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The Journal of Experimental Medicine|July 30, 2020
Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signalingAlice Lepelley, Maria José Martin-Niclós, Melvin Le Bihan, et al.Rheumatology (Oxford, England)|November 23, 2019
Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-α signallingIsabelle Melki, Hervé Devilliers, Cyril Gitiaux, et al.Journal of Clinical Immunology|December 5, 2022
Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation BiomarkersMathilde Labouret, Stefania Costi, Vincent Bondet, et al.Journal of Clinical Immunology|January 7, 2021
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I InterferonopathiesLorenzo Lodi, Isabelle Melki, Vincent Bondet, et al.The Journal of Experimental Medicine|March 10, 2026
The STING HAQ haplotype and clinical non-penetrance in COPA syndromeClémence David, Tifenn Wauquier, Alix de Becdelièvre, et al.The Journal of Allergy and Clinical Immunology|June 21, 2023
Successful treatment of JAK1-associated inflammatory diseaseAntoine Fayand, Véronique Hentgen, Céline Posseme, et al.The Journal of Experimental Medicine|April 20, 2017
Detection of interferon alpha protein reveals differential levels and cellular sources in diseaseMathieu P Rodero, Jérémie Decalf, Vincent Bondet, et al.Blood|July 29, 2025
Impaired cytotoxic function and exhausted phenotype of natural killer cells in VEXAS syndromePaul Breillat, Francesco Carbone, Emilie Lereclus, et al.Journal of Clinical Immunology|May 12, 2023
JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach StudyMarie-Louise Frémond, Marie Hully, Benjamin Fournier, et al.Science Immunology|December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.Pageof 19