B. Gsell

发表

Crystal structures of cellular retinoic acid binding proteins I and II in complex with all-trans-retinoic acid and a synthetic retinoid.

T. A. Jones, G. Kleywegt, T. Bergfors, 1995, Structure.

Mapping the conformational space accessible to BACE2 using surface mutants and cocrystals with Fab fragments, Fynomers and Xaperones.

D. Banner, A. Kuglstatter, J. Steyaert, 2013, Acta crystallographica. Section D, Biological crystallography.

Halogen Bonding at the Active Sites of Human Cathepsin L and MEK1 Kinase: Efficient Interactions in Different Environments

Nobuo Shimma, François Diederich, Jörg Benz, 2011, ChemMedChem.

Systematic investigation of halogen bonding in protein-ligand interactions.

François Diederich, Jörg Benz, Bernd Kuhn, 2011, Angewandte Chemie.

HMQC and HSQC experiments with water flip-back optimized for large proteins

H. Senn, B. Gsell, B. Wipf, 1998, Journal of biomolecular NMR.

Characterization of the binding interface between ubiquitin and class I human ubiquitin-conjugating enzyme 2b by multidimensional heteronuclear NMR spectroscopy in solution.

H. Senn, B. Gsell, C. Miyamoto, 1999, Journal of molecular biology.

The formation of diselenide bridges in proteins by incorporation of selenocysteine residues: biosynthesis and characterization of (Se)2-thioredoxin.

A. Böck, C. Baron, B. Gsell, 1994, Biochemistry.

Structural and biophysical characterization of the 40 kDa PEG-interferon-alpha2a and its individual positional isomers.

H. Senn, B. Gsell, A. Ross, 2005, Bioconjugate chemistry.

Identification of potent and selective cathepsin S inhibitors containing different central cyclic scaffolds.

D. Banner, W. Haap, A. Kuglstatter, 2013, Journal of medicinal chemistry.

DNA-Encoded Library-Derived DDR1 Inhibitor Prevents Fibrosis and Renal Function Loss in a Genetic Mouse Model of Alport Syndrome

B. Kuhn, M. Rudolph, M. Prunotto, 2018, ACS chemical biology.

Structure of the human fatty acid synthase KS-MAT didomain as a framework for inhibitor design.

Armin Ruf, Jörg Benz, M. Rudolph, 2010, Journal of molecular biology.

Structural, kinetic, and thermodynamic analysis of the binding of the 40 kDa PEG-interferon-alpha2a and its individual positional isomers to the extracellular domain of the receptor IFNAR2.

Alfred Ross, Walter Huber, P. Gerber, 2005, Bioconjugate chemistry.

A Novel Partial Agonist of Peroxisome Proliferator-Activated Receptor-γ (PPARγ) Recruits PPARγ-Coactivator-1α, Prevents Triglyceride Accumulation, and Potentiates Insulin Signaling in Vitro

Armin Ruf, Hans Peter Märki, Jörg Benz, 2006 .

The crystal structure of carnitine palmitoyltransferase 2 and implications for diabetes treatment.

Jörg Benz, D. Banner, A. Rufer, 2006, Structure.

Structure of the malaria vaccine candidate antigen CyRPA and its complex with a parasite invasion inhibitory antibody

M. Rudolph, A. Rufer, B. Gsell, 2016, eLife.

Synthesis, Characterization, and in vivo Evaluation of a Novel Potent Autotaxin-Inhibitor

J. Hert, P. Mattei, M. Rudolph, 2022, Frontiers in Pharmacology.

The three-dimensional high resolution structure of human interferon alpha-2a determined by heteronuclear NMR spectroscopy in solution.

H. Senn, B. Gsell, B. Wipf, 1997, Journal of molecular biology.

Crystal engineering: deletion mutagenesis of the 24 kDa fragment of the DNA gyrase B subunit from Staphylococcus aureus.

A. D'arcy, G. Dale, B. Gsell, 1999, Acta crystallographica. Section D, Biological crystallography.

Letter to the Editor: Backbone resonance assignment of the N-terminal 24 kDa fragment of the gyrase B subunit from S. aureus complexed with novobiocin

H. Senn, B. Gsell, W. Klaus, 2000, Journal of biomolecular NMR.

A novel partial agonist of peroxisome proliferator-activated receptor-gamma (PPARgamma) recruits PPARgamma-coactivator-1alpha, prevents triglyceride accumulation, and potentiates insulin signaling in vitro.

Armin Ruf, Hans Peter Märki, Jörg Benz, 2006, Molecular endocrinology.

Structural basis for the cyclophilin A binding affinity and immunosuppressive potency of E-ISA247 (voclosporin)

A. Kuglstatter, M. Hennig, B. Gsell, 2011, Acta crystallographica. Section D, Biological crystallography.

Structure of the malaria vaccine candidate antigen CyRPA and its complex with a parasite invasion inhibitory antibody

M. Rudolph, A. Rufer, B. Gsell, 2017, eLife.

Generation of an antibody toolbox to characterize hERG.

M. Hennig, B. Gsell, M. Grütter, 2013, Biochemical and biophysical research communications.

Biological Crystallography Structural Basis for the Cyclophilin a Binding Affinity and Immunosuppressive Potency of E-isa247 (voclosporin)

A. Kuglstatter, M. Hennig, B. Gsell, 2022 .

A Novel Partial Agonist of Peroxisome Proliferator-Activated Receptor- (cid:1) (PPAR (cid:1) ) Recruits PPAR (cid:1) -Coactivator-1 (cid:2) , Prevents Triglyceride Accumulation, and Potentiates Insulin Signaling in Vitro

B. Kuhn, A. Rufer, B. Gsell, 2006 .