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 TERMINÉ 

Proof of Concept study for ERC NIPD discovered biomarkers (mR-NIPD)

Date du début: 1 déc. 2016, Date de fin: 31 mai 2018,

... at risk of chromosomal abnormalities such as, but not limited to, Down syndrome (trisomy 21), Patau syndrome (trisomy 13) and Edward’s syndrome (trisomy 18). In this ERC Proof of Concept Grant (mR-NIPD), we anticipate to correlate already discovered DNA biomarkers of the ERC NIPD (funded ERC) with biomarkers in mRNA transcripts. The method, directly related to the currently funded ERC, will use m ...
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 1

 TERMINÉ 

A Novel Non-Invasive Prenatal Diagnosis for Genetic Disorders (NIPD)

Date du début: 1 mai 2013, Date de fin: 30 avr. 2018,

Non-Invasive Prenatal Diagnosis (NIPD) has been one of the most fascinating research fields during the last decade. The identification of small amounts of fetal DNA in maternal circulation has opened new possibilities for NIPD. Up until today, two methods have achieved accurate and validated NIPD methods for trisomy 21. The first NIPD for trisomy 21 was based on next generation sequencing and the ...
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 2

 TERMINÉ 

A New GEnetic LABoratory for non-invasive prenatal diagnosis (ANGELab)

Date du début: 1 oct. 2012, Date de fin: 31 mars 2017,

This project will develop a family of In-Vitro Diagnostic Systems that will transfer for the first time novel Non Invasive Prenatal Diagnostic (NIPD) methods in tube to a LabonaChip format. This family will consist of three research systems chosen to cover all prenatal diagnosis models:- ANGELAB1. This system will use a LabonaChip to extract fetal DNA from the mother´s plasma based on differences ...
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