Associated Papers
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
Role of genetic factors in the pathogenesis of aggressive periodontitis.
Vieira AR et al.
Periodontology 2000, 2014
V101L of human formyl peptide receptor 1 (FPR1) increases receptor affinity and augments the antagonism mediated by cyclosporins.
Zhou C et al.
The Biochemical Journal, 2013
Assessment of computational methods for predicting the effects of missense mutations in human cancers.
Gnad F et al.
Bmc Genomics, 2013
23819521 (PubMed )
Supplement: 1471-2164-14-S3-S7-S1.xlsx › COSMIC
Functional polymorphisms of the FPR1 gene and aggressive periodontitis in Japanese.
Gunji T et al.
Biochemical and Biophysical Research Communications, 2007
Impact of GPCRs in clinical medicine: monogenic diseases, genetic variants and drug targets.
Insel PA et al.
Biochimica Et Biophysica Acta, 2007
The role of genetic polymorphisms in periodontitis.
Yoshie H et al.
Periodontology 2000, 2007
Mutations of F110 and C126 of the formyl peptide receptor interfere with G-protein coupling and chemotaxis.
Jones BE et al.
Journal of Periodontology, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients.
Zhang Y et al.
Genes and Immunity, 2003
Contrasting evolution of the human leukocyte N-formylpeptide receptor subtypes FPR and FPRL1R.
Sahagun-Ruiz A et al.
Genes and Immunity, 2001
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