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Molecular and cellular mechanism modulating GBA mutation penetrance in Parkinson’s disease

Project
Il progetto ha come obiettivo quello di identificare quali siano le cause che portano all’insorgenza di degenerazione dei neuroni dopaminergici a seguito di mutazioni in eterozigosi a carico del gene GBA. Questi studi verranno condotti su modelli di organoide midbrain.
  • Overview
  • Research Areas
  • Publications

Overview

Contributors

AURELI MASSIMO   Scientific Manager  

Departments involved

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale   Principale  

Type

PRIN2017 - PRIN bando 2017

Funder

MINISTERO DELL'ISTRUZIONE E DEL MERITO
External Organization Funding Organization

Date/time interval

September 17, 2019 - September 16, 2022

Project duration

36 months

Research Areas

Concepts


Settore BIO/10 - Biochimica

Publications

Outputs (4)

α-Synuclein Oligomers in Skin Biopsies Predict the Worsening of Cognitive Functions in Parkinson’s Disease: A Single-Center Longitudinal Cohort Study 
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
MULTIDISCIPLINARY DIGITAL PUBLISHING INSTITUTE (MDPI)
2024
Academic Article
Open Access
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Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 
MOVEMENT DISORDERS
WILEY BLACKWELL PUBLISHING
2022
Academic Article
Open Access
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β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 
CELLS
MDPI
2022
Academic Article
Open Access
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Screening of LRP10 mutations in Parkinson's disease patients from Italy 
PARKINSONISM & RELATED DISORDERS
ELSEVIER
2021
Academic Article
Reserved Access
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