Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds
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Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunityVaccines against invasive Salmonella disease: current status and future directionsIL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation databaseThe IL-23-IL-17 immune axis: from mechanisms to therapeutic testing'"Why me, why now?" Using clinical immunology and epidemiology to explain who gets nontuberculous mycobacterial infectionCancers Related to Immunodeficiencies: Update and PerspectivesHGCS: an online tool for prioritizing disease-causing gene variants by biological distancePrimary immunodeficiencies underlying fungal infectionsThe serodominant secreted effector protein of Salmonella, SseB, is a strong CD4 antigen containing an immunodominant epitope presented by diverse HLA class II allelesMolecular confirmation of Bacillus Calmette Guerin vaccine related adverse events among Saudi Arabian children.Mycobacterium simiae infection in two unrelated patients with different forms of inherited IFN-γR2 deficiency.IL12Rβ1ΔTM is a secreted product of il12rb1 that promotes control of extrapulmonary tuberculosisInherited and acquired immunodeficiencies underlying tuberculosis in childhood.Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisFactors Associated with Non-typhoidal Salmonella Bacteremia versus Typhoidal Salmonella Bacteremia in Patients Presenting for Care in an Urban Diarrheal Disease Hospital in BangladeshMRSA Infections in HIV-Infected People Are Associated with Decreased MRSA-Specific Th1 Immunity.The introduction of RNA-DNA differences underlies interindividual variation in the human IL12RB1 mRNA repertoire.A genetic perspective on granulomatous diseases with an emphasis on mycobacterial infections.Mendelian Susceptibility to Mycobacterial Disease due to IL-12Rβ1 Deficiency in Three Iranian Children.Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+ T cells into distinct effector subsets.Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis.Chronic mucocutaneous candidiasis disease associated with inborn errors of IL-17 immunity.Congenital IL-12R1β receptor deficiency and thrombophilia in a girl homozygous for an IL12RB1 mutation and compound heterozygous for MTFHR mutations: A case report and literature reviewHost genomics in infectious diseases.Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example.ICON: the early diagnosis of congenital immunodeficiencies.Cytokine immunomodulation for the treatment of infectious diseases: lessons from primary immunodeficiencies.Host genetics of invasive Aspergillus and Candida infections.Genetic susceptibility to invasive Salmonella disease.The role of cytokine deficiencies and cytokine autoantibodies in clinical dermatology.A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients.The Goldilocks model of immune symbiosis with Mycobacteria and Candida colonizers.Cytokine-Mediated Regulation of Human Lymphocyte Development and Function: Insights from Primary Immunodeficiencies.Chronic Disseminated Salmonellosis in a Patient with Interleukin- 12p40 Deficiency.Evaluation of IL-12RB1, IL-12B, CXCR-3 and IL-17a expression in cases affected by a non-healing form of cutaneous leishmaniasis: an observational study design.Mendelian Susceptibility to Mycobacterial Disease due to IL-12Rβ1 Deficiency in Three Iranian Children.Altered Immune Activation and IL-23 Signaling in Response to Candida albicans in Autoimmune Polyendocrine Syndrome Type 1Recurrent Burkholderia gladioli suppurative lymphadenitis associated with neutralizing anti-IL-12p70 autoantibodies.Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients.
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Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on March 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Inherited IL-12p40 deficiency: ...... f 49 patients from 30 kindreds
@en
Inherited IL-12p40 deficiency: ...... 49 patients from 30 kindreds.
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type
label
Inherited IL-12p40 deficiency: ...... f 49 patients from 30 kindreds
@en
Inherited IL-12p40 deficiency: ...... 49 patients from 30 kindreds.
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prefLabel
Inherited IL-12p40 deficiency: ...... f 49 patients from 30 kindreds
@en
Inherited IL-12p40 deficiency: ...... 49 patients from 30 kindreds.
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Inherited IL-12p40 deficiency: ...... f 49 patients from 30 kindreds
@en
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Abdullah Alangari
Andrew J Pollard
Arina Samarina
Bee Wah Lee
Belinda Murugasu
Carolina Prando
Davood Mansouri
Dinakantha S Kumararatne
Emadia Alaki
Eman Al Idrissi
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P304
P356
10.1097/MD.0B013E31828A01F9
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P577
2013-03-01T00:00:00Z