Stefano Bonatti

Naples, Italy

Last Updated: 09/26/2026

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Found 15 publications

Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.

Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.

Journal: Scientific reports

Published: June 24, 2020

Unconventional secretion of α-Crystallin B requires the Autophagic pathway and is controlled by phosphorylation of its serine 59 residue.

Unconventional secretion of α-Crystallin B requires the Autophagic pathway and is controlled by phosphorylation of its serine 59 residue.

Journal: Scientific reports

Published: January 24, 2019

An αB-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population.

An αB-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population.

Journal: International journal of molecular sciences

Published: May 25, 2018

Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.

Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.

Journal: Scientific reports

Published: January 22, 2018

Differential phosphorylation-based regulation of αB-crystallin chaperone activity for multipass transmembrane proteins.

Differential phosphorylation-based regulation of αB-crystallin chaperone activity for multipass transmembrane proteins.

Journal: Biochemical and biophysical research communications

Published: August 22, 2016

Adenosine plasma level correlates with homocysteine and uric acid concentrations in patients with coronary artery disease.

Adenosine plasma level correlates with homocysteine and uric acid concentrations in patients with coronary artery disease.

Journal: Canadian journal of physiology and pharmacology

Published: January 15, 2016

Pharmacological folding chaperones act as allosteric ligands of Frizzled4.

Pharmacological folding chaperones act as allosteric ligands of Frizzled4.

Journal: Nature chemical biology

Published: July 18, 2014

ER reorganization is remarkably induced in COS-7 cells accumulating transmembrane protein receptors not competent for export from the endoplasmic reticulum.

ER reorganization is remarkably induced in COS-7 cells accumulating transmembrane protein receptors not competent for export from the endoplasmic reticulum.

Journal: The Journal of membrane biology

Published: May 27, 2014

Screening in planarians identifies MORN2 as a key component in LC3-associated phagocytosis and resistance to bacterial infection.

Screening in planarians identifies MORN2 as a key component in LC3-associated phagocytosis and resistance to bacterial infection.

Journal: Cell host & microbe

Published: January 13, 2014

The cytosolic chaperone α-crystallin B rescues folding and compartmentalization of misfolded multispan transmembrane proteins.

The cytosolic chaperone α-crystallin B rescues folding and compartmentalization of misfolded multispan transmembrane proteins.

Journal: Journal of cell science

Published: July 12, 2013

Familial exudative vitreoretinopathy caused by a homozygous mutation in TSPAN12 in a cystic fibrosis infant.

Familial exudative vitreoretinopathy caused by a homozygous mutation in TSPAN12 in a cystic fibrosis infant.

Journal: Ophthalmic genetics

Published: July 10, 2013

A disorder-to-order structural transition in the COOH-tail of Fz4 determines misfolding of the L501fsX533-Fz4 mutant.

A disorder-to-order structural transition in the COOH-tail of Fz4 determines misfolding of the L501fsX533-Fz4 mutant.

Journal: Scientific reports

Published: May 28, 2013

Showing 1-12 of 15

Last Updated: 09/26/2026