Alessandro Amati

Bari, 70124, Italy

Last Updated: 09/26/2026

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Found 13 publications

Mitochondrial dysfunction, metabolic quiescence and premature senescence in CMT4B3 fibroblasts.

Mitochondrial dysfunction, metabolic quiescence and premature senescence in CMT4B3 fibroblasts.

Journal: Human molecular genetics

Published: May 19, 2026

Myo-Inositol modulates AKT signalling, mitochondrial protein expression and intracellular Ca²⁺dynamics in human dermal fibroblasts.

Myo-Inositol modulates AKT signalling, mitochondrial protein expression and intracellular Ca²⁺dynamics in human dermal fibroblasts.

Journal: Scientific reports

Published: August 14, 2025

Selective mitophagy activation and protein aggregate accumulation in MTMR5/SBF1-deficient fibroblasts.

Selective mitophagy activation and protein aggregate accumulation in MTMR5/SBF1-deficient fibroblasts.

Journal: Life sciences

Published: July 29, 2025

The Balance of MFN2 and OPA1 in Mitochondrial Dynamics, Cellular Homeostasis, and Disease.

The Balance of MFN2 and OPA1 in Mitochondrial Dynamics, Cellular Homeostasis, and Disease.

Journal: Biomolecules

Published: February 18, 2025

A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P.

A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P.

Journal: Clinical neurology and neurosurgery

Published: November 17, 2023

OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts.

OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts.

Journal: Human molecular genetics

Published: November 02, 2023

Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutation.

Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutation.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: December 23, 2022

Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts.

Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts.

Journal: Human molecular genetics

Published: June 10, 2022

A rare association of anti-alanine-transfer RNA synthetase (anti-PL12) syndrome and sporadic inclusion body myositis.

A rare association of anti-alanine-transfer RNA synthetase (anti-PL12) syndrome and sporadic inclusion body myositis.

Journal: Scandinavian journal of rheumatology

Published: August 07, 2017

An inflammatory myopathy unmasks a case of leprosy in an Italian patient.

An inflammatory myopathy unmasks a case of leprosy in an Italian patient.

Journal: Journal of neurology

Published: May 20, 2015

A rare case of multiple sclerosis and McArdle disease.

A rare case of multiple sclerosis and McArdle disease.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: February 11, 2015

Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis.

Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis.

Journal: Neuropathology and applied neurobiology

Published: October 06, 2012

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Last Updated: 09/26/2026