Identification of a new P1 residue mutation (444Arg----Ser) in a dysfunctional C1 inhibitor protein contained in a type II hereditary angioedema plasma (Q24339566)

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Language	Label	Description	Also known as
English	Identification of a new P1 residue mutation (444Arg----Ser) in a dysfunctional C1 inhibitor protein contained in a type II hereditary angioedema plasma	scientific article

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scholarly article

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Identification of a new P1 residue mutation (444Arg----Ser) in a dysfunctional C1 inhibitor protein contained in a type II hereditary angioedema plasma (English)

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Serpin family G member 1

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GOA release 2020-03-11

blood circulation

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GOA release 2020-03-11

hereditary angioedema

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based on heuristic

inferred from title

author name string

K S Aulak

1

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M Cicardi

2

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R A Harrison

3

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language of work or name

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publication date

18 June 1990

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266

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1-2

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13-6

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Interaction of 125I-labelled complement subcomponents C-1r and C-1s with protease inhibitors in plasma

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Inactivation of factor XII active fragment in normal plasma. Predominant role of C-1-inhibitor

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Contribution of Plasma Protease Inhibitors to the Inactivation of Kallikrein in Plasma

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Inactivation of kallikrein in human plasma

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The inhibition of plasmin, plasma kallikrein, plasma permeability factor, and the C'1r subcomponent of the first component of complement by serum C'1 esterase inhibitor

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A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE.

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HEREDITARY ANGIONEUROTIC EDEMA: TWO GENETIC VARIANTS.

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Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.

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The covalent nature of the human antithrombin III--thrombin bond

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Alpha-1-antitrypsin-Pittsburgh. A potent inhibitor of human plasma factor XIa, kallikrein, and factor XIIf

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A simplified method for cyanogen bromide activation of agarose for affinity chromatography

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Dysfunctional C1-inhibitor(At), isolated from a type II hereditary-angio-oedema plasma, contains a P1 'reactive centre' (Arg444----His) mutation

1 reference

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The structural basis for neutrophil inactivation of C1 inhibitor.

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Type II hereditary angioneurotic edema that may result from a single nucleotide change in the codon for alanine-436 in the C1 inhibitor gene

1 reference

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C1 inhibitor and hereditary angioneurotic edema

1 reference

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Hereditary angioneurotic edema. II. Deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikrein

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Altered specificities of genetically engineered alpha 1 antitrypsin variants

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Human C1 inhibitor: improved isolation and preliminary structural characterization

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Antithrombin III Glasgow: a variant with increased heparin affinity and reduced ability to inactivate thrombin, associated with familial thrombosis

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Cloning and expression of the cDNA for human antithrom, bin III

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Identifiers

10.1016/0014-5793(90)81494-9

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