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Molecular defects in hereditary angioneurotic edema.

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Antibody to C1-inhibitor in a patient receiving C1-inhibitor infusions for treatment of hereditary angioneurotic edema with systemic lupus erythematosus reacts with a normal allotype of residue 458 of C1-inhibitor.

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An autoantibody to C1-inhibitor recognizes the reactive center of the inhibitor.

The Journal of laboratory and clinical medicine·1996

A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.

Proceedings of the National Academy of Sciences of the United States of America·1994

Contiguous deletion and duplication mutations resulting in type 1 hereditary angioneurotic edema.

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Complement activation characterizes a high mortality subgroup in pulmonary embolism: An observational proteomic study.

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The calf clot of the lungs: Detection, overdiagnosis, and structured surveillance in isolated subsegmental pulmonary embolism.

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Fibrinogen activity and postpartum hemorrhage risk in women with congenital fibrinogen disorders: A multicenter real-world study.

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The Factor VII mutation F7 c.760T>C (FVIIp.Cys254Arg) is causative for Factor VII deficiency by impairing secretion.

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An Ion-Neutral Reaction to Form Cyanobenzene and Ethynylbenzene in Titan's Atmosphere.

ACS earth & space chemistry·2026

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Potassium-Concentration-Gated C-N Coupling Enables a Volcano-Shaped Selectivity Window for Electrocatalytic Urea Synthesis.

Angewandte Chemie (International ed. in English)·2026

Experimental phyllotactic patterns in the wake of radially moving chemical precipitation fronts.

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Related Experiment Videos

The role of plasmin in kinin-release by preparations of human thrombin

Related Concept Videos

An HMG-I protein from human endothelial cells apparently is secreted and impairs activation of Hageman factor (factor XII).

Molecular defects in hereditary angioneurotic edema.

Antibody to C1-inhibitor in a patient receiving C1-inhibitor infusions for treatment of hereditary angioneurotic edema with systemic lupus erythematosus reacts with a normal allotype of residue 458 of C1-inhibitor.

An autoantibody to C1-inhibitor recognizes the reactive center of the inhibitor.

A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.

Contiguous deletion and duplication mutations resulting in type 1 hereditary angioneurotic edema.

Complement activation characterizes a high mortality subgroup in pulmonary embolism: An observational proteomic study.

The calf clot of the lungs: Detection, overdiagnosis, and structured surveillance in isolated subsegmental pulmonary embolism.

Perioperative haemostatic management and bleeding outcomes in congenital factor VII deficiency: a retrospective cohort study.

Fibrinogen activity and postpartum hemorrhage risk in women with congenital fibrinogen disorders: A multicenter real-world study.

The Factor VII mutation F7 c.760T>C (FVIIp.Cys254Arg) is causative for Factor VII deficiency by impairing secretion.

A human-cell recombinant prethrombin-2 platform producing thrombin with enhanced fibrinogen processing for in vitro applications.

An Ion-Neutral Reaction to Form Cyanobenzene and Ethynylbenzene in Titan's Atmosphere.

Postsurgical Carpal Collapse Following Scaphoidectomy With Partial Wrist Fusion: A Retrospective Radiographic Study.

Photoredox Catalysis by Phosphorus(V)-Corrole: α-Functionalization of Aldehydes in both Batch and Continuous Flow Conditions.

Potassium-Concentration-Gated C-N Coupling Enables a Volcano-Shaped Selectivity Window for Electrocatalytic Urea Synthesis.

Experimental phyllotactic patterns in the wake of radially moving chemical precipitation fronts.

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The role of plasmin in kinin-release by preparations of human thrombin

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