A naturally occurring point mutation in the β3 integrin MIDAS-like domain affects differently αVβ3 and αIIbβ3 receptor function

Thrombosis and Haemostasis

Volumn 86, Issue 6, 2001, Pages 1425-1434

  Morel Kopp, M C ^a   Melchior, C ^a   Chen, P ^a   Ammerlaan, W ^a   Lecompte, T ^a   Kaplan, C ^a   Kieffer, N ^a  

^a UNIVERSITY OF LUXEMBOURG   (Luxembourg)

Author keywords

Cell adhesion; Fibrinogen receptor; Glanzmann thrombasthenia; 3 integrins

Indexed keywords

ARGININE; ASPARTIC ACID; BETA3 INTEGRIN; DITHIOTHREITOL; FIBRIN; FIBRINOGEN RECEPTOR; GLYCINE; INTEGRIN RECEPTOR; LEUCINE; LIGAND; METAL ION; MONOCLONAL ANTIBODY; MONOCLONAL ANTIBODY PAC 1; UNCLASSIFIED DRUG; VITRONECTIN RECEPTOR;

ADHERENT CELL; ARTICLE; CASE REPORT; CELL INTERACTION; CELL MATURATION; CELL SPREADING; CELL SURFACE; CHO CELL; CONFORMATIONAL TRANSITION; EPITOPE MAPPING; FEMALE; FIBRIN CLOT; GENE TRANSLOCATION; GLANZMANN DISEASE; HUMAN; HUMAN CELL; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN MOTIF; PROTEIN PHOSPHORYLATION; PROTEIN SYNTHESIS; PROTEIN SYNTHESIS INHIBITION; PROTEIN TRANSPORT; RIBOSOME SUBUNIT; SIGNAL TRANSDUCTION;

EID: 0035657707     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1616746     Document Type: Article

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