Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Unknown (R22)
Project #
5R22AI024349-02
Application #
3444957
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1986-12-01
Project End
1989-11-30
Budget Start
1987-12-01
Budget End
1988-11-30
Support Year
2
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Barnes, D A; Wollish, W; Nelson, R G et al. (1995) Plasmodium falciparum: D260, an intraerythrocytic parasite protein, is a member of the glutamic acid dipeptide-repeat family of proteins. Exp Parasitol 81:79-89
Petersen, C; Nelson, R; Leech, J et al. (1990) The gene product of the Plasmodium falciparum 11.1 locus is a protein larger than one megadalton. Mol Biochem Parasitol 42:189-95
Rosenthal, P J; McKerrow, J H; Rasnick, D et al. (1989) Plasmodium falciparum: inhibitors of lysosomal cysteine proteinases inhibit a trophozoite proteinase and block parasite development. Mol Biochem Parasitol 35:177-83
Petersen, C; Nelson, R; Magowan, C et al. (1989) The mature erythrocyte surface antigen of Plasmodium falciparum is not required for knobs or cytoadherence. Mol Biochem Parasitol 36:61-5
Magowan, C; Wollish, W; Anderson, L et al. (1988) Cytoadherence by Plasmodium falciparum-infected erythrocytes is correlated with the expression of a family of variable proteins on infected erythrocytes. J Exp Med 168:1307-20
Rosenthal, P J; McKerrow, J H; Aikawa, M et al. (1988) A malarial cysteine proteinase is necessary for hemoglobin degradation by Plasmodium falciparum. J Clin Invest 82:1560-6
Rosenthal, P J; Kim, K; McKerrow, J H et al. (1987) Identification of three stage-specific proteinases of Plasmodium falciparum. J Exp Med 166:816-21