(Q63804793)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Novel mutations in a Japanese patient with CD19 deficiency (English)

1 reference

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7 January 2020

0 references

4

1 reference

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7 January 2020

Menno C van Zelm

7

1 reference

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7 January 2020

author name string

H Kanegane

1

1 reference

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7 January 2020

K Agematsu

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

T Futatani

3

1 reference

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7 January 2020

K Suga

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

T Sekiguchi

6

1 reference

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7 January 2020

T Miyawaki

8

1 reference

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7 January 2020

publication date

20 September 2007

1 reference

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7 January 2020

1 reference

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7 January 2020

volume

8

1 reference

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7 January 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17882224%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

663-670

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.gene.6364431

7 January 2020

exact match

0 references

cites work

Primary immunodeficiency diseases. Report of an IUIS Scientific Committee. International Union of Immunological Societies

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7 January 2021

Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry

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7 January 2021

Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?

1 reference

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7 January 2021

Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

1 reference

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7 January 2021

An antibody-deficiency syndrome due to mutations in the CD19 gene

1 reference

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7 January 2021

CD19: lowering the threshold for antigen receptor stimulation of B lymphocytes

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7 January 2021

Dual antigen recognition by B cells

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7 January 2021

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

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7 January 2021

Absence of memory B cells in patients with common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

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

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

A solid-phase enzyme-linked immunospot (ELISPOT) assay for enumeration of specific antibody-secreting cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021

Human dendritic cells skew isotype switching of CD40-activated naive B cells towards IgA1 and IgA2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364431

7 January 2021