Characterization of novel proteins influencing MeCP2 activity and analysis of their possible involvement in Rett Syndrome

Reference: Charlotte Kilstrup-Nielsen Abstract: n.a PROJECT DETAILS  beginning: 2004. end: 2006. Country of research: Italy Counry of funding source: United States Funding organization: Research Sponsor: Robert C. & Adele R. Schiff Foundation Financing: PRIVATE FUNDERS – 59 120 € hyperlink

Molecular pathologies and functional interactions of the X-linked MECP2 and CDKL5 genes

Reference: Charlotte Kilstrup-Nielsen Abstract: Rett syndrome (RTT) is a severe pediatric neurological disorder that, because of its incidence, represents the most common genetic cause of severe intellectual disability in girls worldwide. Several RTT variants have been described ranging from milder forms with a later age of onset to conditions with very early severe epileptic manifestations. … Read more

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