C1r deficiency: an inborn error associated with cutaneous and renal disease. - Wikidata - wikimedia - TriplyDB

C1r deficiency: an inborn error associated with cutaneous and renal disease.

C1r deficiency: an inborn error associated with cutaneous and renal disease.

http://www.wikidata.org/entity/Q34068956

about

Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases The glomerular mesangium. II. Studies of macromolecular uptake in nephrotoxic nephritis in rats.Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studies.Complete absence of the third component of complement in man.The complement system in bullous pemphigoid. I. Complement and component levels in sera and blister fluids.C2 deficiency. Development of lupus erythematosus The association of respiratory infection, recurrent hematuria, and focal glomerulonephritis with activation of the complement system in the cold.A new complement-mediated cytolytic mechanism--the C1-bypass activation pathway.The genetic and molecular bases of monogenic disorders affecting proteolytic systems.Familial cutaneous lupus erythematosus (CLE) in the German shorthaired pointer maps to CFA18, a canine orthologue to human CLE Inherited deficiency of the second component of complement. Rheumatic disease associations.Genetic deficiencies of the complement system and association with disease--early components.Biological mechanism analysis of acute renal allograft rejection: integrated of mRNA and microRNA expression profiles.Complement activation in pemphigus vulgaris blister fluid.

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P2860

C1r deficiency: an inborn error associated with cutaneous and renal disease.

http://www.wikidata.org/entity/Q34068956

description

1972 nî lūn-bûn

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1972 թուականի Մայիսին հրատարակուած գիտական յօդուած

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1972 թվականի մայիսին հրատարակված գիտական հոդված

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1972年の論文

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1972年論文

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1972年論文

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1972年論文

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1972年論文

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1972年論文

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1972年论文

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name

C1r deficiency: an inborn error associated with cutaneous and renal disease.

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C1r deficiency: an inborn error associated with cutaneous and renal disease.

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C1r deficiency: an inborn error associated with cutaneous and renal disease.

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type

label

C1r deficiency: an inborn error associated with cutaneous and renal disease.

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C1r deficiency: an inborn error associated with cutaneous and renal disease.

@en

C1r deficiency: an inborn error associated with cutaneous and renal disease.

@nl

prefLabel

C1r deficiency: an inborn error associated with cutaneous and renal disease.

@ast

C1r deficiency: an inborn error associated with cutaneous and renal disease.

@en

C1r deficiency: an inborn error associated with cutaneous and renal disease.

@nl

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Journal of Clinical Investigation

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C1r deficiency: an inborn error associated with cutaneous and renal disease.

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P2093

Day NK

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DeBracco M

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Geiger H

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Good RA

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Mancaido B

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Stroud R

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Windhorst D

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P2860

Immunochemical quantitation of antigens by single radial immunodiffusion

Methods for the separation, purification and measurement of nine components of hemolytic complement in guinea-pig serum

C1r, subunit of the first complement component: purification, properties, and assay based on its linking role.

IMMUNOLOGICAL STUDIES OF THE 11S PROTEIN COMPONENT OF THE HUMAN COMPLEMENT SYSTEM

The enzymatic nature of C'1r. Conversion of C'1s to C'1 esterase and digestion of amino acid esters by C'1r

Interactions of the complement system with endotoxic lipopolysaccharide: consumption of each of the six terminal complement components

Deficiency of C1r in human serum. Effects on the structure and function of macromolecular C1.

Complement and complement-like activity in lower vertebrates and invertebrates.

An alternate complement pathway: C-3 cleaving activity, not due to C4,2a, on endotoxic lipopolysaccharide after treatment with guinea pig serum; relation to properdin.

Complement and complement component activities in diseases associated with repeated infections and malignancy.

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1102-1108

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10.1172/JCI106902

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18543436

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4623164

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292239

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