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Novel Mutation of Interferon-γ Receptor 1 Gene Presenting as Early Life Mycobacterial Bronchial Disease

https://doi.org/10.1177/2324709616675463
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/pbc.25625openalex-snapshot
Diagnostic and therapeutic challenges in a child with complete Interferon‐γ Receptor 1 deficiency
inferredcites →https://doi.org/10.1016/j.smim.2006.07.010openalex-snapshot
Inborn errors of IL-12/23- and IFN-γ-mediated immunity: molecular, cellular, and clinical features
inferredcites →https://doi.org/10.1016/j.smim.2014.09.008openalex-snapshot
Mendelian susceptibility to mycobacterial disease: Genetic, immunological, and clinical features of inborn errors of IFN-γ immunity
inferredcites →https://doi.org/10.1016/s0140-6736(04)17552-1openalex-snapshot
Clinical features of dominant and recessive interferon γ receptor 1 deficiencies
inferredcites →https://doi.org/10.1016/s0968-0004(00)01561-9openalex-snapshot
Cn3D: sequence and structure views for Entrez
inferredcites →https://doi.org/10.1016/s1473-3099(15)00089-4openalex-snapshot
Host susceptibility to non-tuberculous mycobacterial infections
inferredcites →https://doi.org/10.1038/nmeth.2890openalex-snapshot
MutationTaster2: mutation prediction for the deep-sequencing age
inferredcites →https://doi.org/10.1056/nejm199612263352604openalex-snapshot
Interferon-γ –Receptor Deficiency in an Infant with Fatal Bacille Calmette–Guérin Infection
inferredcites →https://doi.org/10.1111/j.0105-2896.2005.00227.xopenalex-snapshot
Defects in the interferon‐γ and interleukin‐12 pathways

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.5085100openalex-extracted
inferred← citeshttps://doi.org/10.1002/humu.23302openalex-snapshot
IFN-γR1 defects: Mutation update and description of theIFNGR1variation database
inferred← citeshttps://doi.org/10.1007/s10875-019-0593-4openalex-snapshot
Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-820472-6.00112-2openalex-snapshot
Cytokine Receptors
inferred← citeshttps://doi.org/10.1016/j.jctube.2025.100554openalex-snapshot
Analysis of nontuberculous mycobacterial infections in Saudi children from a tertiary care hospital perspective
inferred← citeshttps://doi.org/10.1111/imcb.12210openalex-snapshot
Mendelian susceptibility to mycobacterial disease: 2014–2018 update
inferred← citeshttps://doi.org/10.1155/2020/8836685openalex-snapshot
Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic
inferred← citeshttps://doi.org/10.1182/blood-2017-10-812859openalex-snapshot
Hematopoietic stem cell gene therapy for IFNγR1 deficiency protects mice from mycobacterial infections
inferred← citeshttps://doi.org/10.21518/ms2024-057openalex-snapshot
Interferon gamma as a trigger of chronic viral infections and inflammatory dermatoses
inferred← citeshttps://doi.org/10.3390/clinpract12050082openalex-snapshot
Role of Interferons in Mycobacterium tuberculosis Infection
inferred← citeshttps://doi.org/10.3390/tropicalmed10070202openalex-snapshot
Anti-IFN-γ Autoantibody Syndrome Presenting with Disseminated Nontuberculous Mycobacteria Infections: A Case Series of Therapeutic Implications and Review of Literature
inferred← citeshttps://doi.org/10.70675/f0a50ca5zbb74z4488zb4bez6e36b750a75dopenalex-snapshot
Identification et caractérisation d'une nouvelle forme de défaut partiel récessif héréditaire en JAK1 chez l'homme
inferred← citeshttps://doi.org/10.70962/jhi.20250013openalex-snapshot
A patient with complete IFN-γR1 deficiency and tuberculosis resembling BCG disease
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