Meloxicam inhibits STING phosphorylation and alleviates intracellular DNA-mediated autoimmune responses by Yu Yu, Miao Wang, Xiao-Wei Li, Jie Mao, Ying-Jie Zhu, Na Wang, Le-Hua Yin, Zeng-Lin Guo, Hong Cai, Tao Li, Ting-Ting Liang, Jiuwei Cui, Tao Zhou

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Typing TREX1 gene in patients with systemic lupus erythematosus by M. Fredi, M. Bianchi, L. Andreoli, G. Greco, I. Olivieri, S. Orcesi, E. Fazzi, C. Cereda, A. Tincani

Subjects: “…TREX1, Novel variation, Neuropsychiatric systemic lupus erythematosus.…”
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Deficiency of Trex1 leads to spontaneous development of type 1 diabetes by Jiang-Man Zhao, Zhi-Hui Su, Qiu-Ying Han, Miao Wang, Xin Liu, Jing Li, Shao-Yi Huang, Jing Chen, Xiao-Wei Li, Xia-Ying Chen, Zeng-Lin Guo, Shuai Jiang, Jie Pan, Tao Li, Wen Xue, Tao Zhou

Subjects: “…TREX1…”
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Safeguard against DNA sensing: The role of TREX1 in HIV-1 infection and autoimmune diseases by Nan eYan, Maroof eHasan

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Retinal vasculopathy with cerebral leukoencephalopathy with TREX1 mutation: a rare entity with a new mutation by Michela Giacoma Pin, Lucia Corrado, Gionata Strigaro, Andrea Bianco, Mattia Bellan, Claudio Musetti, Letizia Mazzini, Roberto Cantello, Sandra D’Alfonso, Domizia Vecchio

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Neonatal onset Aicardi-Goutières syndrome with congenital corneal edema, expanding the phenotype by Romit Jain, Siva Narayana Reddy, Sai Sankeerth Rao Koneru, Ramesh Konanki

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Preimplantation genetic testing for Aicardi–Goutières syndrome induced by novel compound heterozygous mutations of TREX1: an unaffected live birth by Huiling Xu, Jiajie Pu, Suiling Lin, Rui Hu, Jilong Yao, Xuemei Li

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An autoimmune disease prevented by anti-retroviral drugs by Beck-Engeser Gabriele B, Eilat Dan, Wabl Matthias

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AIM2-Like Receptors Positively and Negatively Regulate the Interferon Response Induced by Cytosolic DNA by Yuki Nakaya, Jingtao Lilue, Spyridon Stavrou, Eileen A. Moran, Susan R. Ross

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Case report: Durable response to ruxolitinib in a child with TREX1-related disorder by Yasir Bin Khathlan, Sajdi Almutairi, Fahad B. Albadr, Abdullah A. Alangari, Abdulrahman Alsultan, Abdulrahman Alsultan

Subjects: “…TREX1 gene…”
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The Expression Levels of <i>TREX1</i> and IFN-α Are Associated with Immune Reconstitution in HIV-1-Infected Individuals by Maria Alice Freitas Queiroz, Allysson Quintino Tenório de Oliveira, Tuane Carolina Ferreira Moura, Wandrey Roberto dos Santos Brito, Emmanuelle Giuliana Mendes Santana, Lorena Leticia Peixoto de Lima, Felipe Teixeira Lopes, Carlos David Araújo Bichara, Ednelza da Silva Graça Amoras, Ricardo Ishak, Izaura Maria Vieira Cayres Vallinoto, Antonio Carlos Rosário Vallinoto

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Novel heterozygous TREX1 mutation in a juvenile systemic lupus erythematosus patient with severe cutaneous involvement treated successfully with Jak-inhibitors: a case report by Martina Rossano, Emilio Amleto Conti, Paola Bocca, Stefano Volpi, Stefano Volpi, Antonio Mastrangelo, Riccardo Cavalli, Marco Gattorno, Francesca Minoia, Giovanni Filocamo

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Case Report: Aicardi-Goutières Syndrome Caused by Novel TREX1 Variants by De Wu, Liwei Fang, Ting Huang, Songcheng Ying

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Genome Replication Is Associated With Release of Immunogenic DNA Waste by Nadja Schubert, Tina Schumann, Elena Daum, Karolin Flade, Yan Ge, Lara Hagedorn, Winfried Edelmann, Luise Müller, Marc Schmitz, Marc Schmitz, Marc Schmitz, Gunnar Kuut, Veit Hornung, Rayk Behrendt, Rayk Behrendt, Axel Roers, Axel Roers

Subjects: “…Trex1…”
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Type I interferonopathies with novel compound heterozygous TREX1 mutations in two siblings with different symptoms responded to tofacitinib by Shiyu Zhang, Jiaxing Song, Yuyan Yang, Huilei Miao, Lu Yang, Yuehua Liu, Xue Zhang, Yaping Liu, Tao Wang

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A rare case of occlusive juxtafoveolar retinal telangiectasias associated with lesions of the central nervous system: A cerebroretinal vasculopathy like phenotype without mutations... by Mark P. Seraly, Karim H. Badawi, Sumeet K. Gupta, Nabil M. Jabbour, Brian Ellis, Monique Leys

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Familial chilblain lupus due to a novel mutation in TREX1 associated with Aicardi–Goutie’res syndrome by Cuili Yi, Qiyuan Li, Jihong Xiao

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Case report: JAK inhibition as promising treatment option of fatal RVCLS due to TREX1 mutation (pVAL235Glyfs*6) by Friederike Ufer, Susanne M. Ziegler, Marcus Altfeld, Manuel A. Friese

Subjects: “…TREX1…”
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Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations in conjunction with systemic lupus erythematosus: Missed diagnosis or misdiagnosis? by Xinhui Wang, Li Su, Jinming Han, Yilai Han, Yunsi Yin, Jiancheng Huang, Yi Tang, Yi Zhao, Qi Qin

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The Last Chance Saloon by Ye Hong, Hongtao Zhang, Anton Gartner

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