Associated Papers
"In silico analysis of human TLR3 missense single nucleotide polymorphisms and their potential association with cancer".
Agarwal M et al.
Scientific Reports, 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
Inborn Errors of Immunity Predisposing to Herpes Simplex Virus Infections of the Central Nervous System.
Skouboe MK et al.
Pathogens (basel, Switzerland), 2023
Life-Threatening Enterovirus 71 Encephalitis in Unrelated Children with Autosomal Dominant TLR3 Deficiency.
Kuo CY et al.
Journal of Clinical Immunology, 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
The role of host genetics in susceptibility to severe viral infections in humans and insights into host genetics of severe COVID-19: A systematic review.
Elhabyan A et al.
Virus Research, 2020
Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis.
Partanen T et al.
Journal of Clinical Immunology, 2020
Severe influenza pneumonitis in children with inherited TLR3 deficiency.
Lim HK et al.
The Journal of Experimental Medicine, 2019
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease.
Aslaksen S et al.
Journal of Translational Autoimmunity, 2019
TLR3 Mutations in Adult Patients With Herpes Simplex Virus and Varicella-Zoster Virus Encephalitis.
Sironi M et al.
The Journal of Infectious Diseases, 2017
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.
Henmyr V et al.
Bmc Medical Genetics, 2017
28228119 (PubMed )
Supplement: 12881_2017_379_MOESM8_ESM.xlsx › TabS4
TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk.
Lim HK et al.
Neurology, 2014
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