Mafalda Concilli

Pharmacoproteomics pinpoints HSP70 interaction for correction of the most frequent Wilson disease-causing mutant of ATP7B.

D. di Bernardo, F. Napolitano, Mario Renda, 2020, Proceedings of the National Academy of Sciences of the United States of America.

Wilson Disease Protein ATP7B Utilizes Lysosomal Exocytosis to Maintain Copper Homeostasis

Andrea Ballabio, Christopher J. Chang, Simona Iacobacci, 2014, Developmental cell.

Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis.

G. Kroemer, H. Zischka, B. Franco, 2019, Gastroenterology.

Identification of p38 MAPK and JNK as new targets for correction of Wilson disease‐causing ATP7B mutants

A. Luini, B. van de Sluis, M. Monti, 2016, Hepatology.

The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders

Y. Aulchenko, A. Watson, Shan Zhu, 2016, Disease Models & Mechanisms.

Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content

Laura K. Palmer, Blaine R. Roberts, V. Faundez, 2020, The Journal of Neuroscience.

A systems biology approach reveals new endoplasmic reticulum-associated targets for the correction of the ATP7B mutant causing Wilson disease.

R. Polishchuk, A. Carissimo, G. Chesi, 2016, Metallomics : integrated biometal science.

University of Groningen The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers

Y. Aulchenko, A. Watson, Shan Zhu, 2016 .