(Q39396357)

11 September 2017

Novel mutation in STXBP2 prevents IL-2-induced natural killer cell cytotoxicity (English)

1 reference

11 September 2017

0 references

Rushani W Saltzman

1

1 reference

11 September 2017

Linda Monaco-Shawver

2

1 reference

11 September 2017

Kejian Zhang

3

1 reference

11 September 2017

Kathleen E Sullivan

4

1 reference

11 September 2017

Alexandra H Filipovich

5

1 reference

11 September 2017

Jordan S Orange

6

1 reference

11 September 2017

language of work or name

English

0 references

publication date

14 February 2012

1 reference

The Journal of Allergy and Clinical Immunology

11 September 2017

1 reference

11 September 2017

129

1 reference

11 September 2017

6

1 reference

11 September 2017

1666-1668

1 reference

IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

Formation and function of the lytic NK-cell immunological synapse

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3646578

10.1016/J.JACI.2011.12.1003

14 September 2017

Identifiers

DOI

1 reference

11 September 2017

1 reference

11 September 2017

PubMed publication ID

22336081

1 reference