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Pathogenic mechanisms of HSPB8 mutations in neuromuscular diseases: the role of the ribosomal and protein quality control system and the integrated stress response - I annualità

Project
  • Academic Signature
  • Overview
  • Research Areas
  • Publications

Academic Signature

Il servizio di classificazione ACADEMIC SIGNATURE è IN BETA TESTING e i risultati potrebbero non essere corretti

Academic Signature (3)

Mutation
Genetic Variation
Neuromuscular Diseases
Nervous System Diseases
Integrated Stress Response
Stress, Physiological

Overview

Contributors

POLETTI ANGELO   Scientific Manager  

Departments involved

Dipartimento di Scienze Farmacologiche e Biomolecolari Rodolfo Paoletti   Principale  

Type

INTLI - Finanziamenti internazionali

Funder

AFM-TELETHON - ASS. FRANCAISE CONTRE LES MYOPATHIES
External Organization Funding Organization

Date/time interval

January 1, 2026 - December 31, 2026

Project duration

12 months

Research Areas

Concepts


Settore BIOS-10/A - Biologia cellulare e applicata

Publications

Outputs

Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations 
BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE
ELSEVIER
2026
Academic Article
Partially Open Access
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