Edoardo Nusco

Pozzuoli, Italy

Last Updated: 09/26/2026

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Found 43 publications

TFEB coordinates autophagosome biogenesis and ribophagy during starvation via SQSTM1.

TFEB coordinates autophagosome biogenesis and ribophagy during starvation via SQSTM1.

Journal: Science advances

Published: January 01, 2026

Normal urinary oxalate excretion in 4-hydroxy-2-oxo-glutarate aldolase 1 (HOGA1) deficient mice with AGT expression in peroxisomes and not in mitochondria.

Normal urinary oxalate excretion in 4-hydroxy-2-oxo-glutarate aldolase 1 (HOGA1) deficient mice with AGT expression in peroxisomes and not in mitochondria.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: April 23, 2025

TRPML-1 Dysfunction and Renal Tubulopathy in Mucolipidosis Type IV.

TRPML-1 Dysfunction and Renal Tubulopathy in Mucolipidosis Type IV.

Journal: Journal of the American Society of Nephrology : JASN

Published: July 25, 2024

Hepatocyte delivery of miR-34b/c reduces hepatic stellate cell activation and improves liver fibrosis.

Hepatocyte delivery of miR-34b/c reduces hepatic stellate cell activation and improves liver fibrosis.

Journal: Molecular therapy. Nucleic acids

Published: July 21, 2024

Combined intraocular and intravenous gene delivery for therapy of gyrate atrophy of the choroid and retina.

Combined intraocular and intravenous gene delivery for therapy of gyrate atrophy of the choroid and retina.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: July 07, 2024

TFEB controls syncytiotrophoblast formation and hormone production in placenta.

TFEB controls syncytiotrophoblast formation and hormone production in placenta.

Journal: Cell death and differentiation

Published: May 27, 2024

Impact of liver fibrosis on AAV-mediated gene transfer to mouse hepatocytes.

Impact of liver fibrosis on AAV-mediated gene transfer to mouse hepatocytes.

Journal: Nature communications

Published: March 04, 2024

Safe and effective liver-directed AAV-mediated homology-independent targeted integration in mouse models of inherited diseases.

Safe and effective liver-directed AAV-mediated homology-independent targeted integration in mouse models of inherited diseases.

Journal: Cell reports. Medicine

Published: October 04, 2023

Genome editing without nucleases confers proliferative advantage to edited hepatocytes and corrects Wilson disease.

Genome editing without nucleases confers proliferative advantage to edited hepatocytes and corrects Wilson disease.

Journal: JCI insight

Published: June 27, 2023

Increased expression or activation of TRPML1 reduces hepatic storage of toxic Z alpha-1 antitrypsin.

Increased expression or activation of TRPML1 reduces hepatic storage of toxic Z alpha-1 antitrypsin.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: April 19, 2023

The Amyloid Inhibitor CLR01 Relieves Autophagy and Ameliorates Neuropathology in a Severe Lysosomal Storage Disease.

The Amyloid Inhibitor CLR01 Relieves Autophagy and Ameliorates Neuropathology in a Severe Lysosomal Storage Disease.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: October 19, 2022

Liver-directed gene therapy for ornithine aminotransferase deficiency.

Liver-directed gene therapy for ornithine aminotransferase deficiency.

Journal: EMBO molecular medicine

Published: October 14, 2022

Showing 1-12 of 43

Last Updated: 09/26/2026