Impaired respiratory burst contributes to infections in PKCδ-deficient patients
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Title
Impaired respiratory burst contributes to infections in PKCδ-deficient patients
Authors
Keywords
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Journal
JOURNAL OF EXPERIMENTAL MEDICINE
Volume 218, Issue 9, Pages -
Publisher
Rockefeller University Press
Online
2021-07-15
DOI
10.1084/jem.20210501
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Note: Only part of the references are listed.- Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature
- (2020) Niusha Sharifinejad et al. IMMUNOLOGICAL INVESTIGATIONS
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- (2020) Isabelle Meyts et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- The Role of Tyrosine Phosphorylation of Protein Kinase C Delta in Infection and Inflammation
- (2019) Qingliang Yang et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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- (2019) Mathew Wright et al. JOURNAL OF PEDIATRICS
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- (2019) Ommar Omarjee et al. AUTOIMMUNITY REVIEWS
- Origin and ontogeny of lung macrophages: from mice to humans
- (2019) Elza Evren et al. IMMUNOLOGY
- NADPH oxidase activation in neutrophils: Role of the phosphorylation of its subunits
- (2018) Sahra A. Belambri et al. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
- Impaired IFN γ -Signaling and Mycobacterial Clearance in IFN γ R1-Deficient Human iPSC-Derived Macrophages
- (2018) Anna-Lena Neehus et al. Stem Cell Reports
- Inherited p40phox deficiency differs from classic chronic granulomatous disease
- (2018) Annemarie van de Geer et al. JOURNAL OF CLINICAL INVESTIGATION
- Successful use of ofatumumab in two cases of early-onset juvenile SLE with thrombocytopenia caused by a mutation in protein kinase C δ
- (2018) Linda Lei et al. Pediatric Rheumatology
- Protein Kinase C-Delta (PKCδ) Tyrosine Phosphorylation is a Critical Regulator of Neutrophil-Endothelial Cell Interaction in Inflammation
- (2018) Fariborz Soroush et al. SHOCK
- EROS/CYBC1 mutations: Decreased NADPH oxidase function and chronic granulomatous disease
- (2018) David C. Thomas et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Modelling IRF8 Deficient Human Hematopoiesis and Dendritic Cell Development with Engineered iPS Cells
- (2017) Stephanie Sontag et al. STEM CELLS
- Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
- (2016) Francesca Conti et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Protein Kinase C δ: a Gatekeeper of Immune Homeostasis
- (2016) Elisabeth Salzer et al. JOURNAL OF CLINICAL IMMUNOLOGY
- PKC-δ activation in neutrophils promotes fungal clearance
- (2016) Xun Li et al. JOURNAL OF LEUKOCYTE BIOLOGY
- Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease
- (2016) Christian Lood et al. NATURE MEDICINE
- Association Between Discoid Lupus Erythematosus and Chronic Granulomatous Disease-Report of Two Cases and Review of the Literature
- (2016) Charles Xie et al. PEDIATRIC DERMATOLOGY
- Early-Onset Juvenile SLE Associated With a Novel Mutation in Protein Kinase C δ
- (2016) Sira Nanthapisal et al. PEDIATRICS
- Impaired microbial killing by neutrophils from patients with protein kinase C delta deficiency
- (2015) Katka Szilagyi et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency
- (2015) Francesca Conti et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency
- (2015) Ayca Kiykim et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry
- (2015) Edgar Borges de Oliveira-Junior et al. PEDIATRIC BLOOD & CANCER
- Large-Scale Hematopoietic Differentiation of Human Induced Pluripotent Stem Cells Provides Granulocytes or Macrophages for Cell Replacement Therapies
- (2015) Nico Lachmann et al. Stem Cell Reports
- Common Severe Infections in Chronic Granulomatous Disease
- (2014) B. E. Marciano et al. CLINICAL INFECTIOUS DISEASES
- Molecular Insights of p47phoxPhosphorylation Dynamics in the Regulation of NADPH Oxidase Activation and Superoxide Production
- (2014) Daniel N. Meijles et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Protein Kinase C Promotes Transitional B Cell-Negative Selection and Limits Proximal B Cell Receptor Signaling To Enforce Tolerance
- (2014) A. Limnander et al. MOLECULAR AND CELLULAR BIOLOGY
- Chronic granulomatous disease associated with systemic lupus erythematosus and systemic onset juvenile idiopathic arthritis
- (2014) Vadood Parvaneh et al. Pediatric Rheumatology
- Protein Kinase Cδ Deficiency Causes Mendelian Systemic Lupus Erythematosus With B Cell-Defective Apoptosis and Hyperproliferation
- (2013) Alexandre Belot et al. ARTHRITIS AND RHEUMATISM
- B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C
- (2013) E. Salzer et al. BLOOD
- Loss-of-function of the protein kinase C (PKC ) causes a B-cell lymphoproliferative syndrome in humans
- (2013) H. S. Kuehn et al. BLOOD
- Isozyme-specific Interaction of Protein Kinase Cδ with Mitochondria Dissected Using Live Cell Fluorescence Imaging
- (2012) Alyssa X. Wu-Zhang et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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- (2012) Sayna Norouzi et al. JOURNAL OF INFECTION
- Type I interferonopathies: a novel set of inborn errors of immunity
- (2011) Yanick J. Crow Annals of the New York Academy of Sciences
- PKC-delta and PKC-epsilon: Foes of the same family or strangers?
- (2011) Nicolas Duquesnes et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease
- (2011) Jacinta Bustamante et al. NATURE IMMUNOLOGY
- STIM1, PKC-δ and RasGRP set a threshold for proapoptotic Erk signaling during B cell development
- (2011) Andre Limnander et al. NATURE IMMUNOLOGY
- Two Faces of Protein Kinase Cδ: The Contrasting Roles of PKCδ in Cell Survival and Cell Death
- (2011) Alakananda Basu et al. TheScientificWorldJOURNAL
- Phosphorylation of threonine 154 in p40phox is an important physiological signal for activation of the neutrophil NADPH oxidase
- (2010) T. A. M. Chessa et al. BLOOD
- A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity
- (2009) J. D. Matute et al. BLOOD
- p47phox, the phagocyte NADPH oxidase/NOX2 organizer: structure, phosphorylation and implication in diseases
- (2009) Jamel El-Benna et al. EXPERIMENTAL AND MOLECULAR MEDICINE
- B-cell tolerance checkpoints in health and autoimmunity
- (2008) Eric Meffre et al. CURRENT OPINION IN IMMUNOLOGY
- Systemic Lupus Erythematosus
- (2008) Anisur Rahman et al. NEW ENGLAND JOURNAL OF MEDICINE
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