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Page 1
Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis.
Ferrada MA, Savic S, Cardona DO, Collins JC, Alessi H, Gutierrez-Rodrigues F, Kumar DBU, Wilson L, Goodspeed W, Topilow JS, Paik JJ, Poulter JA, Kermani TA, Koster MJ, Warrington KJ, Cargo C, Tattersall RS, Duncan CJA, Cantor A, Hoffmann P, Payne EM, Bonnekoh H, Krause K, Cowen EW, Calvo KR, Patel BA, Ombrello AK, Kastner DL, Young NS, Werner A, Grayson PC, Beck DB. Ferrada MA, et al. Among authors: topilow js. Blood. 2022 Sep 29;140(13):1496-1506. doi: 10.1182/blood.2022016985. Blood. 2022. PMID: 35793467 Free PMC article.
Novel genetic mutation in myositis-variant of VEXAS syndrome.
Topilow JS, Ospina Cardona D, Beck DB, Ferrada MA, McMahan ZH, Paik JJ. Topilow JS, et al. Rheumatology (Oxford). 2022 Nov 28;61(12):e371-e373. doi: 10.1093/rheumatology/keac356. Rheumatology (Oxford). 2022. PMID: 35713495 Free PMC article. No abstract available.
Reply.
Melamud A, Topilow JS. Melamud A, et al. Among authors: topilow js. Am J Ophthalmol. 2017 Apr;176:262. doi: 10.1016/j.ajo.2017.01.030. Epub 2017 Feb 21. Am J Ophthalmol. 2017. PMID: 28236440 No abstract available.
Reply.
Melamud A, Topilow JS, Cai L, He X. Melamud A, et al. Among authors: topilow js. Am J Ophthalmol. 2016 Sep;169:296-297. doi: 10.1016/j.ajo.2016.06.035. Epub 2016 Jul 25. Am J Ophthalmol. 2016. PMID: 27460815 No abstract available.