The genetic association of the FPRL1 promoter polymorphism with chronic urticaria in a Korean population

Ann Allergy Asthma Immunol. 2010 Jul;105(1):96-7. doi: 10.1016/j.anai.2010.05.003.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell Migration Assays
  • Cells, Cultured
  • Chemotaxis / drug effects
  • Chemotaxis / genetics
  • Chronic Disease
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Humans
  • Immunoglobulin E / blood
  • Korea
  • Male
  • Neutrophils / drug effects
  • Neutrophils / immunology
  • Neutrophils / metabolism*
  • Neutrophils / pathology
  • Polymorphism, Single Nucleotide
  • Promoter Regions, Genetic
  • Receptors, Formyl Peptide / genetics*
  • Receptors, Formyl Peptide / metabolism
  • Receptors, Lipoxin / genetics*
  • Receptors, Lipoxin / metabolism
  • Urticaria / genetics*
  • Urticaria / immunology
  • Urticaria / metabolism

Substances

  • FPR2 protein, human
  • Receptors, Formyl Peptide
  • Receptors, Lipoxin
  • Immunoglobulin E