(Q69637409)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2736801%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

title

Familial properdin deficiency associated with chronic discoid lupus erythematosus (English)

1 reference

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4 October 2019

1 reference

1 reference

Holme ER

1

1 reference

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4 October 2019

Veitch J

2

1 reference

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4 October 2019

Johnston A

3

1 reference

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4 October 2019

Hauptmann G

4

1 reference

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4 October 2019

Uring-Lambert B

5

1 reference

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4 October 2019

Seywright M

6

1 reference

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4 October 2019

Docherty V

7

1 reference

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4 October 2019

Morley WN

8

1 reference

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4 October 2019

Whaley K

9

1 reference

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4 October 2019

publication date

1 April 1989

1 reference

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Clinical and Experimental Immunology

4 October 2019

published in

1 reference

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4 October 2019

volume

76

1 reference

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4 October 2019

issue

1

1 reference

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4 October 2019

page(s)

76-81

1 reference

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Genetic polymorphism in human glycine-rich beta-glycoprotein

4 October 2019

cites work

1 reference

12 December 2020

Precise Standardization of Reagents for Complement Fixation

1 reference

12 December 2020

Enhancing role of IgG in lysis of rabbit erythrocytes by the alternative pathway of human complement

1 reference

12 December 2020

Inherited structural polymorphism of the fourth component of human complement

1 reference

12 December 2020

Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

1 reference

12 December 2020

Properdin deficiency in a family with fulminant meningococcal infections.

1 reference

12 December 2020

Complement-mediated inhibition of immune precipitation in patients with immune complex diseases

1 reference

12 December 2020

Complement, the immune-complex lattice, and the pathophysiology of complement-deficiency syndromes

1 reference

12 December 2020

Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency

1 reference

12 December 2020

Selective depression of the C4 component of complement: evidence for an association with genetic deficiency of C4 and dermatologic diseases

1 reference

12 December 2020

Familial discoid lupus erythematosus associated with heterozygous C4 deficiency

1 reference

12 December 2020

Formation of soluble immune complexes by complement in sera of patients with various hypocomplementemic states. Difference between inhibition of immune precipitation and solubilization

1 reference

12 December 2020

Detection of the genetic polymorphism of human C2 (native protein and C2a fragment) by immunoblotting after polyacrylamide gel isoelectric focusing

1 reference

12 December 2020

Familial properdin deficiency and fatal meningococcemia. Correction of the bactericidal defect by vaccination

1 reference

12 December 2020

Inherited deficiency of properdin and C2 in a patient with recurrent bacteremia

1 reference

12 December 2020

Phenotyping of human complement component C4, a class-III HLA antigen

1 reference

12 December 2020

Congenital properdin deficiency and meningococcal infection

1 reference

12 December 2020

The IgA-binding lectin jacalin induces complement activation by inhibition of C-1-inactivator function

1 reference

12 December 2020

Quantitation of human C4A and C4B, in serum and plasma by enzyme-linked immunoadsorbent assay

1 reference

12 December 2020

Purification of a plasma protein that inhibits complement-mediated prevention of immune precipitation

1 reference

12 December 2020

Properdin factor D. II. Activation to D by properdin

1 reference

12 December 2020

Identifiers

1 reference