(Q37923353)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

review article

1 reference

title

Insights into NK cell biology from human genetics and disease associations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

author name string

Stephanie M Wood

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Hans-Gustaf Ljunggren

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

publication date

27 August 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

number of pages

15

1 reference

Cellular and Molecular Life Sciences

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

volume

68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

issue

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

page(s)

3479-3493

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

Functions of natural killer cells

11 February 2020

cites work

1 reference

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Secretory mechanisms in cell-mediated cytotoxicity

21 January 2018

1 reference

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Cytotoxic immunological synapses

21 January 2018

1 reference

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Noncytotoxic functions of NK cells: direct pathogen restriction and assistance to adaptive immunity

21 January 2018

1 reference

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Innate or adaptive immunity? The example of natural killer cells

21 January 2018

1 reference

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Severe herpesvirus infections in an adolescent without natural killer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Evolutionary struggles between NK cells and viruses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Human natural killer cell deficiencies

21 January 2018

1 reference

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Natural killer cells and cancer

21 January 2018

1 reference

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Natural killer cells in human autoimmunity

21 January 2018

1 reference

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Natural killer cells in atopic and autoimmune diseases of the skin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Human natural killer cell development

21 January 2018

1 reference

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The abundant NK cells in human secondary lymphoid tissues require activation to express killer cell Ig-like receptors and become cytolytic

21 January 2018

1 reference

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CD56brightCD16- killer Ig-like receptor- NK cells display longer telomeres and acquire features of CD56dim NK cells upon activation.

21 January 2018

1 reference

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Regulation of human NK-cell cytokine and chemokine production by target cell recognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

CD94 surface density identifies a functional intermediary between the CD56bright and CD56dim human NK-cell subsets

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

CD62L expression identifies a unique subset of polyfunctional CD56dim NK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

CD57 defines a functionally distinct population of mature NK cells in the human CD56dimCD16+ NK-cell subset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Human NK cell education by inhibitory receptors for MHC class I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

The unique properties of uterine NK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Line of attack: NK cell specificity and integration of signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Activation, coactivation, and costimulation of resting human natural killer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Formation and function of the lytic NK-cell immunological synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Minimal requirement for induction of natural cytotoxicity and intersection of activation signals by inhibitory receptors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Rapid lytic granule convergence to the MTOC in natural killer cells is dependent on dynein but not cytolytic commitment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Natural killer cell signal integration balances synapse symmetry and migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Synergistic signals for natural cytotoxicity are required to overcome inhibition by c-Cbl ubiquitin ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Integrin-dependent organization and bidirectional vesicular traffic at cytotoxic immune synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Perforin-mediated target-cell death and immune homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Degranulation plays an essential part in regulating cell surface expression of Fas ligand in T cells and natural killer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Differential secretion of Fas ligand- or APO2 ligand/TNF-related apoptosis-inducing ligand-carrying microvesicles during activation-induced death of human T cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Mechanisms and functions for the duration of intercellular contacts made by lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Natural killer cells in antiviral defense: function and regulation by innate cytokines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Human natural killer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Non-cytotoxic protection by human NK cells in mucosal secondary lymphoid tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Genetic defects affecting lymphocyte cytotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Primary immunodeficiencies: 2009 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Defective expression of the interleukin-2/interleukin-15 receptor beta subunit leads to a natural killer cell-deficient form of severe combined immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

VDUP1 is required for the development of natural killer cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Mutation of Jak3 in a patient with SCID: essential role of Jak3 in lymphoid development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

New insights into the regulation of T cells by gamma(c) family cytokines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Severe growth hormone insensitivity resulting from total absence of signal transducer and activator of transcription 5b.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Adenosine deaminase deficiency increases thymic apoptosis and causes defective T cell receptor signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Familial NK cell deficiency associated with impaired IL-2- and IL-15-dependent survival of lymphocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Development of peripheral lymphoid organs and natural killer cells depends on the helix-loop-helix inhibitor Id2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

The basic leucine zipper transcription factor E4BP4 is essential for natural killer cell development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

T-bet regulates the terminal maturation and homeostasis of NK and Valpha14i NKT cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Genetic etiologies of leukocyte adhesion defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A novel mutation in the FcgammaRIIIA gene (CD16) results in active natural killer cells lacking CD16.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

CD226 Gly307Ser association with multiple autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

The role of the activating receptor NKG2D in autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Genome-wide association study in alopecia areata implicates both innate and adaptive immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

The Yin and Yang of HLA and KIR in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Association of killer cell immunoglobulin-like receptors with scleroderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Major histocompatibility complex class I-recognizing receptors are disease risk genes in rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Homozygous human TAP peptide transporter mutation in HLA class I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Splice acceptor site mutation of the transporter associated with antigen processing-1 gene in human bare lymphocyte syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Description of HLA class I- and CD8-deficient patients: Insights into the function of cytotoxic T lymphocytes and NK cells in host defense

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

T-B+NK+ severe combined immunodeficiency caused by complete deficiency of the CD3zeta subunit of the T-cell antigen receptor complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Wiskott-Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cell-activating immunologic synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Impaired NK-cell migration in WAS/XLT patients: role of Cdc42/WASp pathway in the control of chemokine-induced beta2 integrin high-affinity state

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Requirement for caspase-8 in NF-kappaB activation by antigen receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

SLAM receptors and SAP influence lymphocyte interactions, development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

The proapoptotic function of SAP provides a clue to the clinical picture of X-linked lymphoproliferative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Differential regulation of human NK cell-mediated cytotoxicity by the tyrosine kinase Itk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

ORAI1 and STIM1 deficiency in human and mice: roles of store-operated Ca2+ entry in the immune system and beyond.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

21 January 2018

Hemophagocytic syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Temperature sensitivity of human perforin mutants unmasks subtotal loss of cytotoxicity, delayed FHL, and a predisposition to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Identification of the homologous beige and Chediak-Higashi syndrome genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Novel insights from adaptor protein 3 complex deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Mechanisms of membrane fusion: disparate players and common principles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Improvement of deficient natural killer activity and delayed bactericidal activity by a thiol proteinase inhibitor, E-64-d, in leukocytes from Chediak-Higashi syndrome patients in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Perforin: structure, function, and role in human immunopathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

The structural basis for membrane binding and pore formation by lymphocyte perforin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

In vitro- and ex vivo-derived cytolytic leukocytes from granzyme A x B double knockout mice are defective in granule-mediated apoptosis but not lysis of target cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A family with Papillon-Lefevre syndrome reveals a requirement for cathepsin C in granzyme B activation and NK cell cytolytic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Different NK cell-activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Family-wide characterization of the DENN domain Rab GDP-GTP exchange factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Munc13-4 is a GTP-Rab27-binding protein regulating dense core granule secretion in platelets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Slp1 and Slp2-a localize to the plasma membrane of CTL and contribute to secretion from the immunological synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Centrosome polarization delivers secretory granules to the immunological synapse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Distinct role of rab27a in granule movement at the plasma membrane and in the cytosol of NK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Rab27a is required for regulated secretion in cytotoxic T lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Myosin IIA associates with NK cell lytic granules to enable their interaction with F-actin and function at the immunological synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Myosin IIA is required for cytolytic granule exocytosis in human NK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Beta phorbol ester- and diacylglycerol-induced augmentation of transmitter release is mediated by Munc13s and not by PKCs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

SNAREs--engines for membrane fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Seven novel mammalian SNARE proteins localize to distinct membrane compartments

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Syntaxin 11 is an atypical SNARE abundant in the immune system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Munc18-2, a functional partner of syntaxin 3, controls apical membrane trafficking in epithelial cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Slp4-a/granuphilin-a interacts with syntaxin-2/3 in a Munc18-2-dependent manner.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Expression patterns of NKG2A, KIR, and CD57 define a process of CD56dim NK-cell differentiation uncoupled from NK-cell education

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Fatal varicella associated with selective natural killer cell deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Primary immunodeficiencies: increasing market share

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Innate immunity defects in Hermansky-Pudlak type 2 syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Calmodulin and Munc13 Form a Ca2+ Sensor/Effector Complex that Controls Short-Term Synaptic Plasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

A new immunodeficiency disorder in humans involving NK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0799-Y

Defective neutrophil and lymphocyte function in leucocyte adhesion deficiency

21 January 2018

1 reference

12 December 2020

Expression of recombinant human granzyme B. A processing and activation role for dipeptidyl peptidase I.

1 reference

12 December 2020

Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcgammaRIIIa gene

1 reference

12 December 2020

The loss of the CD16 B73.1/Leu11c epitope occurring in some primary immunodeficiency diseases is not associated with the FcgammaRIIIa-48L/R/H polymorphism

1 reference

12 December 2020

ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis

1 reference

12 December 2020

Characterization of immunodeficiency in a patient with growth hormone insensitivity secondary to a novel STAT5b gene mutation

1 reference

12 December 2020

Syntaxin 11 is associated with SNAP-23 on late endosomes and the trans-Golgi network

1 reference

12 December 2020

The genetic deficiency of leukocyte surface glycoprotein Mac-1, LFA-1, p150,95 in humans is associated with defective antibody-dependent cellular cytotoxicity in vitro and defective protection against herpes simplex virus infection in vivo

1 reference

12 December 2020

The 158V polymorphism of Fc gamma receptor type IIIA in early rheumatoid arthritis: increased susceptibility and severity in male patients (the Swedish TIRA project)

1 reference

12 December 2020

Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms

1 reference

12 December 2020

Modelling KIR-HLA genotype disparities in type 1 diabetes

1 reference

12 December 2020

Functional characterization of natural killer cells in type I leukocyte adhesion deficiency

1 reference

12 December 2020

Cutting edge: heterozygote advantage in autoimmune disease: hierarchy of protection/susceptibility conferred by HLA and killer Ig-like receptor combinations in psoriatic arthritis

1 reference

12 December 2020

Loss of cytotoxic T lymphocyte function in Chediak-Higashi syndrome arises from a secretory defect that prevents lytic granule exocytosis

1 reference

12 December 2020

IL-15 receptor maintains lymphoid homeostasis by supporting lymphocyte homing and proliferation

1 reference

12 December 2020

Restimulation-induced apoptosis of T cells is impaired in patients with X-linked lymphoproliferative disease caused by SAP deficiency.

1 reference

12 December 2020

Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity

1 reference

12 December 2020

Deficient Natural Killer Cell Activity in X-Linked Lymphoproliferative Syndrome

1 reference

12 December 2020

Growth hormone insensitivity associated with a STAT5b mutation

1 reference

12 December 2020

Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II

1 reference

12 December 2020

10.1007/S00018-011-0799-Y

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21874350%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference