(Q33762493)

29 July 2017

1 reference

title

Properdin deficiency and meningococcal disease--identifying those most at risk (English)

1 reference

29 July 2017

1 reference

S M Linton

1

1 reference

PubMed ID

10540177

29 July 2017

B P Morgan

series ordinal

2

1 reference

PubMed ID

10540177

29 July 2017

language of work or name

1 reference

1 November 1999

1 reference

Clinical and Experimental Immunology

29 July 2017

1 reference

29 July 2017

118

1 reference

29 July 2017

2

1 reference

29 July 2017

189-191

1 reference

Complement deficiency and disease

29 July 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Chromosomal translocations in lymphoid malignancies reveal novel proto-oncogenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Properdin: binding to C3b and stabilization of the C3b-dependent C3 convertase

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Properdin, the terminal complement components, thrombospondin and the circumsporozoite protein of malaria parasites contain similar sequence motifs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

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/10.1046%2FJ.1365-2249.1999.01057.X

Genetic and physical mapping around the properdin P gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Human properdin deficiency has a heterogeneous genetic background

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Infectious diseases associated with complement deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Congenital properdin deficiency and meningococcal infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Dysfunctional properdin in a Dutch family with meningococcal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Hereditary properdin deficiency in three families of Tunisian Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Killing of Neisseria meningitidis by human neutrophils: implications for normal and complement-deficient individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Protection against meningococcal serogroup ACYW disease in complement-deficient individuals vaccinated with the tetravalent meningococcal capsular polysaccharide vaccine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Vaccination against meningococcus in complement-deficient individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Correlation between G2m(n) immunoglobulin allotype and human antibody response and susceptibility to polysaccharide encapsulated bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2249.1999.01057.X

Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.

21 January 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905414

Properdin deficiency in a family with fulminant meningococcal infections.

30 October 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905414

Inherited complement deficiency states: implications for immunity and immunological disease

30 October 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905414

Analysis of the natural polymeric forms of human properdin and their functions in complement activation

30 October 2018

1 reference

12 December 2020

Polymorphism of IgG Fc receptors in meningococcal disease

1 reference

12 December 2020

Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families

1 reference

12 December 2020

Assessment of complement deficiency in patients with meningococcal disease in The Netherlands

1 reference

12 December 2020

Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)

1 reference

12 December 2020

Genes Associated with the G2m(23) Immunoglobulin Allotype Regulate the IgG Subclass Responses to Haemophilus influenzae Type b Polysaccharide Vaccine

1 reference

12 December 2020

10.1046/J.1365-2249.1999.01057.X

Identifiers

DOI

1 reference

release_7dc75muwgrhhjetcuryldymaem

29 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7dc75muwgrhhjetcuryldymaem

24 November 2022

mapped directly with Wikidata item

0 references

1 reference

PubMed ID

10540177