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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
Academic field
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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