Barbara Tedesco

Milan, Italy

Last Updated: 09/26/2026

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Found 39 publications

Chaperone-assisted selective autophagy (CASA) in polyglutamine-related diseases: From mechanisms to therapeutic perspectives.

Chaperone-assisted selective autophagy (CASA) in polyglutamine-related diseases: From mechanisms to therapeutic perspectives.

Journal: Journal of Huntington's disease

Published: September 03, 2026

Characterization of the frameshift c.515dupC knock-in mouse model of HSPB8-associated myopathy (MFM13) and evaluation of Trehalose as autophagy-modulating therapy.

Characterization of the frameshift c.515dupC knock-in mouse model of HSPB8-associated myopathy (MFM13) and evaluation of Trehalose as autophagy-modulating therapy.

Journal: bioRxiv : the preprint server for biology

Published: August 20, 2026

Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations.

Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: December 17, 2025

The alternative androgen receptor isoform A mitigates toxicity of polyglutamine-elongated mutant androgen receptor in spinal and bulbar muscular atrophy.

The alternative androgen receptor isoform A mitigates toxicity of polyglutamine-elongated mutant androgen receptor in spinal and bulbar muscular atrophy.

Journal: Journal of advanced research

Published: July 23, 2025

VCP modulation ameliorates pathological features in C9orf72 models.

VCP modulation ameliorates pathological features in C9orf72 models.

Journal: Cell death & disease

Published: May 24, 2025

Impairment of lysosomal quality control in Huntington disease.

Impairment of lysosomal quality control in Huntington disease.

Journal: Cell death & disease

Published: May 06, 2025

One gene, many phenotypes: the role of KIF5A in neurodegenerative and neurodevelopmental diseases.

One gene, many phenotypes: the role of KIF5A in neurodegenerative and neurodevelopmental diseases.

Journal: Cell communication and signaling : CCS

Published: April 18, 2025

FAK signaling pathways are modulated by HSPB8 and BAG3 in breast cancer.

FAK signaling pathways are modulated by HSPB8 and BAG3 in breast cancer.

Journal: Cell communication and signaling : CCS

Published: April 10, 2025

Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models.

Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models.

Journal: European journal of human genetics : EJHG

Published: January 22, 2025

Targeting androgen receptor stability and degradation: approaches for developing a therapy for spinal and bulbar muscular atrophy.

Targeting androgen receptor stability and degradation: approaches for developing a therapy for spinal and bulbar muscular atrophy.

Journal: Cell communication and signaling : CCS

Published: January 12, 2025

Small heat shock protein B8: from cell functions to its involvement in diseases and potential therapeutic applications.

Small heat shock protein B8: from cell functions to its involvement in diseases and potential therapeutic applications.

Journal: Neural regeneration research

Published: May 06, 2024

Lysosome quality control in health and neurodegenerative diseases.

Lysosome quality control in health and neurodegenerative diseases.

Journal: Cellular & molecular biology letters

Published: April 12, 2024

Showing 1-12 of 39

Last Updated: 09/26/2026