(Q46689431)

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Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family

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scholarly article

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family (English)

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

systemic lupus erythematosus

1 reference

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inferred from title

author name string

V Fremeaux-Bacchi

1

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

B Uring-Lambert

2

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

L Weiss

3

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

P Brun

4

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

J Blouin

5

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

D Hartmann

6

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

C Loirat

7

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

G Hauptmann

8

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

M D Kazatchkine

9

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

publication date

1 September 1994

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

Journal of Clinical Immunology

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

14

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24 December 2017

http://europepmc.org/abstract/MED/7814456

5

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

273-279

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

https://scigraph.springernature.com/pub.10.1007/bf01540980

0 references

Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Hereditary deficiency of the 4th component of complement (C4) associated with a lupic syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary complete deficiency of the fourth component of complement: effects on the kidney

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of high-molecular-weight DNA from mammalian cells

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https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of complete C4 deficiency. A study of three patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparison of the properties of two classes, C4A and C4B, of the human complement component C4

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental isodisomy 6 associated with deficiency of the fourth component of complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Revised nomenclature for human complement component C4. WHO-IUIS Nomenclature Sub-Committee

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https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal disease in a patient with hereditary complete deficiency of the fourth component of complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of HLA-DR oligotyping to 110 kidney transplant patients with doubtful serological typing

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Difference in the biological properties of the two forms of the fourth component of human complement (C4)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited structural polymorphism of the fourth component of human complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of the genetic polymorphism of human C2 (native protein and C2a fragment) by immunoblotting after polyacrylamide gel isoelectric focusing

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement deficiency: predisposing factor to autoimmune syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microdroplet Assay of Human Serum Cytotoxins

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01540980

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

release_x43nvs73lnb4za7xy6tjhsipea

1 reference

https://api.fatcat.wiki/v0/release/x43nvs73lnb4za7xy6tjhsipea

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/7814456

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