D N Cooper|D S Millar|A Wacey|S Pemberton|E G Tuddenham - JoVE Visualize

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British Journal of Haematology|June 1, 1993

A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiencyA I Wacey, S Pemberton, D N Cooper, et al.

British Medical Bulletin|October 1, 1994

Molecular genetics of familial venous thrombosisD N Cooper, E G Tuddenham

British Journal of Haematology|June 1, 1993

Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.

Human Genetics|September 1, 1996

Molecular reconstruction and homology modelling of the catalytic domain of the common ancestor of the haemostatic vitamin-K-dependent serine proteinasesM Krawczak, A Wacey, D N Cooper

British Journal of Rheumatology|May 1, 1995

Increase of activated factor VIIA and haemostatic molecular markers in juvenile chronic arthritisY Inamo, S Pemberton, E G Tuddenham, et al.

Human Genetics|October 6, 1998

Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNAD S Millar, M Krawczak, D N Cooper

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1994

Screening for inversions in the factor VIII (F8) gene causing severe haemophilia AD S Millar, V V Kakkar, D N Cooper

Blood|April 1, 1997

A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasminS Pemberton, P Lindley, V Zaitsev, et al.

Thrombosis and Haemostasis|April 1, 1994

Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia AD J Johnson, S Pemberton, M Acquila, et al.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994

A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.

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Showing results (1-10 of 317) with videos related to

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Pageof 32

British Journal of Haematology|June 1, 1993

A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiencyA I Wacey, S Pemberton, D N Cooper, et al.

British Medical Bulletin|October 1, 1994

Molecular genetics of familial venous thrombosisD N Cooper, E G Tuddenham

British Journal of Haematology|June 1, 1993

Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.

Human Genetics|September 1, 1996

Molecular reconstruction and homology modelling of the catalytic domain of the common ancestor of the haemostatic vitamin-K-dependent serine proteinasesM Krawczak, A Wacey, D N Cooper

British Journal of Rheumatology|May 1, 1995

Increase of activated factor VIIA and haemostatic molecular markers in juvenile chronic arthritisY Inamo, S Pemberton, E G Tuddenham, et al.

Human Genetics|October 6, 1998

Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNAD S Millar, M Krawczak, D N Cooper

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1994

Screening for inversions in the factor VIII (F8) gene causing severe haemophilia AD S Millar, V V Kakkar, D N Cooper

Blood|April 1, 1997

A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasminS Pemberton, P Lindley, V Zaitsev, et al.

Thrombosis and Haemostasis|April 1, 1994

Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia AD J Johnson, S Pemberton, M Acquila, et al.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994

A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.

Pageof 32