Dr. Christina Lamers
Assistentin / PostDoc

Christina Lamers

Philosophisch-Naturwissenschaftliche Fakultät

Departement Pharmazeutische Wissenschaften

Molekulare Pharmazie

Assistentin / PostDoc

Klingelbergstrasse 50
4056 Basel

Tel. +41 61 207 15 56

Curriculum Vitae

Christina Lamers graduated in pharmacy in 2008 at the Goethe-University of Frankfurt/Main, Germany. Her practical year she spent 6 month at Merz Consumer Care, Frankfurt/Main before she got licensed as pharmacist in 2009. She was PhD student from 2010-2014 in the group of Prof. Manfred Schubert-Zsilavecz at the Pharmaceutical Chemistry Department of Goethe-University Frankfurt/Main. In 2014 she defended her PhD thesis titles “Synthesis and characterization of fatty acid mimetics as ligands for nuclear receptors PPARs and FXR”. From 2015 – 2017 she worked as a post-doctoral fellow on phage display evolved bicyclic peptides in the lab of Prof. Christian Heinis at EPFL, Switzerland. During this postdoc she won a Marie-Curie individual fellowship. In November 2017 she joined the group of Prof. Daniel Ricklin as post-doctoral fellow at the Institute of Molecular Pharmacy at the University Basel.


Flesch, D., Cheung, S.-Y., Schmidt, J., Gabler, M., Heitel, P., Kramer, J., Kaiser, A., Hartmann, M., Lindner, M., Lüddens-Dämgen, K., Heering, J., Lamers, C., Lüddens, H., Wurglics, M., Proschak, E., Schubert-Zsilavecz, M. und Merk, D. (2017) «Nonacidic Farnesoid X Receptor Modulators», Journal of Medicinal Chemistry, 60(16), S. 7199-7205. doi: 10.1021/acs.jmedchem.7b00903.   edoc
Lamers, C., Merk, D., Gabler, M., Flesch, D., Kaiser, A. und Schubert-Zsilavecz, M. (2016) «SAR studies on FXR modulators led to the discovery of the first combined FXR antagonistic/TGR5 agonistic compound», Future medicinal chemistry, 8(2), S. 133-148. doi: 10.4155/fmc.15.178.   
Blöcher, R., Lamers, C., Wittmann, S. K., Merk, D., Hartmann, M., Weizel, L., Diehl, O., Brüggerhoff, A., Boß, M., Kaiser, A., Schader, T., Göbel, T., Grundmann, M., Angioni, C., Heering, J., Geisslinger, G., Wurglics, M., Kostenis, E., Brüne, B., Steinhilber, D., Schubert-Zsilavecz, M., Kahnt, A. S. und Proschak, E. (2016) «N-Benzylbenzamides: A Novel Merged Scaffold for Orally Available Dual Soluble Epoxide Hydrolase/Peroxisome Proliferator-Activated Receptor γ Modulators», Journal of medicinal chemistry, 59(1), S. 61-81. doi: 10.1021/acs.jmedchem.5b01239.