Decay accelerating activity of complement receptor type 1 (CD35). Two active sites are required for dissociating C5 convertases.

Autor: Krych-Goldberg, M, Hauhart, R E, Subramanian, V B, Yurcisin, B M, Crimmins, D L, Hourcade, D E, Atkinson, J P

Publikováno v: Journal of Biological Chemistry; October 1999, Vol. 274 Issue: 44 p31160-8, 9p

A conserved element in the serine protease domain of complement factor B.

Autor: Hourcade, D E, Mitchell, L M, Oglesby, T J

Publikováno v: Journal of Biological Chemistry; October 1998, Vol. 273 Issue: 40 p25996-6000, 5p

Expansion of the Knops blood group system and subdivision of Sl(a).

Autor: Moulds JM; Department of Microbiology and Immunology, MCP Hahnemann University School of Medicine, Philadelphia, Pennsylvania 19129, USA. moulds@drexel.edu, Zimmerman PA, Doumbo OK, Diallo DA, Atkinson JP, Krych-Goldberg M, Hourcade DE, Moulds JJ

Publikováno v: Transfusion [Transfusion] 2002 Feb; Vol. 42 (2), pp. 251-6.

Molecular identification of Knops blood group polymorphisms found in long homologous region D of complement receptor 1.

Autor: Moulds JM; University of Texas-Houston Medical School, USA. moulds@drexel.edu, Zimmerman PA, Doumbo OK, Kassambara L, Sagara I, Diallo DA, Atkinson JP, Krych-Goldberg M, Hauhart RE, Hourcade DE, McNamara DT, Birmingham DJ, Rowe JA, Moulds JJ, Miller LH

Publikováno v: Blood [Blood] 2001 May 01; Vol. 97 (9), pp. 2879-85.

Mutations of the type A domain of complement factor B that promote high-affinity C3b-binding.

Autor: Hourcade DE; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA. dhourcad@im.wustl.edu, Mitchell LM, Oglesby TJ

Publikováno v: Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 1999 Mar 01; Vol. 162 (5), pp. 2906-11.