Lorenzo Stella

Peptides at work: from structure to applications

Ettore Benedetti, Kyung-Soo Hahm, Lorenzo Stella, 2011, Journal of peptide science : an official publication of the European Peptide Society.

Fluorescence quenching and ligand binding: A critical discussion of a popular methodology

Lorenzo Stella, Marco van de Weert, L. Stella, 2011 .

Counteracting Effects Operating on Src Homology 2 Domain-containing Protein-tyrosine Phosphatase 2 (SHP2) Function Drive Selection of the Recurrent Y62D and Y63C Substitutions in Noonan Syndrome*♦

Gianni Cesareni, Luisa Castagnoli, Antonio Palleschi, 2012, The Journal of Biological Chemistry.

Macrophage sensing of single-walled carbon nanotubes via Toll-like receptors

Sanjay Mathur, Riitta Lahesmaa, Bengt Fadeel, 2018, Scientific Reports.

Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies

Gabriele Gillessen-Kaesbach, Maria Kousi, Alessandro Bruselles, 2015, American journal of human genetics.

Nano-bio interactions: a neutrophil-centric view

Bengt Fadeel, Lucia Gemma Delogu, Paolo Calligari, 2019, Cell Death & Disease.

Analysing protein energy data by a stochastic model for cooperative interactions: comparison and characterization of cooperativity

Luigi Accardi, Mario Abundo, Nicola Rosato, 2002, Journal of mathematical biology.

A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome.

Claudio Carta, Bruno Dallapiccola, Bruce D Gelb, 2012, American journal of human genetics.

Modeling cellular compartmentation in one‐carbon metabolism

Marco Scotti, Lorenzo Stella, L. Stella, 2013, Wiley interdisciplinary reviews. Systems biology and medicine.

7-Nitro-2,1,3-benzoxadiazole Derivatives, a New Class of Suicide Inhibitors for Glutathione S-Transferases

Giovanni Antonini, Lorenzo Stella, G. Filomeni, 2005, Journal of Biological Chemistry.

Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome

Monia Magliozzi, Bruno Dallapiccola, Alessandro Sartorio, 2017, Human mutation.