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Content archived on 2024-05-27

Peroxisomal diseases: elucidation of the pathogenesis and evaluation of treatments by using mouse models (MMPD)

Objective

The peroxisomal disorders represent a newly recognised group of rare, inherited metabolic diseases with diverse perturbations of lipid metabolism. Although much has been learned about the enzymatic and genetic basis of these disorders, there is little information with respect to the pathogenetic mechanisms. It is our purpose to generate and analyse mouse models mimicking these diseases (MPF-2 deficiency, Refsum disease, RCDP type 1 and 2). Specific aims are:
1) to make an inventory of all metabolic changes in the different mouse models,
2) to investigate the onset and progression of pathologies in the different organs in particular in the central nervous system and in the neuromuscular system
3) to study the molecular mechanisms linking metabolic alterations with organ dysfunction by in vivo and in vitro approaches
4) to use these mouse models to evaluate diets and treatments.

Fields of science (EuroSciVoc)

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Topic(s)

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Call for proposal

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Funding Scheme

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Coordinator

KATHOLIEKE UNIVERSITEIT LEUVEN
EU contribution
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Address
Herestraat 49
3000 LOUVAIN / LEUVEN
Belgium

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Total cost

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Participants (3)

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