Associated Papers
Imetelstat-mediated alterations in fatty acid metabolism to induce ferroptosis as a therapeutic strategy for acute myeloid leukemia.
Bruedigam C et al.
Nature Cancer, 2024
37904045 (PubMed )
Supplement: 43018_2023_653_MOESM22_ESM.xlsx › Extended_Data_Fig._9c_HemePACT
Whole genome sequencing identifies novel genetic mutations in patients with eczema herpeticum.
Bin L et al.
Allergy, 2021
IFN-γR1 defects: Mutation update and description of the IFNGR1 variation database.
van de Vosse E et al.
Human Mutation, 2017
No significant impact of IFN-γ pathway gene variants on tuberculosis susceptibility in a West African population.
Meyer CG et al.
European Journal of Human Genetics : Ejhg, 2016
Targeted deep sequencing identifies rare loss-of-function variants in IFNGR1 for risk of atopic dermatitis complicated by eczema herpeticum.
Gao L et al.
The Journal of Allergy and Clinical Immunology, 2015
Evolutionary genetics evidence of an essential, nonredundant role of the IFN-γ pathway in protective immunity.
Manry J et al.
Human Mutation, 2011
Functional analysis of naturally occurring amino acid substitutions in human IFN-gammaR1.
van de Wetering D et al.
Molecular Immunology, 2010
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