Analysis of CD36 Binding Domains: Ligand Specificity Controlled by Dephosphorylation of an Ectodomain
Author:
Affiliation:
1. Division of Hematology-Oncology, Cornell University Medical College, New York, NY 10021.
2. Department of Molecular Parasitology, New York University Medical School, New York, NY 10010.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference31 articles.
1. ASCH A unpublished data.
2. ASCH, A.S., THROMBOSPONDIN SEQUENCE MOTIF (CSVTCG) IS RESPONSIBLE FOR CD36-BINDING, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 182: 1208 (1992).
3. ASCH, A.S., ISOLATION OF THE THROMBOSPONDIN MEMBRANE-RECEPTOR, JOURNAL OF CLINICAL INVESTIGATION 79: 1054 (1987).
4. BARNWELL, J.W., A HUMAN 88-KD MEMBRANE GLYCOPROTEIN (CD36) FUNCTIONS INVITRO AS A RECEPTOR FOR A CYTOADHERENCE LIGAND ON PLASMODIUM-FALCIPARUM-INFECTED ERYTHROCYTES, JOURNAL OF CLINICAL INVESTIGATION 84: 765 (1989).
5. BARNWELL, J.W., MONOCLONAL-ANTIBODY OKM5 INHIBITS THE INVITRO BINDING OF PLASMODIUM-FALCIPARUM-INFECTED ERYTHROCYTES TO MONOCYTES, ENDOTHELIAL, AND C32 MELANOMA-CELLS, JOURNAL OF IMMUNOLOGY 135: 3494 (1985).
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