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Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|August 2, 2006
Preliminary characterization of (nucleoside-2'-O-)-methyltransferase crystals from Meaban and Yokose flavivirusesEloise Mastrangelo, Michela Bollati, Mario Milani, et al.
ACS Medicinal Chemistry Letters|May 22, 2020
Pyridobenzothiazolones Exert Potent Anti-Dengue Activity by Hampering Multiple Functions of NS5 PolymeraseRolando Cannalire, Kitti Wing Ki Chan, Maria Sole Burali, et al.
Viruses|June 24, 2022
Virucidal Activity of the Pyridobenzothiazolone Derivative HeE1-17Y against Enveloped RNA VirusesRafaela Milan Bonotto, Francesco Bonì, Mario Milani, et al.
Computational and Structural Biotechnology Journal|December 23, 2021
A novel hotspot of gelsolin instability triggers an alternative mechanism of amyloid aggregationMichela Bollati, Luisa Diomede, Toni Giorgino, et al.
ACS Medicinal Chemistry Letters|October 16, 2020
Discovery of Zika Virus NS2B/NS3 Inhibitors That Prevent Mice from Life-Threatening Infection and Brain DamageAntonio Coluccia, Michela Puxeddu, Marianna Nalli, et al.
Nature Communications|August 2, 2020
Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral SclerosisLuca Muzio, Riccardo Sirtori, Davide Gornati, et al.
Journal of Medicinal Chemistry|June 7, 2021
Synthesis and Characterization of Novel Mono- and Bis-Guanyl Hydrazones as Potent and Selective ASIC1 Inhibitors Able to Reduce Brain Ischemic InsultDavide Gornati, Roselia Ciccone, Antonio Vinciguerra, et al.
Scientific Reports|August 6, 2025
Identification of new selective CD36 inhibitors to potentiate HER2-targeted therapy in HER2-positive breast cancerLorenzo Castagnoli, Francesco Bonì, Martina Bigliardi, et al.
Bioorganic & Medicinal Chemistry|October 16, 2012
Dimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part II: Structural and biological characterizationDaniele Lecis, Eloise Mastrangelo, Laura Belvisi, et al.
ACS Infectious Diseases|August 3, 2024
4-(3-Phenylsulfonylindol-2-yl)-1-(pyridin-2-yl)piperazinyl-methanones as Potent Inhibitors of both SARS-CoV-2 and HCoV-OC43 VirusesMichela Puxeddu, Manuela Donalisio, Joachim Jakob Bugert, et al.
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