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

Three novel allelic variants of the RAET1E/ULBP4 gene in humans.

Tissue antigens - 1 Oct 2012

Cox S T, Madrigal J A, Saudemont A

Abstract excerpt

Discovery of three novel alleles of RAET1E/ULBP4 by sequence-based typing: RAET1E*008, RAET1E*009 and RAET1E*010.

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 6
Share to Ethnicity
Share to Histocompatibility Antigens Class I
Share to Killer Cells, Natural

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ligands

Share to Molecular Typing

Share to NK Cell Lectin-Like Receptor Subfamily K

Share to Protein Isoforms

Source

Identifiers

PMID: 22845659
DOI: 10.1111/j.1399-0039.2012.01933.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Three novel allelic variants of the RAET1E/ULBP4 gene in humans.PMID 22845659Read ↗

Further polymorphism of the RAET1E/ULBP4 gene in humans.Semantic proximity Read ↗

Increasing polymorphism of the RAET1E/ULBP4 gene in humans.Semantic proximity Read ↗

Characterisation of RAET1E/ULBP4 exon 4 and 3' untranslated region genetic architecture reveals further diversity and allelic polymorphism.Semantic proximity Read ↗

Polymorphisms of NKG2D ligands: diverse RAET1/ULBP genes in northeastern Thais.Semantic proximity Read ↗

The nuclear receptor subfamily 4 group A1 in human diseaseSemantic proximity Read ↗

A highly informative dinucleotide repeat polymorphism at D13S201, between RB1 and WND.Semantic proximity Read ↗

Clinical phenotype and mutant TRα1.Semantic proximity Read ↗

Single nucleotide polymorphism analysis of the NKG2D ligand cluster on the long arm of chromosome 6: Extensive polymorphisms and evidence of diversity between human populations.Semantic proximity Read ↗

RAET1/ULBP alleles and haplotypes among Kolla South American Indians.Semantic proximity Read ↗

ACTN1 variants associated with thrombocytopenia.Semantic proximity Read ↗

Cellular Expression, Trafficking, and Function of Two Isoforms of Human ULBP5/RAET1GSemantic proximity Read ↗

E4BP4 overexpression: A protective mechanism in CD4+ T cells from SLE patientsSemantic proximity Read ↗

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