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Thrombosis and Haemostasis|May 4, 1992
Insertions/deletions in the antithrombin gene: 3 mutations associated with non-expressionM Daly, D J Perry, P L Harper, et al.FEBS Letters|August 28, 1989
Antithrombin Cambridge, 384 Ala to Pro: a new variant identified using the polymerase chain reactionD J Perry, P L Harper, S Fairham, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 1, 1996
Type I antithrombin deficiency: five novel mutations associated with thrombosisM Daly, D J Perry, D B Bruce, et al.FEBS Letters|October 29, 1990
Antithrombin Dublin (-3 Val----Glu): an N-terminal variant which has an aberrant signal peptidase cleavage siteM Daly, D Bruce, D J Perry, et al.FEBS Letters|July 22, 1991
Antithrombin Cambridge II, 384 Ala to Ser. Further evidence of the role of the reactive centre loop in the inhibitory function of the serpinsD J Perry, M Daly, P L Harper, et al.British Journal of Haematology|March 1, 1991
The incidence of dysfunctional antithrombin variants: four cases in 210 patients with thromboembolic diseaseP L Harper, R J Luddington, M Daly, et al.Journal of Clinical Pathology|June 1, 1991
Screening for heparin binding variants of antithrombinP L Harper, M Daly, J Price, et al.Molecular Biology & Medicine|June 1, 1989
CpG dinucleotides are "hotspots" for mutation in the antithrombin III gene. Twelve variants identified using the polymerase chain reactionD J Perry, R W CarrellHuman Mutation|January 1, 1996
Molecular genetics of human antithrombin deficiencyD J Perry, R W CarrellJournal of Clinical Pathology|February 1, 1992
Hydrolink gels: a rapid and simple approach to the detection of DNA mutations in thromboembolic diseaseD J Perry, R W CarrellPageof 148