Extensive genetic polymorphism in the human tumor necrosis factor region and relation to extended HLA haplotypes

190Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.
Get full text

Abstract

We have identified three polymorphic microsatellites (which we call TNFa, TNFb, and TNFc) within a 12-kilobase region of the human major histocompatibility complex (MHC) that includes the tumor necrosis factor (TNF) locus. TNFc is located within the first intron of the TNF-β gene and has only 2 alleles. TNFa and TNFb are 3.5 kilobases upstream (telomeric) of the TNF-β gene and have at least 13 and 7 alleles, respectively. TNFa, -b, and -c alleles are in linkage disequilibrium with alleles at other loci within the MHC, including class I, class II, and class III. TNFa, -b, and -c alleles are also associated with extended HLA haplotypes. These TNF polymorphisms will allow a thorough genetic analysis of the involvement of TNF in MHC-linked pathologies.

Cite

CITATION STYLE

APA

Jongeneel, C. V., Briant, L., Udalova, I. A., Sevin, A., Nedospasov, S. A., & Cambon-Thomsen, A. (1991). Extensive genetic polymorphism in the human tumor necrosis factor region and relation to extended HLA haplotypes. Proceedings of the National Academy of Sciences of the United States of America, 88(21), 9717–9721. https://doi.org/10.1073/pnas.88.21.9717

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free