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

Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles.

Nucleic acids research - 11 May 1993

Desmarais E, Vigneron S, Buresi C, Cambien F, Cambou J P, Roizes G

Abstract excerpt

Because of its variations in length, the AT rich Hyper-Variable Region (HVR) of the 3' end of the Apolipoprotein B gene is used as a polymorphic maker in genetic studies. It contains a SspI site in its repeated motif and we used this feature to precisely analyse the internal structure of the different alleles found at this locus in a Caucasian population. We performed total digestion on 194 alleles as well as...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Base Sequence

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosome Mapping

Share to Gene Frequency

Share to Genetic Variation

Share to Molecular Sequence Data

Share to Nucleic Acid Conformation

Share to Restriction Mapping

Source

Open in PubMed Open full text

Identifiers

PMID: 8502559
DOI: 10.1093/nar/21.9.2179
PMCID: PMC309482

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles.PMID 8502559Read ↗

Structural analysis of the minisatellite present at the 3' end of the human apolipoprotein B gene: new definition of the alleles and evolutionary implications.Semantic proximity Read ↗

Allele frequency distribution of the (TG)n(AG)m microsatellite in the apolipoprotein C-II gene.Semantic proximity Read ↗

Hypervariability in a minisatellite 3' of the apolipoprotein B gene: allelic distribution and influence on lipid profiles in Han Children from central China.Semantic proximity Read ↗

Minisatellite variant repeat mapping: application to DNA typing and mutation analysis.Semantic proximity Read ↗

Inferring microevolutionary patterns from allele-size frequency distributions of minisatellite loci: a worldwide study of the APOB 3' hypervariable region polymorphism.Semantic proximity Read ↗

Nucleotide sequence analysis of the apolipoprotein B 3' VNTR.Semantic proximity Read ↗

Internal sequence variations in the Ha-ras variable number tandem repeat rare and common alleles identified by minisatellite variant repeat polymerase chain reaction.Semantic proximity Read ↗

Structure and function of alleles in the 3' end region of human apoB gene.Semantic proximity Read ↗

Length variability and interspersion patterns of the HRAS1 minisatellite: a new approach for the reconstruction of human population relationships.Semantic proximity Read ↗

DNA length polymorphism of the apo B 3' region: frequency distribution of the alleles in the German population.Semantic proximity Read ↗

Highly repeated sites in the apolipoprotein(a) gene recognized by methylated DNA-binding protein, a sequence-specific DNA-binding protein.Semantic proximity Read ↗

Genetic variation at the apoB 3'hypervariable region in a Serbian population.Semantic proximity Read ↗

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