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TFZN SIGNED

Understanding the mechanisms that govern organ morphostasis and repair

Total Cost €

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EC-Contrib. €

0

Partnership

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Project "TFZN" data sheet

The following table provides information about the project.

Coordinator
HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH 

Organization address
address: INGOLSTADTER LANDSTRASSE 1
city: NEUHERBERG
postcode: 85764
website: www.helmholtz-muenchen.de

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 Germany [DE]
 Total cost 162˙806 €
 EC max contribution 162˙806 € (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-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-10-01   to  2021-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH DE (NEUHERBERG) coordinator 162˙806.00

Map

 Project objective

Neuromasts are the sensory organs used by fishes and amphibians to sense water displacement. Neuromasts contain hair cells that are very similar to our own inner ear cells. Unlike mammalian ear cells, bird and fish hair cells regenerate after ablated. Understanding the mechanisms responsible for the development and regeneration of the sensory organs holds the promise of treating deafness in humans. The study of neuromasts is also of advantage for basic science. With its three cell types, and 70 cells total, neuromasts are a relatively simple organ. They provide a good model to investigate unanswered questions about organogenesis: What makes cells proliferate during organ regeneration or development? What signals them to stop after normal organ size and cell number is reached? How is organ architecture – shape, cell placement, orientation– attained? Is it an intrinsic property of the interactions between its components (self-organization) or does it depend on external cues? I will establish a system for the production of neuromast organoids in vitro. This will serve to interrogate the role of self-organization in the process of tissue repair. I will also use a combination of single cell transcriptomics, fluorescence marker imaging, gene editing and pharmacological treatments to collect multidimensional data from cells during neuromast regeneration. The use of unbiased computational techniques derived from machine learning will help us untangle the molecular and cellular players driving cellular organization in this system.

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

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