Amalia Belfiore

Mutational analysis of the HIV-1 auxiliary protein Vif identifies independent domains important for the physical and functional interaction with HIV-1 reverse transcriptase

G. Maga, C. Bovolenta, R. Lupo, 2009, Nucleic acids research.

2-Hydroxypropyl-β-cyclodextrin strongly improves water solubility and anti-proliferative activity of pyrazolo[3,4-d]pyrimidines Src-Abl dual inhibitors.

E. Dreassi, I. Filippi, S. Schenone, 2010, European journal of medicinal chemistry.

Human DEAD‐box ATPase DDX3 shows a relaxed nucleoside substrate specificity

G. Maga, S. Spadari, R. Franca, 2007, Proteins.

Mutational analysis of the HIV-1 auxiliary protein Vif identifies independent domains important for the physical and functional interaction with HIV-1 reverse transcriptase

G. Maga, C. Bovolenta, R. Lupo, 2014, Nucleic acids research.

Pharmacophore modeling and molecular docking led to the discovery of inhibitors of human immunodeficiency virus-1 replication targeting the human cellular aspartic acid-glutamic acid-alanine-aspartic acid box polypeptide 3.

G. Maga, M. Botta, M. Witvrouw, 2008, Journal of medicinal chemistry.

SMALL MOLECULES SOLVING BIG PROBLEMS: PRESENT AND FUTURE OF DRUG DISCOVERY

Maurizio Botta, Anna Lucia Fallacara, Iuni Margaret Laura Tris, 2018, Journal of the Siena Academy of Sciences.

NNRTI-selected mutations at codon 190 of human immunodeficiency virus type 1 reverse transcriptase decrease susceptibility to stavudine and zidovudine.

F. Baldanti, G. Maga, G. Gerna, 2007, Antiviral research.