Molecular Variation of Human Fibrinogen
- 1 January 1970
- book chapter
- Published by Elsevier
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Chromatographic, ultracentrifugal, and related studies of fibrinogen “Baltimore”Journal of Clinical Investigation, 1969
- Congenital dysfibrinogenemia: fibrinogen detroitJournal of Clinical Investigation, 1969
- Fibrinogen Detroit—a Molecular Defect in the N-terminal Disulphide Knot of Human Fibrinogen?Nature, 1968
- Structure of N-terminal Fragments of Fibrinogen and Specificity of ThrombinNature, 1967
- Familial Disturbance of Fibrin Monomer AggregationBritish Journal of Haematology, 1966
- A New Inherited Coagulation Disorder Caused by an Abnormal Fibrinogen (‘Fibrinogen Baltimore’)Nature, 1965
- Physicochemical studies of bovine fibrinogen III. Optical rotation of the native and denatured moleculeBiochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis, 1965
- Anomalous behaviour of haemophilia A fibrinogen during ultracentrifugationBiochimica et Biophysica Acta (BBA) - General Subjects, 1965
- Fetales FibrinogenKlinische Wochenschrift, 1963
- PATHOGENESIS OF THE COAGULATION DEFECT DEVELOPING DURING PATHOLOGICAL PLASMA PROTEOLYTIC (“FIBRINOLYTIC”) STATES. I. THE SIGNIFICANCE OF FIBRINOGEN PROTEOLYSIS AND CIRCULATING FIBRINOGEN BREAKDOWN PRODUCTS*Journal of Clinical Investigation, 1962