Fabio Bertozzi

Genoa, 16163, Italy

Last Updated: 09/26/2026

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Found 24 publications

Molecular targeting of the deubiquitinase USP14 to circumvent cisplatin resistance in ovarian carcinoma and identification of novel inhibitors.

Molecular targeting of the deubiquitinase USP14 to circumvent cisplatin resistance in ovarian carcinoma and identification of novel inhibitors.

Journal: Cancer drug resistance (Alhambra, Calif.)

Published: April 16, 2025

Target Identification with Live-Cell Photoaffinity Labeling and Mechanism of Action Elucidation of ARN23765, a Highly Potent CFTR Corrector.

Target Identification with Live-Cell Photoaffinity Labeling and Mechanism of Action Elucidation of ARN23765, a Highly Potent CFTR Corrector.

Journal: Journal of medicinal chemistry

Published: February 10, 2025

Combined in vivo effect of N-acylethanolamine-hydrolyzing acid amidase and glycogen synthase kinase-3β inhibition to treat multiple sclerosis.

Combined in vivo effect of N-acylethanolamine-hydrolyzing acid amidase and glycogen synthase kinase-3β inhibition to treat multiple sclerosis.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: January 11, 2024

Oxytocin seals the blood-brain barrier, improving 22q11.2 deletion syndrome trajectories.

Oxytocin seals the blood-brain barrier, improving 22q11.2 deletion syndrome trajectories.

Journal: Brain : a journal of neurology

Published: November 10, 2023

Pharmacological potentiators of the calcium signaling cascade identified by high-throughput screening.

Pharmacological potentiators of the calcium signaling cascade identified by high-throughput screening.

Journal: PNAS nexus

Published: July 20, 2022

Editorial: Protein-Protein Interactions: Drug Discovery for the Future.

Editorial: Protein-Protein Interactions: Drug Discovery for the Future.

Journal: Frontiers in chemistry

Published: November 08, 2021

Discovery and SAR Evolution of Pyrazole Azabicyclo[3.2.1]octane Sulfonamides as a Novel Class of Non-Covalent N-Acylethanolamine-Hydrolyzing Acid Amidase (NAAA) Inhibitors for Oral Administration.

Discovery and SAR Evolution of Pyrazole Azabicyclo[3.2.1]octane Sulfonamides as a Novel Class of Non-Covalent N-Acylethanolamine-Hydrolyzing Acid Amidase (NAAA) Inhibitors for Oral Administration.

Journal: Journal of medicinal chemistry

Published: September 01, 2021

Inhibition of N-acylethanolamine-hydrolyzing acid amidase reduces T cell infiltration in a mouse model of multiple sclerosis.

Inhibition of N-acylethanolamine-hydrolyzing acid amidase reduces T cell infiltration in a mouse model of multiple sclerosis.

Journal: Pharmacological research

Published: June 14, 2021

Partial Rescue of F508del-CFTR Stability and Trafficking Defects by Double Corrector Treatment.

Partial Rescue of F508del-CFTR Stability and Trafficking Defects by Double Corrector Treatment.

Journal: International journal of molecular sciences

Published: March 11, 2021

Identification, Structure-Activity Relationship, and Biological Characterization of 2,3,4,5-Tetrahydro-1H-pyrido[4,3-b]indoles as a Novel Class of CFTR Potentiators.

Identification, Structure-Activity Relationship, and Biological Characterization of 2,3,4,5-Tetrahydro-1H-pyrido[4,3-b]indoles as a Novel Class of CFTR Potentiators.

Journal: Journal of medicinal chemistry

Published: September 18, 2020

Identification of a 2,4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaign.

Identification of a 2,4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaign.

Journal: European journal of medicinal chemistry

Published: August 23, 2019

Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel.

Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel.

Journal: Science advances

Published: August 01, 2019

Showing 1-12 of 24

Last Updated: 09/26/2026