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Novel mutations in a Japanese patient with CD19 deficiency
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1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
title
Novel mutations in a Japanese patient with CD19 deficiency
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
main subject
immunology
0 references
author
Mostafa Mohamed Sira
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Menno C van Zelm
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
author name string
H Kanegane
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
K Agematsu
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
T Futatani
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
K Suga
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
T Sekiguchi
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
T Miyawaki
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
publication date
20 September 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
published in
Genes and Immunity
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
volume
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
page(s)
663-670
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
cites work
Primary immunodeficiency diseases. Report of an IUIS Scientific Committee. International Union of Immunological Societies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
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/10.1038%2FSJ.GENE.6364431
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/10.1038%2FSJ.GENE.6364431
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/10.1038%2FSJ.GENE.6364431
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/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CD19: lowering the threshold for antigen receptor stimulation of B lymphocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dual antigen recognition by B cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of memory B cells in patients with common variable immunodeficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A solid-phase enzyme-linked immunospot (ELISPOT) assay for enumeration of specific antibody-secreting cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human dendritic cells skew isotype switching of CD40-activated naive B cells towards IgA1 and IgA2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/SJ.GENE.6364431
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Dimensions Publication ID
1049139451
0 references
PubMed publication ID
17882224
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17882224
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
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