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FEBS Letters
|
March 25, 1991
P1 variant antithrombins Glasgow (393 Arg to His) and Pescara (393 Arg to Pro) have increased heparin affinity and are resistant to catalytic cleavage by elastase. Implications for the heparin activation mechanism
M C Owen, P M George, D A Lane, et al.
Clinical Nephrology
|
December 1, 1989
A low molecular weight heparin ("fragmin") for routine hemodialysis: a crossover trial comparing three dose regimens with a standard regimen of commercial unfractionated heparin
E Anastassiades, D A Lane, H Ireland, et al.
Blood
|
March 1, 1985
Specific identification of fibrin polymers, fibrinogen degradation products, and crosslinked fibrin degradation products in plasma and serum with a new sensitive technique
D G Connaghan, C W Francis, D A Lane, et al.
British Journal of Haematology
|
September 1, 1996
Prenatal diagnosis in combined antithrombin and factor V gene mutation
D A Lane, K Auberger, H Ireland, et al.
British Journal of Haematology
|
November 1, 1988
Relationship between ex vivo anti-proteinase (factor Xa and thrombin) assays and in vivo anticoagulant effect of very low molecular weight heparin, CY222
C J Tew, D A Lane, E Thompson, et al.
Thrombosis and Haemostasis
|
February 1, 1994
Low affinity heparin is an antithrombotic agent
E Gray, S Cesmeli, J C Lormeau, et al.
Seminars in Thrombosis and Hemostasis
|
January 1, 1994
Antithrombin: the principal inhibitor of thrombin
R J Olds, D A Lane, B Mille, et al.
The Journal of Biological Chemistry
|
November 25, 1994
Role of N- and C-terminal amino acids in antithrombin binding to pentasaccharide
B Mille, J Watton, T W Barrowcliffe, et al.
Acta Chirurgica Scandinavica. Supplementum
|
January 1, 1988
Equivalent effective doses of heparin and low molecular weight heparin(oid)s in haemodialysis for chronic renal failure
D A Lane, H Ireland, C J Tew, et al.
Blood
|
December 1, 1990
A frameshift mutation leading to type 1 antithrombin deficiency and thrombosis
R J Olds, D A Lane, G Finazzi, et al.
Page
of 27
Search research articles
Search
Showing results (141-150 of 265) with videos related to
Sort By:
Page
of 27
FEBS Letters
|
March 25, 1991
P1 variant antithrombins Glasgow (393 Arg to His) and Pescara (393 Arg to Pro) have increased heparin affinity and are resistant to catalytic cleavage by elastase. Implications for the heparin activation mechanism
M C Owen, P M George, D A Lane, et al.
Clinical Nephrology
|
December 1, 1989
A low molecular weight heparin ("fragmin") for routine hemodialysis: a crossover trial comparing three dose regimens with a standard regimen of commercial unfractionated heparin
E Anastassiades, D A Lane, H Ireland, et al.
Blood
|
March 1, 1985
Specific identification of fibrin polymers, fibrinogen degradation products, and crosslinked fibrin degradation products in plasma and serum with a new sensitive technique
D G Connaghan, C W Francis, D A Lane, et al.
British Journal of Haematology
|
September 1, 1996
Prenatal diagnosis in combined antithrombin and factor V gene mutation
D A Lane, K Auberger, H Ireland, et al.
British Journal of Haematology
|
November 1, 1988
Relationship between ex vivo anti-proteinase (factor Xa and thrombin) assays and in vivo anticoagulant effect of very low molecular weight heparin, CY222
C J Tew, D A Lane, E Thompson, et al.
Thrombosis and Haemostasis
|
February 1, 1994
Low affinity heparin is an antithrombotic agent
E Gray, S Cesmeli, J C Lormeau, et al.
Seminars in Thrombosis and Hemostasis
|
January 1, 1994
Antithrombin: the principal inhibitor of thrombin
R J Olds, D A Lane, B Mille, et al.
The Journal of Biological Chemistry
|
November 25, 1994
Role of N- and C-terminal amino acids in antithrombin binding to pentasaccharide
B Mille, J Watton, T W Barrowcliffe, et al.
Acta Chirurgica Scandinavica. Supplementum
|
January 1, 1988
Equivalent effective doses of heparin and low molecular weight heparin(oid)s in haemodialysis for chronic renal failure
D A Lane, H Ireland, C J Tew, et al.
Blood
|
December 1, 1990
A frameshift mutation leading to type 1 antithrombin deficiency and thrombosis
R J Olds, D A Lane, G Finazzi, et al.
Page
of 27