Opendata, web and dolomites

ACE-OF-SPACE SIGNED

Analysis, control, and engineering of spatiotemporal pattern formation

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ACE-OF-SPACE project word cloud

Explore the words cloud of the ACE-OF-SPACE project. It provides you a very rough idea of what is the project "ACE-OF-SPACE" about.

stability    imaging    differentiate    embryos    talk    underlying    bacterial    sources    break    mysterious    vertebrate    optogenetics    extra    maternal    nodal    previously    mammalian    members    unclear    independent    time    patterns    orchestrate    self    absence    mediated    patterning    temporally    regulated    tissues    tgf    identical    diffusion    biophysical    signals    initially    beta    asymmetric    allocation    questions    synthetic    organizing    sufficient    experimentally    arise    engineer    organ    tissue    organize    axis    adult    signaling    prior    asymmetries    suggest    cell    population    engineering    small    gain    insights    cells    indicates    space    zebrafish    analyze    reaction    form    biology    patterned    mechanism    molecules    pattern    first    embryogenesis    axes    developmental    begun    demonstrated    opens    superfamily    modeling    precursors    stem    minimal    central    mouse    quantitative    unknown    theoretical    plan    understand    embryonic    mathematical    cross    systems    secondary    risk    signal    body    symmetry    strategies    colonies    thought    bmp    combination    opposing    interact    mechanisms    homogeneous   

Project "ACE-OF-SPACE" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

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 1˙997˙750 €
 EC max contribution 1˙997˙750 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-07-01   to  2025-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 1˙997˙750.00

Map

 Project objective

A central problem in developmental biology is to understand how tissues are patterned in time and space - how do identical cells differentiate to form the adult body plan? Patterns often arise from prior asymmetries in developing embryos, but there is also increasing evidence for self-organizing mechanisms that can break the symmetry of an initially homogeneous cell population. These patterning processes are mediated by a small number of signaling molecules, including the TGF-β superfamily members BMP and Nodal. While we have begun to analyze how biophysical properties such as signal diffusion and stability contribute to axis formation and tissue allocation during vertebrate embryogenesis, three key questions remain. First, how does signaling cross-talk control robust patterning in developing tissues? Opposing sources of Nodal and BMP are sufficient to produce secondary zebrafish axes, but it is unclear how the signals interact to orchestrate this mysterious process. Second, how do signaling systems self-organize to pattern tissues in the absence of prior asymmetries? Recent evidence indicates that axis formation in mammalian embryos is independent of maternal and extra-embryonic tissues, but the mechanism underlying this self-organized patterning is unknown. Third, what are the minimal requirements to engineer synthetic self-organizing systems? Our theoretical analyses suggest that self-organizing reaction-diffusion systems are more common and robust than previously thought, but this has so far not been experimentally demonstrated. We will address these questions in zebrafish embryos, mouse embryonic stem cells, and bacterial colonies using a combination of quantitative imaging, optogenetics, mathematical modeling, and synthetic biology. In addition to providing insights into signaling and development, this high-risk/high-gain approach opens exciting new strategies for tissue engineering by providing asymmetric or temporally regulated signaling in organ precursors.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "ACE-OF-SPACE" 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 "ACE-OF-SPACE" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

HYDROGEN (2019)

HighlY performing proton exchange membrane water electrolysers with reinforceD membRanes fOr efficient hydrogen GENeration

Read More  

E-DIRECT (2020)

Evolution of Direct Reciprocity in Complex Environments

Read More  

REPLAY_DMN (2019)

A theory of global memory systems

Read More