Genetically determined variation in the complement system: relationship to disease (Q40182848)

18 September 2017

1 reference

title

Genetically determined variation in the complement system: relationship to disease (English)

1 reference

18 September 2017

McLean RH

1

1 reference

PubMed ID

6379135

18 September 2017

Winkelstein JA

series ordinal

2

1 reference

PubMed ID

6379135

18 September 2017

language of work or name

English

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publication date

1 August 1984

1 reference

The Journal of Pediatrics

18 September 2017

1 reference

18 September 2017

105

1 reference

18 September 2017

179-188

1 reference

18 September 2017

2

1 reference

Genetic polymorphism of the third component of human complement (C'3).

18 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

High voltage agarose gel electrophoresis in the study of C 3 polymorphism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Chido and Rodgers blood groups are distinct antigenic components of human complement C4.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Inherited structural polymorphism of the fourth component of human complement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Genetic polymorphism of human complement C4 and detection of heterozygotes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Genetic polymorphism of the third component of complement (C3) and levels of 1 C- 1 A-globulin in sera of German and Spanish populations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

7 January 2021

Polymorphism of human c5

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Genetic control of the eighth component of complement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Genetic polymorphism in human glycine-rich beta-glycoprotein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

On the significance of C2, C4, and factor B polymorphisms in disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

A molecular basis for the two locus model of human complement component C4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Capacity of complement c3 phenotypes to bind on to mononuclear cells in man.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Circulating immune complexes and glomerulonephritis in a patient with congenital absence of the third component of complement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Hereditary deficiency of the third component of complement in two sisters with systemic lupus erythematosus-like symptoms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Prevalence of congenital or acquired complement deficiency in patients with sporadic meningococcal disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Human deficiency of the eighth component of complement. The requirement of C8 for serum Neisseria gonorrhoeae bactericidal activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Identification of the alpha-gamma subunit of the eighth component of complement (C8) in a patient with systemic lupus erythematosus and absent C8 activity: patients and family studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Hereditary angioedema and “familial” lupus erythematosus in identical twin boys

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

HEREDITARY ANGIONEUROTIC EDEMA: TWO GENETIC VARIANTS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Biosynthetic Defect in Monocytes from Human Beings with Genetic Deficiency of the Second Component of Complement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Biosynthesis of the third component of complement (C3) in vitro by monocytes from both normal and homozygous C3-deficient humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Studies of a hypomorphic variant of human C3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Partial lipodystrophy and familial C3 deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Homozygous C3 deficiency: Detection of C3 by radioimmunoassay

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Partial H (beta 1H) deficiency and glomerulonephritis in two families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Inherited deficiency of the second component of complement. Rheumatic disease associations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implications

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Occurrence of an incomplete C8 molecule in homozygous C8 deficiency in man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

A genetic defect of the C1q subcomponent of complement associated with childhood (immune complex) nephritis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Complement-human histocompatibility antigen haplotypes in C2 deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Bf polymorphism: study of a new variant (F0.55)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Assignment of the structural gene for the third component of human complement to chromosome 19.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Activity of the alternative pathway of complement in the newborn infant

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Serum Complement Levels in Infancy: Age Related Changes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Serum complement profiles in infants and children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Family studies of complement C4 and HLA in man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

BF types and the mode of inheritance of insulin-dependent diabetes mellitus (IDDM)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Association between the C3F gene and atherosclerotic vascular diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Complement C4 is a marker for adult rheumatoid arthritis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Bf polymorphism and ankylosing spondylitis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Properdin factor B alleles in patients with idiopathic membranous nephropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

Complement deficiency states

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

inferred from DOI database lookup

7 January 2021

based on heuristic

Statement on the nomenclature of human C4 allotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

inferred from DOI database lookup

7 January 2021

based on heuristic

Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980110-9

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(84)80110-9

1 reference

18 September 2017

1 reference

PubMed ID

6379135