CareLit Fachartikel

Molecular Basis and Clinical Aspects of Hereditary Megakaryocyte and Platelet Membrane Glycoprotein Disorders

Scharf, R.-E. · Zeitschrift für Orthopädie und Unfallchirurgie · 1996 · Heft 02 · S. 114 bis 138

Dokument
615094
CareLit-ID
Jahr
1996
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Zeitschrift für Orthopädie und Unfallchirurgie
Autor:innen
Scharf, R.-E.
Ausgabe
Heft 02 / 1996
Jahrgang 16
Seiten
114 bis 138
Erschienen: 1996-04-01 00:00:00
ISSN
0720-9355;2567-5761

Zusammenfassung

SummarySpecific membrane glycoproteins (GP) expressed by the megakaryocyte-platelet system, including GPIa-lla, GPIb-V-IX, GPIIb-llla, and GPIV are involved in mediat-ing platelet adhesion to the subendothelial matrix. Among these glycoproteins, GPIIb-llla plays a pivotal role since platelet aggregation is exclusively mediated by this receptor and its interaction with soluble macromolecular proteins. Inherited defects of the GPIIb-llla or GPIb-V-IX receptor complexes are associated with bleeding disorders, known as Glanzmann's thrombasthenia, Bernard-Soulier syndrome, or platelet-type von Willebrand's disease, r…

Schlagworte

Bernard-Soulier Syndrome Biology Zeitschrift für Orthopädie und Unfallchirurgie