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

Kell, Kx and the McLeod syndrome.

Bailliere's best practice & research. Clinical haematology - 1 Dec 1999

Redman C M, Russo D, Lee S

Abstract excerpt

The antigens of the Kell blood group system are carried on a 93 kDa type II glycoprotein encoded by a single gene on chromosome 7 at 7q33. XK is a 50.9 kDa protein that traverses the membrane ten times and derives from a single gene on the X chromosome at Xp21. A single disulphide bond, Kell Cys 72-XK Cys 347, links Kell to XK. The Kell component of the Kell/XK complex is important in transfusion medicine since...

Read the complete abstract on PubMed

Topics

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

Share to Hematopoietic System
Share to Kell Blood-Group System
Share to Neuromuscular Diseases

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

Share to Syndrome

Share to X Chromosome

Share to Amino Acid Transport Systems, Neutral

Share to Carrier Proteins

Share to Genetic Linkage

Source

Identifiers

PMID: 10895256
DOI: 10.1053/beha.1999.0045

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

Kell, Kx and the McLeod syndrome.PMID 10895256Read ↗

The Kell blood group system: Kell and XK membrane proteins.Semantic proximity Read ↗

Functional and structural aspects of the Kell blood group system.Semantic proximity Read ↗

Kell and Kx blood group systems.Semantic proximity Read ↗

Association of XK and Kell Blood Group ProteinsSemantic proximity Read ↗

A McLeod phenotype detected by random screening for K:-4 [Kp(b-)] blood donors in Brazil.Semantic proximity Read ↗

McLeod syndrome: a neurohaematological disorderSemantic proximity Read ↗

A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cells.Semantic proximity Read ↗

Molecular Basis and Clinical Overview of McLeod Syndrome Compared With Other Neuroacanthocytosis SyndromesSemantic proximity Read ↗

How we approach transfusions in a patient with high risk of alloimmunization from McLeod phenotype.Semantic proximity Read ↗

McLeod phenotype without the McLeod syndrome.Semantic proximity Read ↗

Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases.Semantic proximity Read ↗

The Kell blood group system and the McLeod phenotype.Semantic proximity Read ↗

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