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Synaptic Dysfunction in Alzheimer Disease

Project
Given an overwhelming increase of dementia costs and an aging population, there is an urgent need for finding novel therapies for Alzheimer Disease (AD). We are, however, facing a large number of failed clinical trials and a retraction of the nervous system R&D programmes from several big pharmaceutical companies. Increased collaboration between academia and the private sector is required to overcome this challenge.
The ¿Synaptic Dysfunction in Alzheimer Disease¿ (SyDAD) project will significantly contribute to this approach by training a new generation of researchers with experience and full understanding of the requirements of academia, pharmaceutical companies, the clinics and the society.
The research programme will focus on synaptic dysfunction, the main connection point between pathology and cognitive decline in AD. Given the complementary expertise, SyDAD will have excellent opportunities to delineate the cross-talk between different pathways underlying synaptic dysfunction in AD and to identify novel pharmaceutical targets. For future implementation of the research findings into clinical trials, a drug discovery platform will be elaborated, utilising the industrial and clinical expertise in the network.
The early-stage researchers (ESRs) will be trained in this environment and provided with a mind-set of future commercial and clinical utilisation of their research findings. Apart from the innovative and collaborative approach of the research programme, the ESRs will also be provided with a training programme where cutting-edge methodology, innovation and transferable skills are key components.
The trained ESRs will have excellent intersectoral and interdisciplinary career opportunities and will, together with the SyDAD partners, provide a solid ground to tackle one of the major societal challenges of our century: Finding therapies to decrease the suffering and economic burden of AD patients.
  • Overview
  • Publications

Overview

Contributors

DILUCA MONICA MARIA GRAZIA   Scientific Manager  

Departments involved

Dipartimento di Scienze Farmacologiche e Biomolecolari Rodolfo Paoletti   Principale  

Type

H20MCITNIF - Horizon 2020_Marie Skłodowska-Curie actions-Innovative Training Network (ITN)/Individual Fellowships (IF)

Funder

EUROPEAN COMMISSION
External Organization Funding Organization

Date/time interval

November 1, 2015 - October 31, 2019

Project duration

48 months

Publications

Outputs (4)

The development of ADAM10 endocytosis inhibitors for the treatment of Alzheimer's disease 
MOLECULAR THERAPY
CELL PRESS : ELSEVIER
2022
Academic Article
Open Access
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Cyclase-associated protein 2 dimerization regulates cofilin in synaptic plasticity and Alzheimer's disease 
BRAIN COMMUNICATIONS
OXFORD UNIVERSITY PRESS
2020
Academic Article
Open Access
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Loss of Ryanodine Receptor 2 impairs neuronal activity-dependent remodeling of dendritic spines and triggers compensatory neuronal hyperexcitability 
CELL DEATH AND DIFFERENTIATION
SPRINGER NATURE
2020
Academic Article
Open Access
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Amyloid-β oligomers regulate ADAM10 synaptic localization through aberrant plasticity phenomena 
MOLECULAR NEUROBIOLOGY
SPRINGER
2019
Academic Article
Open Access
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