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Identification of a series of highly potent activators of the Nurr1 signaling pathway.
Bioorg Med Chem Lett. 2007 Jan 1;17(1):193-6. doi: 10.1016/j.bmcl.2006.09.062. Epub 2006 Oct 10.
Bioorg Med Chem Lett. 2007.
PMID: 17035009
Acyl dipeptides as reversible caspase inhibitors. Part 2: further optimization.
Linton SD, Karanewsky DS, Ternansky RJ, Chen N, Guo X, Jahangiri KG, Kalish VJ, Meduna SP, Robinson ED, Ullman BR, Wu JC, Pham B, Kodandapani L, Smidt R, Diaz JL, Fritz LC, von Krosigk U, Roggo S, Schmitz A, Tomaselli KJ.
Linton SD, et al. Among authors: von krosigk u.
Bioorg Med Chem Lett. 2002 Oct 21;12(20):2973-5. doi: 10.1016/s0960-894x(02)00630-3.
Bioorg Med Chem Lett. 2002.
PMID: 12270186
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Redesigning nucleic acids.
Benner SA, Battersby TR, Eschgfaller B, Hutter D, Kodra JT, Lutz S, Arslan T, Baschlin DK, Blattler M, Egli M, Hammer C, Held HA, Horlacher J, Huang Z, Hyrup B, Jenny TF, Jurczyk SC, Konig M, von Krosigk U, Lutz MJ, MacPherson LJ, Moroney SE, Muller E, Nambiar KP, Piccirilli JA, Switzer CY, Vogel JJ, Richert C, Roughton AL, Schmidt J, Schneider KC, Stackhouse J.
Benner SA, et al. Among authors: von krosigk u.
Pure Appl Chem. 1998 Feb;70(2):263-6. doi: 10.1351/pac199870020263.
Pure Appl Chem. 1998.
PMID: 11542721
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