Opendata, web and dolomites

DIVE into AD SIGNED

Study of tau strains to understand the phenotypic diversity of Alzheimer’s disease: A step toward personalized therapies

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 DIVE into AD project word cloud

Explore the words cloud of the DIVE into AD project. It provides you a very rough idea of what is the project "DIVE into AD" about.

citizens    societies    2050    ultimately    repertoire    diversity    discrete    patterns    cell    majority    correlates    sensitively    patient    prion    single    deposition    determinants    hallmark    clinical    shown    lines    metabolism    propagate    care    postulate    behaves    therapeutic    respective    millions    disease    strains    causative    therapies    generate    detect    deep    neuronal    biosensor    gender    template    spread    suffering    peptide    modifies    human    treat    technologies    pathophysiology    unsuccessfully    morphology    ad    tau    differences    19    rate    treatment    vast    event    variability    progression    neuron    patients    confirmed    modern    heterogeneity    samples    plan    variants    protein    vulnerability    responsible    neurodegeneration    innovative    cerebrospinal    conformation    conformers    biomarkers    course    pathology    accumulation    beta    expression    signatures    pathological    individual    aggregates    cognition    phenotypes    native    fidelity    optimize    fluid    brain    understand    ageing    potentially    alzheimer    dementia    seem   

Project "DIVE into AD" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITE DE GENEVE 

Organization address
address: RUE DU GENERAL DUFOUR 24
city: GENEVE
postcode: 1211
website: www.unige.ch

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Switzerland [CH]
 Total cost 278˙840 €
 EC max contribution 278˙840 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-GF
 Starting year 2020
 Duration (year-month-day) from 2020-08-01   to  2023-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITE DE GENEVE CH (GENEVE) coordinator 278˙840.00
2    THE GENERAL HOSPITAL CORPORATION US (BOSTON MA) partner 0.00

Map

 Project objective

Dementia represents a major challenge for our ageing societies. The number of citizens suffering from dementia in the EU is expected to reach 19 millions by 2050. Alzheimer’s disease (AD) is responsible for the vast majority of dementia cases. However there is still not a single available treatment that modifies the course of disease. Therefore, the development of innovative approaches to better understand the pathophysiology and ultimately treat patients must be a priority. This project aims to understand the determinants of the diversity of AD clinical phenotypes through the deep analysis of pathological variants of the tau protein. As the accumulation of Aβ peptide has long been considered a causative event in AD, most therapeutic approaches have targeted Aβ metabolism, but unsuccessfully. Modern biomarkers, have confirmed that the brain deposition of tau pathology, the other hallmark of AD, correlates much better with human cognition and neurodegeneration. Recently, it was shown that tau behaves like a prion and can spread from one neuron to another. Moreover, tau strains or conformers seem to template native tau and propagate the pathological conformation with high fidelity. Discrete tau strains generate distinct aggregates morphology or patterns of neuronal vulnerability. I postulate that different strains of tau are responsible for the variability of AD and may determine the progression rate, gender differences or clinical expression. Therefore, my objective is to develop the technologies to identify tau strains signatures in distinct AD phenotypes. In particular, I plan to develop and optimize biosensor cell lines that sensitively detect tau strains from human brain samples and cerebrospinal fluid, and characterize respective repertoire of tau strains. Understanding AD heterogeneity would potentially increase our ability to take care of every individual patient. In addition, this work could lead to the development of biomarkers and novel targeted therapies.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "DIVE INTO AD" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "DIVE INTO AD" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

EGeoCC (2019)

Ethnic geography and civil conflict

Read More  

ASSEMBLY (2019)

Advancing Synthethic Supramolecular chemical biology

Read More  

DEAP (2019)

Development of Epithelium Apical Polarity: Does the mechanical cell-cell adhesions play a role?

Read More