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Title
Human hyper-IgE syndrome: singular or plural?
Authors
Keywords
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Journal
MAMMALIAN GENOME
Volume 29, Issue 7-8, Pages 603-617
Publisher
Springer Nature America, Inc
Online
2018-08-09
DOI
10.1007/s00335-018-9767-2
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- (2017) Romain Péanne et al. European Journal of Medical Genetics
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- (2017) Anne Kosfeld et al. HUMAN MOLECULAR GENETICS
- IgE sensitization in relation to preschool eczema and filaggrin mutation
- (2017) Emma Kristin Johansson et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Dedicator of cytokinesis 8–deficient CD4 + T cells are biased to a T H 2 effector fate at the expense of T H 1 and T H 17 cells
- (2017) Stuart G. Tangye et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
- (2017) Capucine Picard et al. JOURNAL OF CLINICAL IMMUNOLOGY
- A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis
- (2017) Tobias Schwerd et al. JOURNAL OF EXPERIMENTAL MEDICINE
- DOCK8 Drives Src-Dependent NK Cell Effector Function
- (2017) Conor J. Kearney et al. JOURNAL OF IMMUNOLOGY
- A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients
- (2017) Leila Ben-Khemis et al. MOLECULAR IMMUNOLOGY
- Germline hypomorphic CARD11 mutations in severe atopic disease
- (2017) Chi A Ma et al. NATURE GENETICS
- IgG1 memory B cells keep the memory of IgE responses
- (2017) Jin-Shu He et al. Nature Communications
- DOCK8: regulator of Treg in response to corticotropin-releasing hormone
- (2016) S. Jin et al. ALLERGY
- Genetic defects in the hexosamine and sialic acid biosynthesis pathway
- (2016) Anke P. Willems et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- A viable mouse model for Netherton syndrome based on mosaic inactivation of the Spink5 gene
- (2016) Petr Kasparek et al. BIOLOGICAL CHEMISTRY
- STAT3 signaling in immunity
- (2016) Emily J. Hillmer et al. CYTOKINE & GROWTH FACTOR REVIEWS
- Tyrosine kinase 2 is not limiting human antiviral type III interferon responses
- (2016) Sebastian Fuchs et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Fifty years later: Emerging functions of IgE antibodies in host defense, immune regulation, and allergic diseases
- (2016) Hans C. Oettgen JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- B-cell–specific STAT3 deficiency: Insight into the molecular basis of autosomal-dominant hyper-IgE syndrome
- (2016) Alisa Kane et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Neonatal-onset T − B − NK + severe combined immunodeficiency and neutropenia caused by mutated phosphoglucomutase 3
- (2016) Jens Magnus Bernth-Jensen et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Identification of IgE
- (2016) Kimishige Ishizaka et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Human B-cell isotype switching origins of IgE
- (2016) Timothy J. Looney et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes T H 17 cell differentiation
- (2016) Sevgi Keles et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Recent Advances in DOCK8 Immunodeficiency Syndrome
- (2016) Qian Zhang et al. JOURNAL OF CLINICAL IMMUNOLOGY
- A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton
- (2016) Erin Janssen et al. JOURNAL OF CLINICAL INVESTIGATION
- LRCH1 interferes with DOCK8-Cdc42–induced T cell migration and ameliorates experimental autoimmune encephalomyelitis
- (2016) Xiaoyan Xu et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+T cells into distinct effector subsets
- (2016) Cindy S. Ma et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Diagnostic value of exome and whole genome sequencing in craniosynostosis
- (2016) Kerry A Miller et al. JOURNAL OF MEDICAL GENETICS
- Netherton Syndrome: A Genotype-Phenotype Review
- (2016) Constantina A. Sarri et al. Molecular Diagnosis & Therapy
- Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency
- (2016) Romain Lévy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The JAK-STAT Pathway: Impact on Human Disease and Therapeutic Intervention
- (2015) John J. O'Shea et al. Annual Review of Medicine
- Susceptibility to infections, without concomitant hyper-IgE, reported in 1976, is caused by hypomorphic mutation in the phosphoglucomutase 3 ( PGM3 ) gene
- (2015) Karin E. Lundin et al. CLINICAL IMMUNOLOGY
- Recent advances in congenital ichthyoses
- (2015) Angela Hernández-Martín et al. CURRENT OPINION IN PEDIATRICS
- Glycoproteomic studies of IgE from a novel hyper IgE syndrome linked to PGM3 mutation
- (2015) Gang Wu et al. GLYCOCONJUGATE JOURNAL
- Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R
- (2015) B. Erman et al. HAEMATOLOGICA
- Delayed control of herpes simplex virus infection and impaired CD4+ T-cell migration to the skin in mouse models of DOCK8 deficiency
- (2015) Inge E A Flesch et al. IMMUNOLOGY AND CELL BIOLOGY
- The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
- (2015) Karin R. Engelhardt et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- The Ying and Yang of STAT3 in Human Disease
- (2015) Tiphanie P. Vogel et al. JOURNAL OF CLINICAL IMMUNOLOGY
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- (2014) Liat Samuelov et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
- (2014) Yu Zhang et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
- (2014) Atfa Sassi et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- DOCK8 regulates lymphocyte shape integrity for skin antiviral immunity
- (2014) Qian Zhang et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Mechanisms of Jak/STAT Signaling in Immunity and Disease
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- DOCK8 regulates protective immunity by controlling the function and survival of RORγt+ ILCs
- (2014) Akhilesh K. Singh et al. Nature Communications
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- (2013) G. Crawford et al. BLOOD
- Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency
- (2013) Monia Ouederni et al. CLINICAL INFECTIOUS DISEASES
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- (2013) Alexandra F. Freeman et al. DISEASE MARKERS
- An ACT1 Mutation Selectively Abolishes Interleukin-17 Responses in Humans with Chronic Mucocutaneous Candidiasis
- (2013) Bertrand Boisson et al. IMMUNITY
- Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism
- (2013) Amy P. Hsu et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency
- (2013) Melissa C. Mizesko et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation
- (2013) Andrea M. Siegel et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
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- (2013) Daniel Kotlarz et al. JOURNAL OF EXPERIMENTAL MEDICINE
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- (2013) Elissa K. Deenick et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Dedicator of Cytokinesis 8 Interacts with Talin and Wiskott-Aldrich Syndrome Protein To Regulate NK Cell Cytotoxicity
- (2013) H. Ham et al. JOURNAL OF IMMUNOLOGY
- The MEK-ERK Pathway Is Necessary for Serine Phosphorylation of Mitochondrial STAT3 and Ras-Mediated Transformation
- (2013) Daniel J. Gough et al. PLoS One
- Mutations in the interleukin receptorIL11RAcause autosomal recessive Crouzon-like craniosynostosis
- (2013) Katharina Keupp et al. Molecular Genetics & Genomic Medicine
- DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses
- (2012) Y. Harada et al. BLOOD
- Inborn errors of human IL-17 immunity underlie chronic mucocutaneous candidiasis
- (2012) Anne Puel et al. Current Opinion in Allergy and Clinical Immunology
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- (2012) Sophie Cypowyj et al. EUROPEAN JOURNAL OF IMMUNOLOGY
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- (2012) Benedikt D. Spielberger et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
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- (2012) Umaimainthan Palendira et al. JOURNAL OF EXPERIMENTAL MEDICINE
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- (2012) Huizhong Xiong et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome
- (2012) Marie-Olivia Chandesris et al. MEDICINE
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- (2012) Haifa H Jabara et al. NATURE IMMUNOLOGY
- Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth
- (2011) Pekka Nieminen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- T-regulatory cells in primary immune deficiencies
- (2011) James W. Verbsky et al. Current Opinion in Allergy and Clinical Immunology
- Hyperimmunoglobulin E syndromes in pediatrics
- (2011) Qian Zhang et al. CURRENT OPINION IN PEDIATRICS
- DOCK8 is essential for T-cell survival and the maintenance of CD8+ T-cell memory
- (2011) Teresa Lambe et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
- (2011) Katrina L. Randall et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Gain-of-function humanSTAT1mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
- (2011) Luyan Liu et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Chronic Mucocutaneous Candidiasis in Humans with Inborn Errors of Interleukin-17 Immunity
- (2011) A. Puel et al. SCIENCE
- STAT3 controls the neutrophil migratory response to CXCR2 ligands by direct activation of G-CSF-induced CXCR2 expression and via modulation of CXCR2 signal transduction
- (2010) H. Nguyen-Jackson et al. BLOOD
- STAT3 controls myeloid progenitor growth during emergency granulopoiesis
- (2010) H. Zhang et al. BLOOD
- Somatic mosaicism in the Wiskott–Aldrich syndrome: Molecular and functional characterization of genotypic revertants
- (2010) Brian R. Davis et al. CLINICAL IMMUNOLOGY
- Inborn errors of mucocutaneous immunity to Candida albicans in humans: a role for IL-17 cytokines?
- (2010) Anne Puel et al. CURRENT OPINION IN IMMUNOLOGY
- PD-L1 expression on tolerogenic APCs is controlled by STAT-3
- (2010) Sabine J. Wölfle et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Revertant T lymphocytes in a patient with Wiskott-Aldrich syndrome: Analysis of function and distribution in lymphoid organs
- (2010) Sara Trifari et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
- (2010) Cristina Woellner et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- B cell–intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans
- (2010) Danielle T. Avery et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
- (2010) Anne Puel et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Dendritic Cell (DC)-Specific Targeting Reveals Stat3 as a Negative Regulator of DC Function
- (2010) Jessica A. Melillo et al. JOURNAL OF IMMUNOLOGY
- Rapid Molecular Analysis of the STAT3 Gene in Job Syndrome of Hyper-IgE and Recurrent Infectious Diseases
- (2010) Attila Kumánovics et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Pathogenesis of Hyper IgE Syndrome
- (2009) Jennifer Heimall et al. CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
- Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
- (2009) Karin R. Engelhardt et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome
- (2009) Yoshiyuki Minegishi et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production
- (2009) Katrina L Randall et al. NATURE IMMUNOLOGY
- Combined Immunodeficiency Associated withDOCK8Mutations
- (2009) Qian Zhang et al. NEW ENGLAND JOURNAL OF MEDICINE
- Mitochondrial STAT3 Supports Ras-Dependent Oncogenic Transformation
- (2009) D. J. Gough et al. SCIENCE
- Function of Mitochondrial Stat3 in Cellular Respiration
- (2009) J. Wegrzyn et al. SCIENCE
- Long‐term follow‐up in Stuve–Wiedemann syndrome: A clinical report
- (2008) Isabel Mendes Gaspar et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Environmental determinants of total IgE among school children living in the rural Tropics: importance of geohelminth infections and effect of anthelmintic treatment
- (2008) Philip J Cooper et al. BMC IMMUNOLOGY
- Roles of unphosphorylated STATs in signaling
- (2008) Jinbo Yang et al. CELL RESEARCH
- Somatic mosaicism in primary immune deficiencies
- (2008) Taizo Wada et al. Current Opinion in Allergy and Clinical Immunology
- Hyper IgE syndrome: an update on clinical aspects and the role of signal transducer and activator of transcription 3
- (2008) Michelle L Paulson et al. Current Opinion in Allergy and Clinical Immunology
- Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome
- (2008) Ellen D. Renner et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Deficiency of Th17 cells in hyper IgE syndrome due to mutations inSTAT3
- (2008) Cindy S. Ma et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Mutations inSTAT3andIL12RB1impair the development of human IL-17–producing T cells
- (2008) Ludovic de Beaucoudrey et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein
- (2008) Pingyan Cheng et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Filaggrin null mutations are associated with atopic dermatitis and elevated levels of IgE in the Japanese population: a family and case–control study
- (2008) Hisako Enomoto et al. JOURNAL OF HUMAN GENETICS
- Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
- (2008) Joshua D. Milner et al. NATURE
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