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The Journal of Experimental Medicine|March 7, 2023
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumoniaAna García-García, Rebeca Pérez de Diego, Carlos Flores, et al.
Nature Immunology|April 12, 2024
Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiencyHirotsugu Oda, Kalpana Manthiram, Pallavi Pimpale Chavan, et al.
Medrxiv : the Preprint Server for Health Sciences|November 3, 2022
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, et al.
Science (New York, N.Y.)|September 25, 2020
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19Qian Zhang, Paul Bastard, Zhiyong Liu, et al.
Genome Medicine|April 5, 2023
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, et al.
The Journal of Experimental Medicine|July 6, 2011
Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasisLuyan Liu, Satoshi Okada, Xiao-Fei Kong, et al.
The Journal of Experimental Medicine|March 25, 2020
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Science (New York, N.Y.)|May 19, 2022
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxinAndrás N Spaan, Anna-Lena Neehus, Emmanuel Laplantine, et al.
The Journal of Experimental Medicine|September 12, 2022
Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiencyMasato Ogishi, Andrés Augusto Arias, Rui Yang, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2016
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 casesFrancesca Conti, Saul Oswaldo Lugo-Reyes, Lizbeth Blancas Galicia, et al.
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