Antithrombin and its inherited deficiencies
- 1 March 1994
- journal article
- research article
- Published by Elsevier in Blood Reviews
- Vol. 8 (1) , 37-55
- https://doi.org/10.1016/0268-960x(94)90006-x
Abstract
No abstract availableKeywords
This publication has 152 references indexed in Scilit:
- Crystal Structure of Cleaved Bovine Antithrombin III at 3·2 Å ResolutionJournal of Molecular Biology, 1993
- Trinucleotide repeat polymorphism in the human antithrombin III (AT3) geneHuman Molecular Genetics, 1993
- Novel point mutations leading to type 1 antithrombin deficiency and thrombosisBritish Journal of Haematology, 1991
- An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA SequencesNew England Journal of Medicine, 1987
- Antithrombin III alger: A new case of Arg 47 ← cys mutationAmerican Journal of Hematology, 1987
- Treatment of Antithrombin III Deficiency with DanazolNew England Journal of Medicine, 1984
- Structure-activity relationship in heparin: A synthetic pentasaccharide with high affinity for antithrombin III and eliciting high anti-factor Xa activityBiochemical and Biophysical Research Communications, 1983
- Mutation of Antitrypsin to AntithrombinNew England Journal of Medicine, 1983
- Molecular Heterogeneity of Inherited Antithrombin III DeficiencyNew England Journal of Medicine, 1983
- A surprising new protein superfamily containing ovalbumin, antithrombin-III, and alpha1-proteinase inhibitorBiochemical and Biophysical Research Communications, 1980