MACE

Maternal Communication with embryo

 Coordinatore THE UNIVERSITY OF SHEFFIELD 

 Organization address address: FIRTH COURT WESTERN BANK
city: SHEFFIELD
postcode: S10 2TN

contact info
Titolo: Dr.
Nome: Justine
Cognome: Daniels
Email: send email
Telefono: +44 0114 2221455
Fax: +44 0 114 2221455

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 172˙434 €
 EC contributo 172˙434 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-09-01   -   2012-08-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF SHEFFIELD

 Organization address address: FIRTH COURT WESTERN BANK
city: SHEFFIELD
postcode: S10 2TN

contact info
Titolo: Dr.
Nome: Justine
Cognome: Daniels
Email: send email
Telefono: +44 0114 2221455
Fax: +44 0 114 2221455

UK (SHEFFIELD) coordinator 172˙434.64

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 Word cloud

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environment    interaction    studied    temporal    embryo    oviduct    model    fertility    interactome    silico    communication    health    human    embryos    proteomic    livestock    maternal    biological    horn    uterine    systematic   

 Obiettivo del progetto (Objective)

'Mechanisms of interactions of embryos with their maternal environment are important biological filters limiting reproductive success, both in livestock and the human. Although several aspects of the embryo-maternal interactome have been studied, there is so far no systematic analysis of this biological module. Increasing our knowledge regarding maternal interaction with embryos will lead to creation of novel molecular markers of fertility that will help to improve the fertility of livestock population by genomic selection and thus provide unique competitive advantages to the animal breeding industry. Knowledge of the embryo-maternal interactome will facilitate novel approaches for improving the efficiency and safety of assisted reproduction techniques. Finally, this knowledge has cross-disciplinary applications in human health and is of immense importance for future public health. No systematic studies to date have been performed to allow construction of an in-silico model for the temporal sequence of events involved in maternal communication with embryos. All investigations so far have studied this interaction in isolation, without consideration of spatial or temporal components that may confer consequences for developmental potential. Early embryonic development, implantation and maintenance of pregnancy are critically dependent for intact and efficient communication between embryo and the maternal tract. The overall objective of this application is to identify the local proteomic factors produced in porcine oviduct and uterine horn in response to developing embryo. This information will be used to construct a systemic in-silico based model of oviduct and uterine horn proteomic secretome environment and changes in this milieu, due to embryo development. For this purpose, we evaluate the oviduct secretory proteomic profile alteration in response to embryos at different stage of development.'

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