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S100A9 is a biliary protein marker of disease activity in primary sclerosing cholangitis.
Reinhard L, Rupp C, Riedel HD, Ruppert T, Giese T, Flechtenmacher C, Weiss KH, Kloeters-Plachky P, Stremmel W, Schirmacher P, Sauer P, Gotthardt DN. Reinhard L, et al. Among authors: stremmel w. PLoS One. 2012;7(1):e29821. doi: 10.1371/journal.pone.0029821. Epub 2012 Jan 11. PLoS One. 2012. PMID: 22253789 Free PMC article.
PNPLA3 in end-stage liver disease: alcohol consumption, hepatocellular carcinoma development, and transplantation-free survival.
Friedrich K, Wannhoff A, Kattner S, Brune M, Hov JR, Weiss KH, Antoni C, Dollinger M, Neumann-Haefelin C, Seufferlein T, Schemmer P, Schirmacher P, Stremmel W, Gotthardt DN. Friedrich K, et al. Among authors: stremmel w. J Gastroenterol Hepatol. 2014;29(7):1477-84. doi: 10.1111/jgh.12540. J Gastroenterol Hepatol. 2014. PMID: 25273282
CD14 is associated with biliary stricture formation.
Friedrich K, Smit M, Brune M, Giese T, Rupp C, Wannhoff A, Kloeters P, Leopold Y, Denk GU, Weiss KH, Stremmel W, Sauer P, Hohenester S, Schirmacher P, Schemmer P, Gotthardt DN. Friedrich K, et al. Among authors: stremmel w. Hepatology. 2016 Sep;64(3):843-52. doi: 10.1002/hep.28543. Epub 2016 Apr 20. Hepatology. 2016. PMID: 26970220
Reduction in alkaline phosphatase is associated with longer survival in primary sclerosing cholangitis, independent of dominant stenosis.
Rupp C, Rössler A, Halibasic E, Sauer P, Weiss KH, Friedrich K, Wannhoff A, Stiehl A, Stremmel W, Trauner M, Gotthardt DN. Rupp C, et al. Among authors: stremmel w. Aliment Pharmacol Ther. 2014 Dec;40(11-12):1292-301. doi: 10.1111/apt.12979. Epub 2014 Oct 14. Aliment Pharmacol Ther. 2014. PMID: 25316001 Free article.
A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults.
Gotthardt D, Runz H, Keitel V, Fischer C, Flechtenmacher C, Wirtenberger M, Weiss KH, Imparato S, Braun A, Hemminki K, Stremmel W, Rüschendorf F, Stiehl A, Kubitz R, Burwinkel B, Schirmacher P, Knisely AS, Zschocke J, Sauer P. Gotthardt D, et al. Among authors: stremmel w. Hepatology. 2008 Oct;48(4):1157-66. doi: 10.1002/hep.22485. Hepatology. 2008. PMID: 18781607
Iron metabolism and the role of HFE gene polymorphisms in Wilson disease.
Pfeiffenberger J, Gotthardt DN, Herrmann T, Seessle J, Merle U, Schirmacher P, Stremmel W, Weiss KH. Pfeiffenberger J, et al. Among authors: stremmel w. Liver Int. 2012 Jan;32(1):165-70. doi: 10.1111/j.1478-3231.2011.02661.x. Epub 2011 Oct 17. Liver Int. 2012. PMID: 22098612
680 results