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1.
Mroz, P.A.* et al.: Optimized GIP analogs promote body weight lowering in mice through GIPR agonism not antagonism. Mol. Metab. 20, 51-62 (2019)
2.
Knerr, P.J.* et al.: Optimization of peptide-based polyagonists for treatment of diabetes and obesity. Bioorg. Med. Chem. 26, 2873-2881 (2017)
3.
Finan, B. et al.: Chemical hybridization of glucagon and thyroid hormone optimizes therapeutic Impact for metabolic disease. Cell 167, 843-857.e14 (2016)
4.
Tschöp, M.H. et al.: Unimolecular polypharmacy for treatment of diabetes and obesity. Cell Metab. 24, 51-62 (2016)
5.
Finan, B. et al.: A rationally designed monomeric peptide triagonist corrects obesity and diabetes in rodents. J. Nat. Med. 21, 27-36 (2015)
6.
Finan, B. et al.: Unimolecular dual incretins maximize metabolic benefits in rodents, monkeys, and humans. Sci. Transl. Med. 5:209ra151 (2013)
7.
Habegger, K.M.* et al.: Fibroblast growth factor 21 mediates specific glucagon actions. Diabetes 62, 1453-1463 (2013)
8.
Finan, B. et al.: Targeted estrogen delivery reverses the metabolic syndrome. J. Nat. Med. 18, 1847-1856 (2012)