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The who, where, and when of IgE in allergic airway disease

Journal of allergy and clinical immunology, 2012-03, Vol.129 (3), p.635-645

2012

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Structural Activation of Pro-inflammatory Human Cytokine IL-23 by Cognate IL-23 Receptor Enables Recruitment of the Shared Receptor IL-12Rβ1

Immunity (Cambridge, Mass.), 2018-01, Vol.48 (1), p.45-58.e6

2018

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Treatment of intestinal fibrosis in experimental inflammatory bowel disease by the pleiotropic actions of a local Rho kinase inhibitor

Gastroenterology (New York, N.Y. 1943), 2017-10, Vol.153 (4), p.1054-1067

2017

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Familial Mediterranean fever mutations lift the obligatory requirement for microtubules in Pyrin inflammasome activation

Proceedings of the National Academy of Sciences - PNAS, 2016-12, Vol.113 (50), p.14384-14389

2016

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House dust mite–driven asthma and allergen-specific T cells depend on B cells when the amount of inhaled allergen is limiting

Journal of allergy and clinical immunology, 2017-07, Vol.140 (1), p.76-88.e7

2017

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Ikaros family zinc finger 1 regulates dendritic cell development and function in humans

Nature communications, 2018-03, Vol.9 (1), p.1239-10, Article 1239

2018

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Local immunoglobulin e in the nasal mucosa: clinical implications

Allergy, 2015, Asthma & Immunology Research, 7(4), , pp.321-331

2015

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A Computational Pipeline for the Diagnosis of CVID Patients

Frontiers in immunology, 2019-08, Vol.10, p.2009-2009

2019

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Reliable mite-specific IgE testing in nasal secretions by means of allergen microarray

Journal of allergy and clinical immunology, 2017-07, Vol.140 (1), p.301-303.e8

2017

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Macrophages induce differentiation of plasma cells through CXCL10/IP-10

The Journal of experimental medicine, 2012-09, Vol.209 (10), p.1813-1823

2012

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Haematopoietic prolyl hydroxylase‐1 deficiency promotes M2 macrophage polarization and is both necessary and sufficient to protect against experimental colitis

The Journal of pathology, 2017-03, Vol.241 (4), p.547-558

2017

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A CARD9 Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation

Frontiers in immunology, 2018-10, Vol.9, p.2366-2366

2018

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Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

Scientific reports, 2017-06, Vol.7 (1), p.3702-12, Article 3702

2017

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Motivations, barriers and experiences of participants in an HIV reservoir trial

Journal of Virus Eradication, 2021-03, Vol.7 (1), p.100029-100029, Article 100029

2021

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Persistent rotavirus diarrhea post-transplant in a novel JAK3-SCID patient after vaccination

Pediatric allergy and immunology, 2016-02, Vol.27 (1), p.93-96

2016

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The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives

Haematologica (Roma), 2017-01, Vol.102 (1), p.192

2017

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Brucella β 1,2 cyclic glucan is an activator of human and mouse dendritic cells

PLoS pathogens, 2012-11, Vol.8 (11), p.e1002983-e1002983

2012

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Local inflammation in chronic upper airway disease

Current pharmaceutical design, 2012-06, Vol.18 (16), p.2336

2012

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From pathogen to medicine: HIV-1-derived lentiviral vectors as vehicles for dendritic cell based cancer immunotherapy

The journal of gene medicine, 2006-01, Vol.8 (1), p.3-17

2006

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When One Rare Disease Hides Another: Kartagener Syndrome Masking FMF

Clinical pediatrics, 2018-07, Vol.57 (8), p.981-985

2018

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Lentivirally transduced dendritic cells as a tool for cancer immunotherapy

The journal of gene medicine, 2003-08, Vol.5 (8), p.654-667

2003

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Genes associated with common variable immunodeficiency: one diagnosis to rule them all?

Journal of Medical Genetics, 2016-09, Vol.53 (9), p.575-590

2016

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Human Blood CXCR5+CD4+ T Cells Are Counterparts of T Follicular Cells and Contain Specific Subsets that Differentially Support Antibody Secretion

Immunity (Cambridge, Mass.), 2011-01, Vol.34 (1), p.108-121

2011

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Efficient genetic modification of murine dendritic cells by electroporation with mRNA

Cancer gene therapy, 2002-09, Vol.9 (9), p.787-797

2002

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The who, where, and when of IgE in allergic airway disease

Structural Activation of Pro-inflammatory Human Cytokine IL-23 by Cognate IL-23 Receptor Enables Recruitment of the Shared Receptor IL-12Rβ1

Treatment of intestinal fibrosis in experimental inflammatory bowel disease by the pleiotropic actions of a local Rho kinase inhibitor

Familial Mediterranean fever mutations lift the obligatory requirement for microtubules in Pyrin inflammasome activation

House dust mite–driven asthma and allergen-specific T cells depend on B cells when the amount of inhaled allergen is limiting

Ikaros family zinc finger 1 regulates dendritic cell development and function in humans

Local immunoglobulin e in the nasal mucosa: clinical implications

A Computational Pipeline for the Diagnosis of CVID Patients

Reliable mite-specific IgE testing in nasal secretions by means of allergen microarray

Macrophages induce differentiation of plasma cells through CXCL10/IP-10

Haematopoietic prolyl hydroxylase‐1 deficiency promotes M2 macrophage polarization and is both necessary and sufficient to protect against experimental colitis

A CARD9 Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation

Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

Motivations, barriers and experiences of participants in an HIV reservoir trial

Persistent rotavirus diarrhea post-transplant in a novel JAK3-SCID patient after vaccination

The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives

Brucella β 1,2 cyclic glucan is an activator of human and mouse dendritic cells

Local inflammation in chronic upper airway disease

From pathogen to medicine: HIV-1-derived lentiviral vectors as vehicles for dendritic cell based cancer immunotherapy

When One Rare Disease Hides Another: Kartagener Syndrome Masking FMF

Lentivirally transduced dendritic cells as a tool for cancer immunotherapy

Genes associated with common variable immunodeficiency: one diagnosis to rule them all?

Human Blood CXCR5+CD4+ T Cells Are Counterparts of T Follicular Cells and Contain Specific Subsets that Differentially Support Antibody Secretion

Efficient genetic modification of murine dendritic cells by electroporation with mRNA

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

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