A 3'UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility. [electronic resource]
- Biochimica et biophysica acta 10 2016
- 1306-13 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0006-3002
10.1016/j.bbagrm.2016.07.006 doi
3' Untranslated Regions Alleles Antigens, CD1d--genetics B-Cell Activating Factor--genetics Base Sequence Binding Sites CTLA-4 Antigen--genetics Case-Control Studies DNA Mutational Analysis Gene Expression Regulation Gene Frequency Genetic Predisposition to Disease Haplotypes Humans Lectins, C-Type--genetics Membrane Proteins--genetics MicroRNAs--genetics Mutation NK Cell Lectin-Like Receptor Subfamily D--genetics Pemphigus--diagnosis Polymorphism, Single Nucleotide Receptors, Immunologic Trans-Activators--genetics