Synthesis of C1 inhibitor in fibroblasts from patients with type I and type II hereditary angioneurotic edema (Q34187487)

31 July 2017

title

Synthesis of C1 inhibitor in fibroblasts from patients with type I and type II hereditary angioneurotic edema (English)

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31 July 2017

J Kramer

1

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31 July 2017

Y Katz

2

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31 July 2017

F S Rosen

3

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31 July 2017

A E Davis

4

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31 July 2017

R C Strunk

5

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31 July 2017

language of work or name

English

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publication date

1 May 1991

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Journal of Clinical Investigation

31 July 2017

published in

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31 July 2017

volume

87

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31 July 2017

issue

5

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31 July 2017

page(s)

1614-1620

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Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Variability in purified dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema. Functional and analytical gel studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Demonstration of modified inactive first component of complement (C1) inhibitor in the plasmas of C1 inhibitor-deficient patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Dysfunctional C1-inhibitor(At), isolated from a type II hereditary-angio-oedema plasma, contains a P1 'reactive centre' (Arg444----His) mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Synergism between gamma interferon and lipopolysaccharide for synthesis of factor B, but not C2, in human fibroblasts

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Synthesis and regulation of C1 inhibitor in human skin fibroblasts

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Identification of a serpin-enzyme complex receptor on human hepatoma cells and human monocytes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Hormonal regulation of complement biosynthesis in human cell lines--II. Upregulation of the biosynthesis of complement components C3, factor B and C1 inhibitor by interleukin-6 and interleukin-1 in human hepatoma cell line.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation site

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implications

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295244

Interactions of plasma kallikrein and C1-s with normal and dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema: analytic gel studies

5 July 2018

1 reference

12 December 2020

gamma-Interferon increases expression of class III complement genes C2 and factor B in human monocytes and in murine fibroblasts transfected with human C2 and factor B genes

1 reference

12 December 2020

Interferon-gamma is a major regulator of C1-inhibitor synthesis by human blood monocytes

1 reference

12 December 2020

Synovial fibroblast-like cells synthesize seven proteins of the complement system

1 reference

12 December 2020

Synthesis and expression of C1 inhibitor by human umbilical vein endothelial cells

1 reference

12 December 2020

Monocyte C1-inhibitor synthesis in patients with C1-inhibitor deficiency

1 reference

12 December 2020

Altered C1 inhibitor genes in type I hereditary angioedema

1 reference

12 December 2020

The catabolism of C1(-)-inhibitor and the pathogenesis of hereditary angio-edema

1 reference

12 December 2020

Tissue-specific pretranslational regulation of complement production in human mononuclear phagocytes

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI115175

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31 July 2017

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31 July 2017

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