Editorial Team

MECP2 PHOSPHORYLATION AND RELATED KINASES IN RETT SYNDROME

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Reference: RF-IRE-2008-1231829 Abstract: n.a PROJECT DETAILS  beginning: 2010. end: 2013. Country of research: Italy Counry of funding source: Italy Funding organization: Ministry of Health, Programma per la Ricerca Sanitaria 2008: attivit? di ricerca sulle Malattie Rare Financing: NATIONAL FUNDINGS – 230 769 € hyperlink

MeCP2 as a genome-wide modulator: the renewal of an old story.

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Reference: Abstract: Since the discovery of MeCP2, its functions have attracted the interest of generations of molecular biologists. Its function as a transducer of DNA methylation, the major post-biosynthetic modification found throughout genomes, and its association with the neurodevelopmental disease Rett syndrome highlight its central role as a transcriptional regulator, and, at the same time, … Read more

Joint project: European Rett Syndrome Network (EURORETT).ﾠShare TU Darmstadt.ﾠ

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Reference: 01GM0811 TIB Abstract: Although the biochemical function of the proteins involved in this disorder is known, the pathophysiological mechanisms are still mysterious, stressing the need for synergy and multidisciplinarity. Because Rett syndrome could be reversible, it is a priority to combine all possible approaches understand disease mechanisms. This could allow the rapid translation of … Read more

Induced pluripotent stem cells as in vitro models for the study of Rett syndrome pathogenesis and identification of therapeutic targets

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Reference: RF-TOS-2008-1225570 Abstract: n.a PROJECT DETAILS  beginning: 2010. end: 2013. Country of research: Italy Counry of funding source: Italy Funding organization: Ministry of Health, Programma per la Ricerca Sanitaria 2008: attivit? di ricerca sulle Malattie Rare Financing: NATIONAL FUNDINGS – 164 120 € hyperlink

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