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NeuronAgeScreen SIGNED

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

Total Cost €

0

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.

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

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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