(Q36992143)

17 August 2017

Genetic polymorphism in C8 beta-chains. Evidence for two unlinked genetic loci for the eighth component of human complement (C8) (English)

1 reference

17 August 2017

C A Alper

1

1 reference

17 August 2017

D Marcus

2

1 reference

17 August 2017

D Raum

3

1 reference

17 August 2017

B H Petersen

4

1 reference

17 August 2017

T J Spira

5

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 November 1983

1 reference

Journal of Clinical Investigation

17 August 2017

1 reference

17 August 2017

72

1 reference

17 August 2017

5

1 reference

17 August 2017

1526-1531

1 reference

Sequential tests for the detection of linkage

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370440

Inherited structural polymorphism of 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=370440

Two types of dysfunctional eighth component of complement (C8) molecules in C8 deficiency in man. Reconstitution of normal C8 from the mixture of two abnormal C8 molecules

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370440

Occurrence of an incomplete C8 molecule in homozygous C8 deficiency 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=370440

Recurrent meningococcal infections associated with a functional deficiency of the C8 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=370440

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=370440

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=370440

The membrane attack mechanism of complement: the three polypeptide chain structure of the eigth component (C8)

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370440

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=370440

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=370440

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=370440

Genetic control of the eighth 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=370440

International system for human gene nomenclature (1979) ISGN (1979).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370440

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=370440

Haptoglobin "Marburg"; studies on a rare hereditary haptoglobin variant with 2 different phenotypes in one family

29 September 2017

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6415112

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A familial dysfunction of the eight component of complement (C8)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6415112

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The eighth component of human complement. Purification and physicochemical characterization of its unusual subunit structure

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6415112

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI111111

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

6415112

1 reference