Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-gamma-receptor (IFNgammaR1) deficiency: mutational analysis and evaluation of therapeutic options.
about
Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunityIFN-gamma mediates the rejection of haematopoietic stem cells in IFN-gammaR1-deficient hostsA novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.The bacterial pathogen Listeria monocytogenes and the interferon family: type I, type II and type III interferonsClinical consequences of defects in the IL-12-dependent interferon-gamma (IFN-gamma) pathway.Type 1/Type 2 immunity in infectious diseases.Impaired interferon gamma-mediated immunity and susceptibility to mycobacterial infection in childhood.Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds.Susceptibility to mycobacterial infections: the importance of host genetics.In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma.Infections in patients with inherited defects in phagocytic function.Genetic lessons learned from X-linked Mendelian susceptibility to mycobacterial diseases.Mendelian susceptibility to mycobacterial disease in egyptian children.A genetic perspective on granulomatous diseases with an emphasis on mycobacterial infections.Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patientsB-cell lymphoma in a patient with complete interferon gamma receptor 1 deficiencyControl of T helper cell differentiation through cytokine receptor inclusion in the immunological synapse.Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds.Interferon-gamma mediates neuronal killing of intracellular bacteria.Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections.IFN-γR1 defects: Mutation update and description of the IFNGR1 variation database.A case of Listeria monocytogenes endophthalmitis with recurrent inflammation and novel management.Vaccination-related Mycobacterium bovis BCG infection.Clinical and host genetic characteristics of Mendelian susceptibility to mycobacterial diseases in Japan.Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages.Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity.Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiency
P2860
Q26862947-CF0AE644-AAEF-4E42-85B8-F5CEC38E2072Q28755865-3B3BF695-40FC-4095-B519-A11FAAAE8E2CQ30492620-66AB4952-4AAD-4B49-AD77-E3D03B1A3255Q33563711-5D4B1BEF-BED5-435B-BAF5-94CA8F49E5B6Q34022537-FC43641D-35FE-4C66-B1FC-D8B0CF769DFBQ34105379-63955BCB-58FF-4E46-AB63-AB75DEE9EDF4Q34290095-414286BB-F37B-4310-A265-CCFF9CD20AE6Q35046817-530A3E7E-E4CA-49C1-8E0D-4C050E99533BQ35069566-CFDA712A-7551-4822-B8EC-99AB840257F6Q35159906-83961C39-647D-40AE-BE8F-CE9D9B8B3930Q35558806-E928BF6D-E5A5-4430-B178-2FB69F96013CQ35860015-A402177A-F24E-43DF-9457-1C56FC72E5CAQ36033806-3122DAB9-9514-441A-BF6C-15F479224B6CQ36654943-5F34B5B5-C8BC-4D4E-81FE-3BCAD089306CQ36688535-BCA03ADF-287A-41FE-B2FF-58229F36D5D3Q37058863-790D3CAB-7A0D-4ADD-B497-54BCAD92D7F0Q37273309-0C68806B-FDF9-425B-BB7C-03D6902A7208Q37360655-036EF853-835D-4075-A8E6-2E63F32CEC37Q38334374-9687F061-DC79-4F4E-9139-4F3C52169A5BQ38637282-0C526B0C-41C7-469C-9532-499CD28B4D31Q39458875-87BBC549-E93E-4927-B8D4-F225A3275131Q40965644-0E6C722C-5FC1-4BA9-BE3C-A9C5E51AE3B3Q43197657-575DFF07-C517-4D49-89E8-4020E6525735Q45255478-B0F3A6C3-4785-45D9-AAB3-22C8B81FBA29Q47678601-54462AF2-0B03-4090-BE47-598FC74ED054Q47800756-4E322A9E-C063-4E81-8D57-25BB964F8AECQ56940210-FE83C04C-8515-49D7-ADA6-3F4874054A81
P2860
Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-gamma-receptor (IFNgammaR1) deficiency: mutational analysis and evaluation of therapeutic options.
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Listeria monocytogenes and rec ...... uation of therapeutic options.
@ast
Listeria monocytogenes and rec ...... uation of therapeutic options.
@en
type
label
Listeria monocytogenes and rec ...... uation of therapeutic options.
@ast
Listeria monocytogenes and rec ...... uation of therapeutic options.
@en
prefLabel
Listeria monocytogenes and rec ...... uation of therapeutic options.
@ast
Listeria monocytogenes and rec ...... uation of therapeutic options.
@en
P2093
P1476
Listeria monocytogenes and rec ...... uation of therapeutic options.
@en
P2093
Friedrich W
Rösen-Wolff A
Wendisch J
P304
P356
10.1016/S0301-472X(99)00077-6
P577
1999-09-01T00:00:00Z