(Q34618262)

English

Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens

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scholarly article

1 reference

Europe PubMed Central

3 August 2017

Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens (English)

1 reference

Europe PubMed Central

3 August 2017

author name string

W A Muir

1

1 reference

Europe PubMed Central

3 August 2017

S Hedrick

2

1 reference

Europe PubMed Central

3 August 2017

C A Alper

3

1 reference

Europe PubMed Central

3 August 2017

O D Ratnoff

4

1 reference

Europe PubMed Central

3 August 2017

B Schacter

5

1 reference

Europe PubMed Central

3 August 2017

J J Wisnieski

6

1 reference

Europe PubMed Central

3 August 2017

language of work or name

0 references

publication date

1 October 1984

1 reference

Europe PubMed Central

3 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

3 August 2017

74

1 reference

Europe PubMed Central

3 August 2017

1509-1514

1 reference

Europe PubMed Central

3 August 2017

4

1 reference

Europe PubMed Central

3 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Clot retraction as a measure of platelet function. II. Clinical disorders associated with qualitative platelet defects (thrombocytopathic purpura).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Genetic analysis of C4 deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Inherited structural polymorphism of the fourth component of human complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Methods for the separation, purification and measurement of nine components of hemolytic complement in guinea-pig serum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Clues to the pathogenesis of bleeding in von Willebrand's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Detection of immune complexes in unheated sera by modified 125I-Clq binding test. Effect of heating on the binding of Clq by immune complexes and application of the test to systemic lupus erythematosus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Polymorphism of red cell glyoxalase I (EI: 4.4.1.5); a new genetic marker in man. Investigation of 169 mother-child combinations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Hereditary C4 deficiency--genetic studies and linkage to HLA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Improved B Cell Typing for HLA-DR Using Nylon Wool Column Enriched B Lymphocyte Preparations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425321

7 July 2018

Selective deficiency of the fourth component of complement in a patient with systemic lupus erythematosus (SLE): immunochemical and biological studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systemic lupus erythematosus in a patient with C4 deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systemic lupus erythematosus in hereditary deficiency of the fourth component of complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic deficiency of C4 presenting with recurrent infections and a SLE-like disease. Genetic and immunologic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MEASUREMENT OF PLATELET ADHESIVENESS. A SIMPLE IN VITRO TECHNIQUE DEMONSTRATING AN ABNORMALITY IN VON WILLEBRAND'S DISEASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

STUDIES ON PLATELET FACTOR-3 AVAILABILITY

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An inherited qualitative abnormality in plasma fibrinogen: fibrinogen Cleveland

1 reference

https://pubmed.ncbi.nlm.nih.gov/6480834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI111564

1 reference

Europe PubMed Central

3 August 2017

release_246mwpipe5gepbumq2rzqd4g3y

1 reference

https://api.fatcat.wiki/v0/release/246mwpipe5gepbumq2rzqd4g3y

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

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