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English
Antibody deficiency diseases.
scientific article published on February 2008
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Antibody deficiency diseases
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
main subject
antibody
1 reference
based on heuristic
inferred from title
author
Qiang Pan-Hammarström
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
Lennart Hammarström
series ordinal
2
object named as
Lennart Hammarström
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
language of work or name
English
0 references
publication date
1 February 2008
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
published in
European Journal of Immunology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
volume
38
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
page(s)
327-333
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
cites work
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunological and genetic bases of new primary immunodeficiencies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pyogenic bacterial infections in humans with IRAK-4 deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Herpes simplex virus encephalitis in human UNC-93B deficiency
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TLR3 deficiency in patients with herpes simplex encephalitis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary immunodeficiencies: a field in its infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BCG-osis and tuberculosis in a child with chronic granulomatous disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
STAT3 mutations in the hyper-IgE syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Omenn syndrome in an infant with IL7RA gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic analysis of patients with defects in early B-cell development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and molecular analysis of patients with defects in micro heavy chain gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new case of autosomal recessive agammaglobulinaemia with impaired pre-B cell differentiation due to a large deletion of the IGH locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of IgA in C(mu)-deficient patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in Igalpha (CD79a) result in a complete block in B-cell development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the Igbeta gene cause agammaglobulinemia in man.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TACI is mutant in common variable immunodeficiency and IgA deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant-negative effect of the heterozygous C104R TACI mutation in common variable immunodeficiency (CVID)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An antibody-deficiency syndrome due to mutations in the CD19 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deconstructing common variable immunodeficiency by genetic analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role for Msh5 in the regulation of Ig class switch recombination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunodeficiencies with autoimmune consequences.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational analysis of human BLyS in patients with common variable immunodeficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational Analysis of Human BAFF Receptor TNFRSF13C (BAFF-R) in Patients with Common Variable Immunodeficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Does 77C-->G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired IgA class switching in APRIL-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unusual case presentations associated with the CD45 C77G polymorphism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Correction of prototypic ATM splicing mutations and aberrant ATM function with antisense morpholino oligonucleotides
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FEJI.200737927
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/EJI.200737927
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
PubMed publication ID
18200502
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18200502
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18200502%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
ResearchGate publication ID
5650057
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