Genetic control of the eighth component of complement (Q37041890)

17 August 2017

Genetic control of the eighth component of complement (English)

1 reference

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4 July 2022

author name string

D. Raum

1

1 reference

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4 July 2022

M. A. Spence

2

1 reference

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4 July 2022

D. Balavitch

3

1 reference

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4 July 2022

S. Tideman

4

1 reference

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4 July 2022

A. D. Merritt

5

1 reference

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4 July 2022

R. T. Taggart

6

1 reference

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4 July 2022

B. H. Petersen

7

1 reference

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4 July 2022

N. K. Day

8

1 reference

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4 July 2022

C. A. Alper

9

1 reference

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4 July 2022

language of work or name

English

0 references

publication date

1 September 1979

1 reference

PMCID

372192

full work available at URL

17 August 2017

https://europepmc.org/articles/PMC372192

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468996

https://europepmc.org/articles/PMC372192?pdf=render

4 July 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468996

Journal of Clinical Investigation

4 July 2022

published in

1 reference

17 August 2017

64

1 reference

17 August 2017

3

1 reference

17 August 2017

858-865

1 reference

Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studies

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Inherited deficiency of the third component of human complement (C′3)

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Genetic polymorphism in human glycine-rich beta-glycoprotein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Data on the HL-A linkage group

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Hereditary C2 deficiency: Genetic studies and association with the HL-A system

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

The genetic polymorphism of the fourth component of human complement: methodological aspects and a presentation of linkage and association data relevant to its localization in the HLA region

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Absence of the eighth component of complement in association with systemic lupus erythematosus-like disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Allotypes of complement components in man

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Hereditary deficiency of the fifth component of complement in man. II. Biological properties of C5-deficient human serum

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Two HLA-linked loci controlling the fourth component of human complement

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Mapping of the structural gene for the second component of complement with respect to the human major histocompatibility complex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Homozygous C3 deficiency: Detection of C3 by radioimmunoassay

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

C8 deficiency in a family with xeroderma pigmentosum. Lack of linkage to the HLA region

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Linkage between the Gene (or Genes) Controlling Synthesis of the Fourth Component of Complement and the Major Histocompatibility Complex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Lack of linkage between gene(s) controlling the synthesis of the seventh component of complement and the HLA region on chromosome No. 6 in man

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Combined genetic deficiency of C6 and C7 in man

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Association between hla and cutaneous necrotizing venulitis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

One cell-one immunoglobulin. Origin of limited heterogeneity of myeloma proteins

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Molecular analysis of the membrane attack mechanism of complement

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Isoelectric focusing in polyacrylamide gel and its application to immunoglobulins

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Inherited structural variation and linkage relationships of C7

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Inherited deficiency of the sixth component of complement: a silent or null gene

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=372192

Evidence for a silent or null gene in hereditary C2 deficiency

27 June 2018

1 reference

12 December 2020

Linkage studies with C6

1 reference

12 December 2020

Genetics of the complement system

1 reference

12 December 2020

Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA).

1 reference

12 December 2020

Homozygous deficiency of C3 in a patient with repeated infections

1 reference

12 December 2020

Genetic polymorphism of C'3(beta1C-globulin) in human serum

1 reference

12 December 2020

Linkage of HL-A and GBG

1 reference

12 December 2020

C3 polymorphism: genetic linkage relations

1 reference

12 December 2020

Hereditary C2 deficiency: diagnosis and HLA gene complex associations

1 reference

12 December 2020

Serotyping for homotransplantation. 18. Refinement of microdroplet lymphocyte cytotoxicity test

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI109534

1 reference

17 August 2017

1 reference

17 August 2017

1 reference

PMCID

372192