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

An HLB-B null allele (B*0808N) caused by a nucleotide deletion in exon 3, found in the family of a bone marrow transplant recipient.

Tissue antigens - 1 Jan 2000

Carter V, Dunn P P, Cavanagh G, Day S, Ross J, Chapman C

Abstract excerpt

We have identified a variant HLA-B allele, B*0808N, segregating through two generations of healthy individuals, whilst HLA typing the family of a bone marrow patient. Serological typing identified a disparity between the father (A1, A3 B7 DR7) and the brother (A1, A2 B56 DR1, DR7) of the patient. Low/medium resolution polymerase chain reaction using sequence-specific primers (PCR-SSP) revealed a B*08 allele...

Read the complete abstract on PubMed

Topics

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

Share to Bone Marrow Transplantation
Share to Codon, Terminator

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

Share to DNA Primers

Share to Frameshift Mutation

Share to HLA-B8 Antigen

Share to Polymerase Chain Reaction

Share to Sequence Deletion

Source

Identifiers

PMID: 10703611
DOI: 10.1034/j.1399-0039.2000.550111.x

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

An HLB-B null allele (B*0808N) caused by a nucleotide deletion in exon 3, found in the family of a bone marrow transplant recipient.PMID 10703611Read ↗

HLA-B*0749N: the first HLA-B*07 null allele.Semantic proximity Read ↗

The Novel HLA-C*07:01:130 Allele, Identified by Next-Generation Sequencing in a Greek Haematopoietic Stem Cell Donor.Semantic proximity Read ↗

A new non-expressed allele HLA-A*03:168N, identified by serological and sequence-based typing in a voluntary Norwegian hematopoietic stem cell donor.Semantic proximity Read ↗

Characterization of the novel HLA-C*07:195 allele in an Italian hematopoietic stem cell volunteer donor, detected by sequence-based typing.Semantic proximity Read ↗

The Full-Length Genomic Sequence of the HLA-A*02:07:08 Allele.Semantic proximity Read ↗

Identification of a new HLA-A null allele, A*30:59N, with a stop codon in exon 3, by sequence-based typing.Semantic proximity Read ↗

Sequencing of four new HLA-C alleles, Cw*070403, Cw*0757, Cw*1705, and Cw*0223.Semantic proximity Read ↗

A novel HLA-Cw*07 variant, HLA-Cw*0760, identified by sequence-based typing in a bone marrow donor.Semantic proximity Read ↗

Description of HLA-A*0127N, a novel nonexpressed allele identified by SBT.Semantic proximity Read ↗

Identification of a new HLA-B*08 variant, HLA-B*0804.Semantic proximity Read ↗

Three New Null HLA Alleles Were Identified of the Unrelated Bone Marrow Donors.Semantic proximity Read ↗

A single nucleotide deletion in exon 3 of the HLA-C*07:02:01:01 allele produces a novel HLA-C*07 null allele, HLA-C*07:393N.Semantic proximity Read ↗

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