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Page 1
Epigenetic activation and memory at a TGFB2 enhancer in systemic sclerosis.
Shin JY, Beckett JD, Bagirzadeh R, Creamer TJ, Shah AA, McMahan Z, Paik JJ, Sampedro MM, MacFarlane EG, Beer MA, Warren D, Wigley FM, Dietz HC. Shin JY, et al. Among authors: wigley fm. Sci Transl Med. 2019 Jun 19;11(497):eaaw0790. doi: 10.1126/scitranslmed.aaw0790. Sci Transl Med. 2019. PMID: 31217334 Free PMC article.
Often forgotten manifestations of systemic sclerosis.
Shah AA, Wigley FM. Shah AA, et al. Among authors: wigley fm. Rheum Dis Clin North Am. 2008 Feb;34(1):221-38; ix. doi: 10.1016/j.rdc.2007.10.002. Rheum Dis Clin North Am. 2008. PMID: 18329542 Review.
Identification of candidate genes in scleroderma-related pulmonary arterial hypertension.
Grigoryev DN, Mathai SC, Fisher MR, Girgis RE, Zaiman AL, Housten-Harris T, Cheadle C, Gao L, Hummers LK, Champion HC, Garcia JG, Wigley FM, Tuder RM, Barnes KC, Hassoun PM. Grigoryev DN, et al. Among authors: wigley fm. Transl Res. 2008 Apr;151(4):197-207. doi: 10.1016/j.trsl.2007.12.010. Epub 2008 Feb 1. Transl Res. 2008. PMID: 18355767 Free PMC article.
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
Loeys BL, Gerber EE, Riegert-Johnson D, Iqbal S, Whiteman P, McConnell V, Chillakuri CR, Macaya D, Coucke PJ, De Paepe A, Judge DP, Wigley F, Davis EC, Mardon HJ, Handford P, Keene DR, Sakai LY, Dietz HC. Loeys BL, et al. Sci Transl Med. 2010 Mar 17;2(23):23ra20. doi: 10.1126/scitranslmed.3000488. Sci Transl Med. 2010. PMID: 20375004 Free PMC article.
My approach to the treatment of scleroderma.
Shah AA, Wigley FM. Shah AA, et al. Among authors: wigley fm. Mayo Clin Proc. 2013 Apr;88(4):377-93. doi: 10.1016/j.mayocp.2013.01.018. Mayo Clin Proc. 2013. PMID: 23541012 Free PMC article. Review.
249 results