphism and male infertility.PMID 17071710Read ↗

APOB gene signal peptide deletion polymorphism is not associated with infertility in Indian men.Semantic proximity Read ↗

Association study of single-nucleotide polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 genes with male infertility.Semantic proximity Read ↗

Involvement of CFTR gene alterations in obstructive and nonobstructive infertility in men.Semantic proximity Read ↗

Association between male infertility and androgen receptor mutations in Brazilian patients.Semantic proximity Read ↗

Human INHBB Gene Variant (c.1079T>C:p.Met360Thr) Alters Testis Germ Cell Content, but Does Not Impact Fertility in Mice.Semantic proximity Read ↗

Association of molecular variants of luteinizing hormone with male infertilitySemantic proximity Read ↗

KIR and HLA-C genes in male infertility.Semantic proximity Read ↗

Mutant phenotype analysis suggests potential roles for C-type natriuretic peptide receptor (NPR-B) in male mouse fertility.Semantic proximity Read ↗

Genetic polymorphisms of hspa1b and hspa1l in infertile men.Semantic proximity Read ↗

The effect of a partial Y chromosome deletion in B10.BR-Y <i>del</i> mice on testis morphology, sperm quality and efficiency of fertilizationSemantic proximity Read ↗

Inhibin B as a Serum Marker of Spermatogenesis: Correlation to Differences in Sperm Concentration and Follicle-Stimulating Hormone Levels. A Study of 349 Danish Men<sup>1</sup>Semantic proximity Read ↗

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