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The Journal of Experimental Medicine|February 27, 2025
The common HAQ STING allele prevents clinical penetrance of COPA syndromeNoa Simchoni, Shogo Koide, Maryel Likhite, et al.
The Journal of Rheumatology|November 15, 2025
Evaluation of Health Disparities in Outcomes of Patients With Juvenile Idiopathic ArthritisJulia G Harris, Jade H Singleton, Tracy V Ting, et al.
Nature Communications|April 4, 2017
Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory diseaseWalter H A Kahr, Fred G Pluthero, Abdul Elkadri, et al.
The Journal of Rheumatology|February 2, 2022
Consensus Approach to a Treat-to-target Strategy in Juvenile Idiopathic Arthritis Care: Report From the 2020 PR-COIN Consensus ConferenceTala El Tal, Meghan E Ryan, Brian M Feldman, et al.
Nature Genetics|September 15, 2014
An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndromeScott W Canna, Adriana A de Jesus, Sushanth Gouni, et al.
Nature Genetics|November 5, 1999
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndromeJ Marcelino, J D Carpten, W M Suwairi, et al.
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