(Q38102968)

28 August 2017

title

Defects of leukocyte migration in primary immunodeficiencies (English)

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28 August 2017

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1

Raffaele Badolato

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28 August 2017

language of work or name

English

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publication date

1 June 2013

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European Journal of Immunology

28 August 2017

published in

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28 August 2017

volume

43

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28 August 2017

issue

6

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28 August 2017

page(s)

1436-1440

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Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease

28 August 2017

cites work

1 reference

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Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome

21 January 2018

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Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome

21 January 2018

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Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry

21 January 2018

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WHIM syndrome caused by a single amino acid substitution in the carboxy-tail of chemokine receptor CXCR4.

21 January 2018

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Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients.

21 January 2018

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WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus-truncated CXCR4

21 January 2018

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Tetralogy of fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome

21 January 2018

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Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development

21 January 2018

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Disrupted cardiac development but normal hematopoiesis in mice deficient in the second CXCL12/SDF-1 receptor, CXCR7

21 January 2018

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Enhanced function with decreased internalization of carboxy-terminus truncated CXCR4 responsible for WHIM syndrome

21 January 2018

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Live imaging of neutrophil motility in a zebrafish model of WHIM syndrome

21 January 2018

1 reference

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The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome

21 January 2018

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Oligoclonality, impaired class switch and B-cell memory responses in WHIM syndrome

21 January 2018

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The CXCR4 antagonist plerixafor is a potential therapy for myelokathexis, WHIM syndrome

21 January 2018

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WASP: a key immunological multitasker

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

WASP-interacting protein (WIP): working in polymerisation and much more

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

Mutations of the Wiskott-Aldrich Syndrome Protein affect protein expression and dictate the clinical phenotypes

21 January 2018

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Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Chemotaxis of macrophages is abolished in the Wiskott-Aldrich syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Configuration of human dendritic cell cytoskeleton by Rho GTPases, the WAS protein, and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

The chemotactic defect in wiskott-Aldrich syndrome macrophages is due to the reduced persistence of directional protrusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Reduced type I interferon production by dendritic cells and weakened antiviral immunity in patients with Wiskott-Aldrich syndrome protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

WASP deficiency leads to global defects of directed leukocyte migration in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Neutrophil-active chemokines in in vivo imaging of neutrophil trafficking.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Cdc42 regulates neutrophil migration via crosstalk between WASp, CD11b, and microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

The interaction between Cdc42 and WASP is required for SDF-1-induced T-lymphocyte chemotaxis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

WASP confers selective advantage for specific hematopoietic cell populations and serves a unique role in marginal zone B-cell homeostasis and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

B cell-intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice.

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

Wiskott-Aldrich syndrome protein (WASP) and N-WASP are critical for peripheral B-cell development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

A defect in hematopoietic stem cell migration explains the nonrandom X-chromosome inactivation in carriers of Wiskott-Aldrich syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Hematologically important mutations: leukocyte adhesion deficiency (first update).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Leukocyte adhesion deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Structural basis of integrin regulation and signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Allogeneic hematopoietic stem-cell transplantation for leukocyte adhesion deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Insights into leukocyte adhesion deficiency type 2 from a novel mutation in the GDP-fucose transporter gene.

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

Leukocyte adhesion deficiency II patients with a dual defect of the GDP-fucose transporter

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

Leukocyte adhesion deficiency type II: long-term follow-up and review of the literature

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

LAD III versus LAD I variant

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

LAD-1/variant syndrome is caused by mutations in FERMT3.

21 January 2018

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https://api.crossref.org/works/10.1002%2FEJI.201243155

Kindlin-3: a new gene involved in the pathogenesis of LAD-III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Kindlin-3-mediated signaling from multiple integrin classes is required for osteoclast-mediated bone resorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Proper desensitization of CXCR4 is required for lymphocyte development and peripheral compartmentalization in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

Regulation of human chemokine receptors CXCR4. Role of phosphorylation in desensitization and internalization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

An unusual form of chronic neutropenia in a father and daughter with hypogammaglobulinaemia

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

Impaired T-cell priming in vivo resulting from dysfunction of WASp-deficient dendritic cells

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

Cytoskeletal remodeling mediated by WASp in dendritic cells is necessary for normal immune synapse formation and T-cell priming

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

An inherited abnormality of neutrophil adhesion. Its genetic transmission and its association with a missing protein

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

The clinical spectrum of leukocyte adhesion deficiency (LAD) III due to defective CalDAG-GEF1

1 reference

https://api.crossref.org/works/10.1002%2FEJI.201243155

7 January 2021

Identifiers

DOI

10.1002/EJI.201243155

1 reference

28 August 2017

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