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Dennis E. Hourcade

Washington University School of Medicine

Department of Medicine

Division of Rheumatology

St. Louis

USA

[email]@im.wustl.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Washington University School of Medicine, Department of Medicine, Division of Rheumatology, St. Louis, USA. 2002 - 2008
  • Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA. 1998 - 2006

References

  1. Properdin and complement activation: a fresh perspective. Hourcade, D.E. Curr. Drug. Targets (2008) [Pubmed]
  2. The role of properdin in the assembly of the alternative pathway C3 convertases of complement. Hourcade, D.E. J. Biol. Chem. (2006) [Pubmed]
  3. Decay-accelerating factor (DAF), complement receptor 1 (CR1), and factor H dissociate the complement AP C3 convertase (C3bBb) via sites on the type A domain of Bb. Hourcade, D.E., Mitchell, L., Kuttner-Kondo, L.A., Atkinson, J.P., Medof, M.E. J. Biol. Chem. (2002) [Pubmed]
  4. Mutations of the type A domain of complement factor B that promote high-affinity C3b-binding. Hourcade, D.E., Mitchell, L.M., Oglesby, T.J. J. Immunol. (1999) [Pubmed]
  5. Decay acceleration of the complement alternative pathway C3 convertase. Hourcade, D.E., Mitchell, L.M., Medof, M.E. Immunopharmacology (1999) [Pubmed]
  6. A conserved element in the serine protease domain of complement factor B. Hourcade, D.E., Mitchell, L.M., Oglesby, T.J. J. Biol. Chem. (1998) [Pubmed]
 
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