(Q73128888)

English

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)

scientific article published on 01 November 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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) (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

meningococcal disease

1 reference

based on heuristic

inferred from title

properdin deficiency

1 reference

based on heuristic

inferred from title

author name string

P J Späth

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

A G Sjöholm

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

G N Fredrikson

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

G Misiano

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

R Scherz

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

U B Schaad

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

B Uhring-Lambert

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

G Hauptmann

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J Westberg

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

M Uhlén

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

C Wadelius

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

L Truedsson

12

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

publication date

1 November 1999

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Clinical and Experimental Immunology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

118

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

278-284

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10540191%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

The role of complement in inflammation and phagocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of mannan binding protein--a new complement deficiency syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thymus-independent and thymus-dependent responses to polysaccharide antigens

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis in properdin deficiency families: refined location in proximal Xp

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum IgG and IgG subclass contents in different Gm phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum bactericidal activity and induction of chemiluminescence of polymorphonuclear leukocytes: complement activation pathway requirements in defense against Neisseria meningitidis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary properdin deficiency in three families of Tunisian Jews

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent meningococcal septicaemia and properdin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatellite

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meningococcal disease and polymorphism of FcgammaRIIa (CD32) in late complement component-deficient individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human properdin deficiency has a heterogeneous genetic background

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunochemical quantitation of antigens by single radial immunodiffusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of the alternate pathway of human complements by rabbit cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma protein measurements as a diagnostic aid.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lyonization in hemophilia: a cause of error in direct detection of heterozygous carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgG subclass levels in infancy and childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for deficiencies in the classical and alternative pathways of complement by hemolysis in gel.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of optimal reaction conditions for an assay of the human alternative complement pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properdin deficiency in a family with fulminant meningococcal infections.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The alternative pathway of complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Response to immunization with Haemophilus influenzae type b polysaccharide-pertussis vaccine and risk of Haemophilus meningitis in children with the Km(1) immunoglobulin allotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent sinopulmonary infection and impaired antibody response to bacterial capsular polysaccharide antigen in children with selective IgG-subclass deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgG subclass deficiency in adults: a clinical and immunological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bactericidal activity for Neisseria meningitidis in properdin-deficient sera

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital properdin deficiency and meningococcal infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dysfunctional properdin in a Dutch family with meningococcal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The regulation of IgG subclass production in man: low serum IgG4 in inherited deficiencies of the classical pathway of C3 activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second variant of properdin deficiency: the detection of properdin at low concentrations in affected males.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgG subclasses of pneumococcal antibodies--effect of allotype G2m(n)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Host and bacterial factors associated with Haemophilus influenzae type b disease in Minnesota children vaccinated with type b polysaccharide vaccine

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immune response to tetravalent meningococcal vaccine: opsonic and bactericidal functions of normal and properdin deficient sera

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of homozygous C4B deficiency with bacterial meningitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4B deficiency: a risk factor for bacteremia with encapsulated organisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Burkitt lymphoma and genetic markers of immunoglobulin

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited complement deficiency states: implications for immunity and immunological disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgG subclass antibodies to serogroup B meningococcal outer membrane antigens following infection and vaccination

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptibility to invasive Haemophilus influenzae type b disease and the immunoglobulin G2m(n) allotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bidirectional solid-phase sequencing of in vitro-amplified plasmid DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allotype-associated differences in concentrations of human IgG subclasses

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infectious diseases associated with complement deficiencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal human serum depleted of C1q, factor D and properdin: its use in studies of complement activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10540191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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