Chronic Granulomatous Disease-Like Presentation of a Child with Autosomal Recessive PKCδ Deficiency

Impaired respiratory burst contributes to infections in PKCδ-deficient patients

(2021) Anna-Lena Neehus et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Mendelian susceptibility to mycobacterial disease: recent discoveries

(2020) Jacinta Bustamante   HUMAN GENETICS

Inherited human IFN-γ deficiency underlies mycobacterial disease

(2020) Gaspard Kerner et al.   JOURNAL OF CLINICAL INVESTIGATION

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

Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

(2020) Isabelle Meyts et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Mendelian susceptibility to mycobacterial disease: 2014-2018 update

(2018) Jérémie Rosain et al.   IMMUNOLOGY AND CELL BIOLOGY

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), a marker of inflammation and tuberculosis disease progression in humans, is important for optimal macrophage killing effector functions and survival in mice

(2017) S P Parihar et al.   Mucosal Immunology

Protein Kinase C δ: a Gatekeeper of Immune Homeostasis

(2016) Elisabeth Salzer et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Clinical manifestations, course, and outcome of patients with neutralizing anti-interferon-γ autoantibodies and disseminated nontuberculous mycobacterial infections

(2016) Chih-Yu Chi et al.   MEDICINE

Early-Onset Juvenile SLE Associated With a Novel Mutation in Protein Kinase C δ

(2016) Sira Nanthapisal et al.   PEDIATRICS

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

Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections

(2014) Christine Deffert et al.   CELLULAR MICROBIOLOGY

Common Severe Infections in Chronic Granulomatous Disease

(2014) B. E. Marciano et al.   CLINICAL INFECTIOUS DISEASES

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

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

(2011) Jacinta Bustamante et al.   NATURE IMMUNOLOGY

Influence of Neutrophil Defects on Burkholderia cepacia Complex Pathogenesis

(2011) Laura A. Porter et al.   Frontiers in Cellular and Infection Microbiology

Anti-interferon-γ autoantibody in a patient with disseminated Mycobacterium avium complex

(2009) Toshiyuki Koya et al.   JOURNAL OF INFECTION AND CHEMOTHERAPY