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NeuronAgeScreen SIGNED

A Drug Discovery and Target Identification Screening Platform for Age-Associated Neurodegenerative Disorders

Total Cost €

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EC-Contrib. €

0

Partnership

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 NeuronAgeScreen project word cloud

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

model    521    ipr    parkinson    identification    neurodegenerative    maladies    stage    streamlining    precisely    conserved    uniquely    life    platform    facets    imaging    human    combines    stroke    organism    attractive    diseases    discovery    neurons    dependability    malleable    organisms    490    linked    manifested    genetic    readily    alzheimer    nervous    compound    neuronage    pervasive    nematode    dementia    context    vivo    neurodegeneration    offers    societal    intimately    universally    devising    ataxias    dissected    platforms    drug    demonstration    efficient    battling    billion    therapeutic    decrease    erc    neuronal    marked    213    experimental    screening    ageing    betterment    interventions    nature    protection    global    susceptibility    525    throughput    combating    genes    health    course    evolutionary    pressing    function    innovation    enterprise    devastating    pathologies    elegans    strategies    convenient    intervention    technologies    prowess    quality    manipulation    disease    patent    prevalence    innovative    disorders    microfluidics    overarching    commercialization    chemical    types    file    versatile    populations   

Project "NeuronAgeScreen" data sheet

The following table provides information about the project.

Coordinator
IDRYMA TECHNOLOGIAS KAI EREVNAS 

Organization address
address: N PLASTIRA STR 100
city: IRAKLEIO
postcode: 70013
website: www.forth.gr

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 Greece [EL]
 Total cost 150˙000 €
 EC max contribution 150˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-PoC
 Funding Scheme ERC-POC
 Starting year 2017
 Duration (year-month-day) from 2017-05-01   to  2018-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IDRYMA TECHNOLOGIAS KAI EREVNAS EL (IRAKLEIO) coordinator 150˙000.00

Map

 Project objective

Battling human neurodegenerative pathologies, and their pervasive societal impact, is a global multi-billion Euro enterprise. Ageing is universally associated with marked decrease of neuronal function and higher susceptibility to neurodegeneration. In human populations, this is manifested as an ever-increasing prevalence of devastating neurodegenerative conditions, including Alzheimer’s and Parkinson’s disease, stroke, several ataxias, and other types of dementia. Development of therapeutic interventions against such maladies is becoming a pressing priority. Drug discovery and drug target identification are two intimately linked facets of intervention strategies aimed at effectively combating human disorders. Genes linked to human diseases often function in evolutionary conserved pathways, readily dissected in simple model organisms. Such organisms provide attractive platforms for devising and streamlining efficient drug discovery and target identification methodologies. During the course of the ERC project NeuronAge, we developed a convenient and versatile platform for high-throughput chemical compound screening based on the nematode C. elegans (Nature 521: 525; Nature 490: 213). This innovative platform uniquely combines state-of-the-art microfluidics technologies for imaging and manipulation of neurons in vivo, with the experimental prowess of C. elegans, a highly malleable genetic model, which offers a precisely defined nervous system, two features that are not available in any other organism. We propose to: (1) bring this high-throughput compound screening system to pre-demonstration stage; (2) evaluate its dependability for drug target identification and drug discovery; (3) file US and European patent applications for IPR protection; and (4) identify potential commercialization opportunities. The overarching aim is to facilitate the exploitation of the innovation generated in the context of NeuronAge towards the betterment of human health and quality of life.

 Publications

year authors and title journal last update
List of publications.
2018 Athanasios Metaxakis, Dionysia Petratou, Nektarios Tavernarakis
Multimodal sensory processing in Caenorhabditis elegans
published pages: 180049, ISSN: 2046-2441, DOI: 10.1098/rsob.180049
Open Biology 8/6 2019-05-23
2018 Athanasios Metaxakis, Christina Ploumi, Nektarios Tavernarakis
Autophagy in Age-Associated Neurodegeneration
published pages: 37, ISSN: 2073-4409, DOI: 10.3390/cells7050037
Cells 7/5 2019-05-23
2018 Ioanna Daskalaki, Ilias Gkikas, Nektarios Tavernarakis
Hypoxia and Selective Autophagy in Cancer Development and Therapy
published pages: , ISSN: 2296-634X, DOI: 10.3389/fcell.2018.00104
Frontiers in Cell and Developmental Biology 6 2019-05-23
2018 Vassiliki Nikoletopoulou, Nektarios Tavernarakis
Regulation and Roles of Autophagy at Synapses
published pages: 646-661, ISSN: 0962-8924, DOI: 10.1016/j.tcb.2018.03.006
Trends in Cell Biology 28/8 2019-05-23
2018 Ilias Gkikas, Konstantinos Palikaras, Nektarios Tavernarakis
The Role of Mitophagy in Innate Immunity
published pages: , ISSN: 1664-3224, DOI: 10.3389/fimmu.2018.01283
Frontiers in Immunology 9 2019-05-23
2018 Nikos Kourtis, Nektarios Tavernarakis
Small heat shock proteins and neurodegeneration: recent developments
published pages: 94-102, ISSN: 1868-5021, DOI: 10.1515/bmc-2018-0009
Biomolecular Concepts 9/1 2019-05-23
2018 Matthias Rieckher, Maria Markaki, Andrea Princz, Björn Schumacher, Nektarios Tavernarakis
Maintenance of Proteostasis by P Body-Mediated Regulation of eIF4E Availability during Aging in Caenorhabditis elegans
published pages: 199-211.e6, ISSN: 2211-1247, DOI: 10.1016/j.celrep.2018.09.009
Cell Reports 25/1 2019-05-23

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