Genetic deficiencies of the complement system and association with disease--early components (Q40829860)

24 September 2017

1 reference

title

Genetic deficiencies of the complement system and association with disease--early components (English)

1 reference

24 September 2017

Kölble K

1

1 reference

PubMed ID

8340675

24 September 2017

Reid KB

series ordinal

2

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24 September 2017

1 January 1993

1 reference

International Reviews of Immunology

24 September 2017

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24 September 2017

10

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24 September 2017

1

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24 September 2017

17-36

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Circular-dichroism and electron-microscopy studies of human subcomponent C1q before and after limited proteolysis by pepsin

24 September 2017

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Characterization and organization of the genes encoding the A-, B- and C-chains of human complement subcomponent C1q. The complete derived amino acid sequence of human C1q

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Molecular cloning and characterization of the complementary DNA and gene coding for the B-chain of subcomponent C1q of the human complement system

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Activation of the first component of complement

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

The first component of complement. A quantitative comparison of its biosynthesis in culture by human epithelial and mesenchymal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Deficiency of C1r in human serum. Effects on the structure and function of macromolecular C1.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Nucleotide sequence of the cDNA coding for human complement C1r

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Complete cDNA sequence of human complement Cls and close physical linkage of the homologous genes Cls and Clr.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Human genes for complement components C1r and C1s in a close tail-to-tail arrangement

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

High resolution electrophoresis for the allotyping of human C4. Proposal of a relational nomenclature.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

The structural basis of the multiple forms of human complement component C4.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Polymorphism of human complement component C4.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

The chemical structure of the C4d fragment of the human complement component C4.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Molecular mapping of the human major histocompatibility complex by pulsed-field gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Direct observation of the gene organization of the complement C4 and 21-hydroxylase loci by pulsed field gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Definitive RFLPs to distinguish between the human complement C4A/C4B isotypes and the major Rodgers/Chido determinants: application to the study of C4 null alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Cell-specific expression of the human complement protein factor B gene: evidence for the role of two distinct 5'-flanking elements

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

DNA polymorphism of the C2 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Increased risk of neisserial infections in systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

The properdin system and immunity. I. Demonstration and isolation of a new serum protein, properdin, and its role in immune phenomena

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Molecular cloning of the cDNA coding for properdin, a positive regulator of the alternative pathway of human complement

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Genetic and physical mapping around the properdin P gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Congenital properdin deficiency and meningococcal infection

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Dysfunctional properdin in a Dutch family with meningococcal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Familial properdin deficiency and fatal meningococcemia. Correction of the bactericidal defect by vaccination

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Another Swedish family with complete properdin deficiency: association with fulminant meningococcal disease in one male family member

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Adipsin and complement factor D activity: an immune-related defect in obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Haemolytic diffusion plate assays for factors B and D of the alternative pathway of complement activation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

The factor B and C2 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

A new TaqI polymorphism of the complement factor B gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Recurrent septicemia associated with congenital deficiency of C2 and partial deficiency of factor B and the alternative complement pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

A hemolytically inactive gene product of factor B.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

C1r deficiency: an inborn error associated with cutaneous and renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Familial deficiency of two subunits of the first component of complement. C1r and C1s associated with a lupus erythematosus-like disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Inborn Clr deficiency with a mild lupus-like syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

Recurrent infections and staphylococcal liver abscess in a child with C1r deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F08830189309051169

10.3109/08830189309051169

21 January 2018

Identifiers

DOI

1 reference

24 September 2017

1 reference

PubMed ID

8340675