M. V. van Dongen

发表

Structure-based screening and design in drug discovery.

Johan Schultz, J. Weigelt, M. Wikström, 2002, Drug discovery today.

The transition from a neutral-pH double helix to a low-pH triple helix induces a conformational switch in the CCCG tetraloop closing a Watson-Crick stem.

C. W. Hilbers, G. A. van der Marel, S. Wijmenga, 1996, Journal of molecular biology.

A small-molecule fusion inhibitor of influenza virus is orally active in mice

I. Wilson, Divita Garg, D. Roymans, 2019, Science.

Unambiguous structure characterization of a DNA-RNA triple helix by 15N- and 13C-filtered NOESY spectroscopy.

C. W. Hilbers, G. A. van der Marel, H. Heus, 1996, Biochemistry.

Structural features of the DNA hairpin d(ATCCTA-GTTA-TAGGAT): formation of a G-A base pair in the loop.

C. W. Hilbers, G. A. van der Marel, S. Wijmenga, 1997, Nucleic acids research.

Solution structure and dynamics of the DNA-binding domain of the adipocyte-transcription factor FREAC-11.

P. Carlsson, S. Enerbäck, M. Wikström, 2000, Journal of molecular biology.

Age‐dependent deamidation of αB‐crystallin

W. D. de Jong, M. V. van Dongen, C. Voorter, 1993 .

Biophysical and physicochemical methods differentiate highly ligand-efficient human D-amino acid oxidase inhibitors.

Chris Oostenbrink, Natalia Markova, Jennifer Venhorst, 2011, European journal of medicinal chemistry.

Potent peptidic fusion inhibitors of influenza virus

I. Wilson, R. Vreeken, Christophe Buyck, 2017, Science.

N'-(arylsulfonyl)pyrazoline-1-carboxamidines as novel, neutral 5-hydroxytryptamine 6 receptor (5-HT₆R) antagonists with unique structural features.

Jennifer Venhorst, J. Venhorst, M. V. van Dongen, 2011, Journal of medicinal chemistry.

Site-selective screening by NMR spectroscopy with labeled amino acid pairs.

Johan Schultz, J. Weigelt, M. Wikström, 2002, Journal of the American Chemical Society.

Site-selective labeling strategies for screening by NMR.

Johan Schultz, J. Weigelt, M. Wikström, 2002, Combinatorial chemistry & high throughput screening.

N'-(arylsulfonyl)pyrazoline-1-carboxamidines as novel, neutral 5-hydroxytryptamine 6 receptor (5-HT₆R) antagonists with unique structural features.

J. Venhorst, M. V. van Dongen, A. van Loevezijn, 2011, Journal of medicinal chemistry.

Structure-based screening as applied to human FABP4: a highly efficient alternative to HTS for hit generation.

Johan Schultz, Stefan Svensson, Thomas Lundbäck, 2002, Journal of the American Chemical Society.

Age-dependent deamidation of alpha B-crystallin.

W. D. de Jong, M. V. van Dongen, C. Voorter, 1993, FEBS letters.