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NeuroRBP SIGNED

Studying RNA-binding proteins involved in neural differentiation and degeneration

Total Cost €

EC-Contrib. €

Partnership

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NeuroRBP project word cloud

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

risk proteins ipsc diseases machine discover rate nuclear integrate stability data stem malfunction localization degeneration neurodegenerative severe differentiation rnas rbps binding transcription export amyotrophic detecting learning immediately pluripotent tremor lateral neurodegeneration assays post track coordinate sclerosis light underscored output translation regulation shed transcriptional identification als ataxia mechanism rna mutations treat patient therapeutic individuals neural model cells

Project "NeuroRBP" data sheet

The following table provides information about the project.

Coordinator	THE FRANCIS CRICK INSTITUTE LIMITED Organization address address: 1 MIDLAND ROAD city: LONDON postcode: NW1 1AT website: www.crick.ac.uk 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	United Kingdom [UK]
Total cost	195˙454 €
EC max contribution	195˙454 € (100%)
Programme	1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
Code Call	H2020-MSCA-IF-2017
Funding Scheme	MSCA-IF-EF-ST
Starting year	2019
Duration (year-month-day)	from 2019-06-01 to 2021-05-31

Partnership

Take a look of project's partnership.

#	participants	country	role	EC contrib. [€]
1	THE FRANCIS CRICK INSTITUTE LIMITED THE FRANCIS CRICK INSTITUTE LIMITED Organization address address: 1 MIDLAND ROAD city: LONDON postcode: NW1 1AT website: www.crick.ac.uk contact info title: n.a. name: n.a. surname: n.a. function: n.a. email: n.a. telephone: n.a. fax: n.a.	UK (LONDON)	coordinator	195˙454.00

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Project objective

RNA-binding proteins (RBPs) coordinate post-transcriptional regulation immediately after transcription by RNA-processing, nuclear export, localization, stability and translation rate of RNAs. The importance of these RBPs in neural development have been underscored by detecting their mutations in severe neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), ataxia or tremor. In this project, using the assays that I developed specifically for the identification of RBPs I want to track down novel RBPs involved in neural differentiation. I will use patient-derived induced pluripotent stem cells (iPSC), as model system to discover RBPs that their malfunction may lead to neurodegeneration. Furthermore, I will identify the binding targets of the RBPs to determine the pathways that are affected. Finally, using machine-learning methods I will integrate these data to shed new light on the mechanism of neural differentiation and degeneration. The output of this project in long term will help to identify individuals at risk, and to develop better therapeutic approaches to treat neurodegenerative diseases.

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The information about "NEURORBP" are provided by the European Opendata Portal: CORDIS opendata.