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Content archived on 2024-05-24

Understanding the chronic neurological alterations of down syndrome and their associated phenotypes and development of molecular targets for their correction (T21 TARGETS)

Objective

Despite a vast amount of investigation on the pathophysiology of Down syndrome (DS) (T21), the molecular, biochemical and cellular bases of this common cause of mental retardation (over 500.000 cases in Europe) are still unknown. The sequence of human chromosome 21, cells and tissues from individuals with partial or regular T21 (molecularly and phenotypically described) and functional approaches (expression profiling, yeast double hybrid, transcriptome and proteome) should permit: a/to identify the molecules that are involved in DS brain alterations and the modifier factors responsible of the phenotypic variability; b/to modelize the dosage effects of the DS transcriptome in mouse; and c/ to develop protective and therapeutic strategies for the treatment of the chronic neurological alterations of DS patients. This understanding of DS should also provide basic knowledge about the causes of common clinical neurological alterations in humans.

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Call for proposal

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Coordinator

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
EU contribution
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Address
Case 7104 - Place Jussieu 2
75251 PARIS
France

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Total cost
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Participants (7)