Early attempts to define the character of fibrinogen fragments in serum used
immunoelectrophoretic techniques (Fisher et af, 1967), and these established the similarity …

The fibrinogen and fibrin degradation products (FDP) in serum samples taken from nine
patients with suspected disseminated intravascular coagulation have been characterized …

An extract of human leukocytes was prepared which had marked fibrinogenolytic activity, as
determined by its effect upon the thrombin clotting time of plasminogen-free fibrinogen …

Elution pattern following agarose gel filtration of a fibrinogen solution before and after
freezing. position, determined in separate experiments, of the plasmin resistant fragments D …

An alternative fibrinolytic system, active at physiological pH, is present in peripheral blood
leukocytes. The fibrinolytic proteases localized predominantly in the leukocyte granules are …

Fibrinogen degradation, fibrin polymerisation, and the insertion of cross links into fibrin by
fibrin stabilising factor lead to the appearance of new antigenic determinants. Antibodies …

Three forms of the normal human plasma fibrinogen γ-chain which differ in molecular weight
have been purified. Plasma fibrinogen was separated by ion exchange chromatography on …

Purified fibrinogen was lysed by plasmin and the degradation products identified by gel
filtration, immunoelectrophoresis and the tanned red cell haem‐agglutination inhibition …

The behaviour of labelled des‐AB fibrin in plasma was studied by gel filtration after it had
been injected into rabbits. Purified rabbit [125I] des‐AB fibrin was prepared by clotting of …

Two types of normal human plasma fibrinogen--peak 1 and peak 2--are distinquishable by
DEAE-cellulose gradient elution chromatography. The elution characteristics of peak 2 …