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

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scientific article published on August 1984

Language	Label	Description	Also known as
English	Genetically determined variation in the complement system: relationship to disease	scientific article published on August 1984

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

1 reference

Europe PubMed Central

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

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

author name string

McLean RH

1

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Winkelstein JA

2

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

language of work or name

0 references

publication date

1 August 1984

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

105

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

179-188

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Inherited structural polymorphism of the fourth component of human complement

1 reference

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

7 January 2021

Genetic polymorphism of human complement C4 and detection of heterozygotes

1 reference

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

7 January 2021

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

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

7 January 2021

Genetic control of the eighth component of complement

1 reference

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

7 January 2021

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

HEREDITARY ANGIONEUROTIC EDEMA: TWO GENETIC VARIANTS.

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Studies of a hypomorphic variant of human C3

1 reference

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

7 January 2021

Partial lipodystrophy and familial C3 deficiency

1 reference

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

7 January 2021

Homozygous C3 deficiency: Detection of C3 by radioimmunoassay

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Complement-human histocompatibility antigen haplotypes in C2 deficiency

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Activity of the alternative pathway of complement in the newborn infant

1 reference

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

7 January 2021

Serum Complement Levels in Infancy: Age Related Changes

1 reference

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

7 January 2021

Serum complement profiles in infants and children

1 reference

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

7 January 2021

Family studies of complement C4 and HLA in man

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Association between the C3F gene and atherosclerotic vascular diseases

1 reference

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

7 January 2021

Complement C4 is a marker for adult rheumatoid arthritis

1 reference

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

7 January 2021

Bf polymorphism and ankylosing spondylitis

1 reference

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

7 January 2021

Properdin factor B alleles in patients with idiopathic membranous nephropathy

1 reference

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

7 January 2021

Complement deficiency states

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Statement on the nomenclature of human C4 allotypes

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0022-3476(84)80110-9

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

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