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Inflammasome-independent IL-1β mediates autoinflammatory disease in Pstpip2-deficient mice.
Cassel SL, Janczy JR, Bing X, Wilson SP, Olivier AK, Otero JE, Iwakura Y, Shayakhmetov DM, Bassuk AG, Abu-Amer Y, Brogden KA, Burns TL, Sutterwala FS, Ferguson PJ. Cassel SL, et al. Among authors: ferguson pj. Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):1072-7. doi: 10.1073/pnas.1318685111. Epub 2014 Jan 6. Proc Natl Acad Sci U S A. 2014. PMID: 24395802 Free PMC article.
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles.
Darbro BW, Mahajan VB, Gakhar L, Skeie JM, Campbell E, Wu S, Bing X, Millen KJ, Dobyns WB, Kessler JA, Jalali A, Cremer J, Segre A, Manak JR, Aldinger KA, Suzuki S, Natsume N, Ono M, Hai HD, Viet le T, Loddo S, Valente EM, Bernardini L, Ghonge N, Ferguson PJ, Bassuk AG. Darbro BW, et al. Among authors: ferguson pj. Hum Mutat. 2013 Aug;34(8):1075-9. doi: 10.1002/humu.22351. Epub 2013 May 28. Hum Mutat. 2013. PMID: 23674478 Free PMC article.
Phenotypic Variability in Majeed Syndrome.
Rao AP, Gopalakrishna DB, Bing X, Ferguson PJ. Rao AP, et al. Among authors: ferguson pj. J Rheumatol. 2016 Jun;43(6):1258-9. doi: 10.3899/jrheum.151193. J Rheumatol. 2016. PMID: 27252506 Free PMC article. No abstract available.
Efficacy of anti-IL-1 treatment in Majeed syndrome.
Herlin T, Fiirgaard B, Bjerre M, Kerndrup G, Hasle H, Bing X, Ferguson PJ. Herlin T, et al. Among authors: ferguson pj. Ann Rheum Dis. 2013 Mar;72(3):410-3. doi: 10.1136/annrheumdis-2012-201818. Epub 2012 Oct 20. Ann Rheum Dis. 2013. PMID: 23087183 Free PMC article.
172 results