Restricted genetic defects underlie human complement C6 deficiency (Q56966176)

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Language	Label	Description	Also known as
English	Restricted genetic defects underlie human complement C6 deficiency	No description defined

Statements

scholarly article

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Restricted genetic defects underlie human complement C6 deficiency (English)

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author name string

M A Dragon-Durey

1

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V Fremeaux-Bacchi

2

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J Blouin

3

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D Barraud

4

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W H Fridman

5

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M D Kazatchkine

6

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language of work or name

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publication date

April 2003

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Clinical and Experimental Immunology

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132

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1

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87-91

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Complement. First of two parts

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

Complement. Second of two parts

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

Complement membrane attack on nucleated cells: resistance, recovery and non-lethal effects

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

Role of the C5b-9 complement complex in cell cycle and apoptosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

The membrane attack complex of complement induces caspase activation and apoptosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

High prevalence of complement component C6 deficiency among African-Americans in the south-eastern USA.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2003.02099.X

21 January 2018

Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Structure of the human C6 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Effect of cytokines on the secretion of the fifth and eighth complement components by HepG2 cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

A rapid method for the purification of DNA from blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Arthritis and antinuclear antibodies (ANA) with inherited deficiency of the sixth component of complement (C6).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Inherited deficiencies of the terminal components of human complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1808670

2 November 2018

Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/12653841

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A lupus-like syndrome in a patient with deficiency of the sixth component of complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/12653841

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary complement (C6) deficiency associated with systemic lupus erythematosus, Sjögren's syndrome and hyperthyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/12653841

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high incidence of C9 deficiency among healthy blood donors in Osaka, Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/12653841

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular defects leading to human complement component C6 deficiency in an African-American family

1 reference

https://pubmed.ncbi.nlm.nih.gov/12653841

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of C6 deficiency in the western Cape, South Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/12653841

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1046/J.1365-2249.2003.02099.X

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PubMed publication ID

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