L K Jones|E G Tuddenham - JoVE Visualize

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British Journal of Haematology|October 1, 1995

Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacsR Schwaab, J Oldenburg, U Schwaab, et al.

Blood|July 29, 1998

Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiencyJ H McVey, E J Boswell, O Takamiya, et al.

British Journal of Haematology|May 31, 2001

Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM(-)) and G1948D (CRM(r))D David, E L Saenko, I M Santos, et al.

Nature|May 5, 1985

Detection and sequence of mutations in the factor VIII gene of haemophiliacsJ Gitschier, W I Wood, E G Tuddenham, et al.

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.

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

Haemophilia A diagnosis by automated fluorescent DNA detection of ten factor VIII intron 13 dinucleotide repeat allelesL Kochhan, M R Lalloz, J Oldenburg, et al.

Blood|March 1, 1982

Preparation of factor IX deficient human plasma by immunoaffinity chromatography using a monoclonal antibodyA H Goodall, G Kemble, D P O'Brien, et al.

Thrombosis and Haemostasis|December 1, 1995

Haemophilia A: mutation type determines risk of inhibitor formationR Schwaab, H H Brackmann, C Meyer, et al.

Human Genetics|January 24, 1998

Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII proteinR Schwaab, J Oldenburg, M R Lalloz, et al.

Blood|July 1, 1991

Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected maleD P O'Brien, K M Gale, J S Anderson, et al.

Pageof 14

Showing results (91-100 of 135) with videos related to

Sort By:

Pageof 14

British Journal of Haematology|October 1, 1995

Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacsR Schwaab, J Oldenburg, U Schwaab, et al.

Blood|July 29, 1998

Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiencyJ H McVey, E J Boswell, O Takamiya, et al.

British Journal of Haematology|May 31, 2001

Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM(-)) and G1948D (CRM(r))D David, E L Saenko, I M Santos, et al.

Nature|May 5, 1985

Detection and sequence of mutations in the factor VIII gene of haemophiliacsJ Gitschier, W I Wood, E G Tuddenham, et al.

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.

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

Haemophilia A diagnosis by automated fluorescent DNA detection of ten factor VIII intron 13 dinucleotide repeat allelesL Kochhan, M R Lalloz, J Oldenburg, et al.

Blood|March 1, 1982

Preparation of factor IX deficient human plasma by immunoaffinity chromatography using a monoclonal antibodyA H Goodall, G Kemble, D P O'Brien, et al.

Thrombosis and Haemostasis|December 1, 1995

Haemophilia A: mutation type determines risk of inhibitor formationR Schwaab, H H Brackmann, C Meyer, et al.

Human Genetics|January 24, 1998

Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII proteinR Schwaab, J Oldenburg, M R Lalloz, et al.

Blood|July 1, 1991

Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected maleD P O'Brien, K M Gale, J S Anderson, et al.

Pageof 14