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Volumn 16, Issue 2, 1996, Pages 114-138
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Molecular basis and clinical aspects of hereditary megakaryocyte and platelet membrane glycoprotein disorders
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Author keywords
Bernard Soulier syndrome; Glanzmann's thrombasthenia; Membrane glycoprotein receptors; Platelet type von Willebrand's disease
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Indexed keywords
ADENOSINE DIPHOSPHATE;
ADRENALIN;
AMINO ACID;
CALCIUM;
CALMODULIN;
CD34 ANTIGEN;
CD36 ANTIGEN;
COLLAGEN;
CYSTEINE;
FIBRINOGEN;
FIBRINOGEN RECEPTOR;
FIBRONECTIN;
GLYCOPROTEIN;
GLYCOPROTEIN IB;
GLYCOPROTEIN IIB;
GLYCOPROTEIN IIIA;
GLYCOPROTEIN IX;
GLYCOPROTEIN V;
INTEGRIN;
LAMININ;
RECEPTOR;
RISTOCETIN;
THROMBIN;
THROMBOCYTE ANTIGEN;
THROMBOSPONDIN;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
VERY LATE ACTIVATION ANTIGEN;
VERY LATE ACTIVATION ANTIGEN 2;
VITRONECTIN;
VON WILLEBRAND FACTOR;
BERNARD SOULIER DISEASE;
BINDING SITE;
BIOSYNTHESIS;
BLEEDING;
BURST FORMING UNIT;
COLONY FORMING UNIT;
DISEASE CLASSIFICATION;
ENZYME LINKED IMMUNOSORBENT ASSAY;
GLANZMANN DISEASE;
HUMAN;
IMMUNOCHEMISTRY;
IMMUNOPHENOTYPING;
IMMUNORADIOMETRIC ASSAY;
MEGAKARYOCYTE;
NONHUMAN;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
PROTEIN EXPRESSION;
REVIEW;
STRUCTURE ACTIVITY RELATION;
THROMBOCYTE;
THROMBOCYTE ADHESION;
THROMBOCYTE AGGREGATION;
THROMBOCYTE MEMBRANE;
VON WILLEBRAND DISEASE;
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EID: 0030054845
PISSN: 07209355
EISSN: None
Source Type: Journal
DOI: 10.1055/s-0038-1656647 Document Type: Review |
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Times cited : (14)
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References (0)
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