Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity
about
Severe infectious diseases of childhood as monogenic inborn errors of immunityRegulation of human helper T cell subset differentiation by cytokinesApplication of Flow Cytometry in the Evaluation of Primary ImmunodeficienciesDiagnostic and therapeutic challenges in a child with complete interferon-γ receptor 1 deficiencyHuman TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndromePrimary subacute epiphyseal osteomyelitis caused by Mycobacterium species in young children: a modern diagnostic approach.Microbial Disease Spectrum Linked to a Novel IL-12Rβ1 N-Terminal Signal Peptide Stop-Gain Homozygous Mutation with Paradoxical Receptor Cell-Surface ExpressionMultifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the LiteratureCystic fibrosis carriership and tuberculosis: hints toward an evolutionary selective advantage based on data from the Brazilian territory.Neutrophils in Tuberculosis: Heterogeneity Shapes the Way?ISG15 in Host Defense Against Candida albicans Infection in a Mouse Model of Fungal Keratitis.Cellular and Molecular Defects Underlying Invasive Fungal Infections-Revelations from Endemic Mycoses.The genetic regulation of infant immune responses to vaccination.Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency.Determinants of the Sympatric Host-Pathogen Relationship in Tuberculosis.A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals.In Vivo Molecular Dissection of the Effects of HIV-1 in Active Tuberculosis.Understanding immune protection against tuberculosis using RNA expression profilingType I IFN Signaling Is Dispensable during Secondary Viral InfectionHousehold Contact Screening and Yield of Tuberculosis Cases-A Clinic Based Study in Chennai, South India.IMMUNODEFICIENCIES. Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations.IFN-γ-mediated hematopoietic cell destruction in murine models of immune-mediated bone marrow failure.The introduction of RNA-DNA differences underlies interindividual variation in the human IL12RB1 mRNA repertoire.Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic Intersection.Clinical Immunophenotype at Disease Onset in Previously Healthy Patients With Cryptococcal Meningitis.Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patientsIL-12 drives functional plasticity of human group 2 innate lymphoid cells.Mendelian Susceptibility to Mycobacterial Disease due to IL-12Rβ1 Deficiency in Three Iranian Children.Interferon-gamma-dependent Immunity in Bacillus Calmette-Guérin Vaccine Osteitis Survivors.CD4 T Cell-Derived IFN-γ Plays a Minimal Role in Control of Pulmonary Mycobacterium tuberculosis Infection and Must Be Actively Repressed by PD-1 to Prevent Lethal Disease.Pott's disease in Moroccan children: clinical features and investigation of the interleukin-12/interferon-γ pathway.Missense splice variant (g.20746A>G, p.Ile183Val) of interferon gamma receptor 1 (IFNGR1) coincidental with mycobacterial osteomyelitis - a screen of osteoarticular lesionsClinical manifestations, course, and outcome of patients with neutralizing anti-interferon-γ autoantibodies and disseminated nontuberculous mycobacterial infectionsDisseminated BCG Infectious Disease and Hyperferritinemia in a Patient With a Novel NEMO Mutation.Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.IL-1β, But Not Programed Death-1 and Programed Death Ligand Pathway, Is Critical for the Human Th17 Response to Mycobacterium tuberculosis.Novel Mutation of Interferon-γ Receptor 1 Gene Presenting as Early Life Mycobacterial Bronchial Disease.Chronic mucocutaneous candidiasis disease associated with inborn errors of IL-17 immunity.The IL-17A rs2275913 single nucleotide polymorphism is associated with protection to tuberculosis but related to higher disease severity in Argentina.
P2860
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P2860
Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@ast
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@en
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@nl
type
label
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@ast
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@en
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@nl
prefLabel
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@ast
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@en
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@nl
P2860
P50
P3181
P1476
Mendelian susceptibility to my ...... nborn errors of IFN-γ immunity
@en
P2860
P304
P3181
P356
10.1016/J.SMIM.2014.09.008
P407
P577
2014-12-01T00:00:00Z