Associated Papers
Modelling severe COVID-19 in TLR3-mutated hiPSCs-derived lung organoids.
Latini A et al.
Cell Death Discovery, 2025
Concomitant Ultrarare Mutations in TLR3 and CTPS2 in a Patient with Severe and Recurrent Respiratory Infections in Early Life.
Bougarn S et al.
Journal of Clinical Immunology, 2024
39312089 (PubMed )
Supplement: 10875_2024_1804_MOESM1_ESM.docx
The association of COVID-19 severity and susceptibility and genetic risk factors: A systematic review of the literature.
Ishak A et al.
Gene, 2022
Life-Threatening Enterovirus 71 Encephalitis in Unrelated Children with Autosomal Dominant TLR3 Deficiency.
Kuo CY et al.
Journal of Clinical Immunology, 2022
An overview of human proteins and genes involved in SARS-CoV-2 infection.
Jahanafrooz Z et al.
Gene, 2022
Human genetic basis of severe or critical illness in COVID-19.
Ji XS et al.
Frontiers in Cellular and Infection Microbiology, 2022
Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis.
Chen J et al.
The Journal of Experimental Medicine, 2021
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
Zhang Q et al.
Science (new York, N.y.), 2020
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