Inherited platelet-based bleeding disorders
- 1 July 2003
- journal article
- review article
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 1 (7) , 1628-1636
- https://doi.org/10.1046/j.1538-7836.2003.00266.x
Abstract
No abstract availableKeywords
This publication has 87 references indexed in Scilit:
- ADP Is the Cognate Ligand for the Orphan G Protein-coupled Receptor SP1999Journal of Biological Chemistry, 2001
- Binding of Thrombin to Glycoprotein Ib Accelerates the Hydrolysis of Par-1 on Intact PlateletsJournal of Biological Chemistry, 2001
- ADP can induce aggregation of human platelets via both P2Y1 and P2T receptorsBritish Journal of Pharmacology, 2000
- Clinical, Molecular, and Cell Biological Aspects of Chediak–Higashi SyndromeMolecular Genetics and Metabolism, 1999
- Role of the Extracellular Loops of G Protein-Coupled Receptors in Ligand Recognition: A Molecular Modeling Study of the Human P2Y1ReceptorBiochemistry, 1999
- A Novel Association of Fc Receptor γ-Chain with Glycoprotein VI and Their Co-expression as a Collagen Receptor in Human PlateletsJournal of Biological Chemistry, 1997
- An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets. Its influence on glycoprotein IIb-IIIa complex function.Journal of Clinical Investigation, 1995
- Arg60 to Leu mutation of the human thromboxane A2 receptor in a dominantly inherited bleeding disorder.Journal of Clinical Investigation, 1994
- ATP‐ADP compartmentation in storage pool deficient platelets: correlation between granule‐bound ADP and the bleeding timeBritish Journal of Haematology, 1983
- Constitutional Thrombocytopathy with Subnormal Response to Thromboxane A2British Journal of Haematology, 1981