Barbara Renga

发表

Structure-based drug design targeting the cell membrane receptor GPBAR1: exploiting the bile acid scaffold towards selective agonism

Ettore Novellino, Vittorio Limongelli, Francesco Saverio Di Leva, 2015, Scientific Reports.

Discovery of sulfated sterols from marine invertebrates as a new class of marine natural antagonists of farnesoid-X-receptor.

Giuseppe Bifulco, G. Bifulco, V. Sepe, 2011, Journal of medicinal chemistry.

Farnesoid X receptor suppresses constitutive androstane receptor activity at the multidrug resistance protein-4 promoter.

Marco Migliorati, E. Distrutti, S. Fiorucci, 2011, Biochimica et biophysica acta.