Associated Papers
Whole-exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer's disease.
Patel T et al.
Neuropathology and Applied Neurobiology, 2018
Formyl Peptide Receptor Polymorphisms: 27 Most Possible Ways for Phagocyte Dysfunction.
Skvortsov SS et al.
Biochemistry. Biokhimiia, 2017
FPR1 interacts with CFH, HTRA1 and smoking in exudative age-related macular degeneration and polypoidal choroidal vasculopathy.
Liang XY et al.
Eye (london, England), 2014
Human formyl peptide receptor 1 (FPR1) c.32C>T SNP is associated with decreased soluble E-selectin levels.
Benachour H et al.
Pharmacogenomics, 2009
Analysis of a missense variant of the human N-formyl peptide receptor that is associated with agonist-independent beta-arrestin association and indices of inflammation.
Bhattacharya M et al.
The Pharmacogenomics Journal, 2007
Contrasting evolution of the human leukocyte N-formylpeptide receptor subtypes FPR and FPRL1R.
Sahagun-Ruiz A et al.
Genes and Immunity, 2001
Select a paper to view details