B. Wolff

发表

Nortropinyl-arylsulfonylureas as novel, reversible inhibitors of human steroid sulfatase.

P. Nussbaumer, D. Geyl, A. Horvath, 2003, Bioorganic & medicinal chemistry letters.

N-Acyl arylsulfonamides as novel, reversible inhibitors of human steroid sulfatase.

P. Nussbaumer, P. Lehr, B. Wolff, 2005, Bioorganic & medicinal chemistry letters.

1Alpha,25-dihydroxyvitamin D3 decreases DNA binding of nuclear factor-kappaB in human fibroblasts.

B. Wolff, I. Lindley, H. Harant, 1998, FEBS letters.

1α,25‐Dihydroxyvitamin D3 decreases DNA binding of nuclear factor‐κB in human fibroblasts

B. Wolff, I. Lindley, H. Harant, 1998 .

2-(1-adamantyl)-4-(thio)chromenone-6-carboxylic acids: potent reversible inhibitors of human steroid sulfatase.

P. Nussbaumer, A. Horvath, B. Wolff, 2004, Journal of medicinal chemistry.

Chiral-auxiliary-controlled diastereoselectivity in the epoxidation of enecarbamates with DMD and mCPBA.

W. Adam, B. Wolff, Sara G. Bosio, 2003, Organic letters.

Enecarbamates as selective substrates in oxidations: chiral-auxiliary-controlled mode selectivity and diastereoselectivity in the [2+2] cycloaddition and ene reaction of singlet oxygen and in the epoxidation by DMD and mCPBA.

N. Turro, W. Adam, B. Wolff, 2004, The Journal of organic chemistry.

Microtiter plate cellular assay for human steroid sulfatase with fluorescence readout.

P. Nussbaumer, B. Wolff, A. Billich, 2003, Analytical biochemistry.

Inhibition of Vascular Endothelial Growth Factor Cotranslational Translocation by the Cyclopeptolide CAM741

E. Schreiner, S. Maier, J. D. de Vries, 2007, Molecular Pharmacology.

Microbial Conversion Products of Leptomycin B

B. Wolff, Ying Wang, M. Kuhnt, 1998, Applied and Environmental Microbiology.

NOVEL LEPTOMYCINS FROM A STREPTOMYCES STRAIN A92-308902 : INHIBITORS OF THE NUCLEO-CYTOPLASMIC TRANSLOCATION OF THE HIV-1 REGULATORY PROTEIN REV

B. Wolff, J. Sanglier, Ying Wang, 1997 .

Leptomycin B inactivates CRM1/exportin 1 by covalent modification at a cysteine residue in the central conserved region.

N. Kudo, N. Matsumori, H. Taoka, 1999, Proceedings of the National Academy of Sciences of the United States of America.

6-(2-adamantan-2-ylidene-hydroxybenzoxazole)-O-sulfamate: a potent non-steroidal irreversible inhibitor of human steroid sulfatase.

E. Schreiner, A. Winiski, B. Wolff, 2003, Bioorganic & medicinal chemistry letters.

Leptomycin B inhibition of signal-mediated nuclear export by direct binding to CRM1.

M. Yanagida, N. Kudo, E. Schreiner, 1998, Experimental cell research.

Leptomycin B is an inhibitor of nuclear export: inhibition of nucleo-cytoplasmic translocation of the human immunodeficiency virus type 1 (HIV-1) Rev protein and Rev-dependent mRNA.

Y. Wang, B. Wolff, B. Wolff, 1997, Chemistry & biology.

A novel anti‐inflammatory drug, SDZ ASM 981, for the treatment of skin diseases: in vitro pharmacology

A. Winiski, F. Kalthoff, P. Hiestand, 1999, The British journal of dermatology.

6‐(2‐Adamantan‐2‐ylidene‐hydroxybenzoxazole)‐O‐sulfamate: A Potent Non‐Steroidal Irreversible Inhibitor of Human Steroid Sulfatase.

E. Schreiner, A. Winiski, B. Wolff, 2004 .