Genetic determinants of arterial thrombosis.
BEST PRACT RES CL HA
505 - 532.
This chapter describes examples of genetic variation involved in the function or regulation of a number of haemostatic proteins involved in the thrombotic process. In each case, the data suggest associations between genotype and disease and, particularly in the case of fibrinogen, PAI-I, Factor VII and Factor XIII, there is interaction between genotype and environment in determination of the relevant plasma level, providing a possible explanation for the differential response of individuals to their environment.
|Title:||Genetic determinants of arterial thrombosis|
|Keywords:||polymorphisms, genes, coagulation, fibrinolysis, platelets, myocardial infarction, PLASMINOGEN-ACTIVATOR INHIBITOR-1, BETA-FIBRINOGEN GENE, ISCHEMIC-HEART-DISEASE, COAGULATION-FACTOR-XIII, ACUTE MYOCARDIAL-INFARCTION, PLATELET GLYCOPROTEIN IIIA, ACUTE-PHASE REACTION, FACTOR-VII GENE, A-SUBUNIT GENE, 4G/5G PROMOTER POLYMORPHISM|
|UCL classification:||UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science
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