Reference: 301/01/P068 Abstract: ProjektGA CR 301/01/P068 focused on molecular-biological analysis MeCP2genu. Its defect leads to clinical manifestations of Rett syndrome (RS) (OMIM312750), which is the second most common cause of mental retardation dívek.Dědičnost RS gonosomal dominant with incidence approximately 1 to 000 10000-15; vast majority of mutations created de novo. MECP2 gene, described in 1999, … Read more
Reference: R01 NS047584n.a.1- Tupler, Rossella Abstract: n.a PROJECT DETAILS beginning: 2003. end: 2008. Country of research: Italy Counry of funding source: United States Funding organization: National Institutes of Health; US Financing: NATIONAL FUNDINGS – 853 913 € hyperlink
Reference: 2003-742 Abstract: n.a PROJECT DETAILS beginning: 2002. end: 2003. Country of research: Sweden Counry of funding source: Sweden Funding organization: Swedish Research Council Financing: NATIONAL FUNDINGS – 300 000 € hyperlink
Reference: B2 – Subproject to SFB 545: Molecular mechanisms of genetic diseases Abstract: PROJECT DETAILS beginning: 1997. end: 2003. Country of research: Germany Counry of funding source: Germany Funding organization: GermanﾠResearch Foundation Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: QLK2-CT-2002-51761 Abstract: Ret Syndrome, an important cause of mental retardation in women, is associated with mutations in the gene encoding methyl- Cog binding protein. The aim of this project is to identify target genes whose expression is altered as a result of Mapco mutations. PROJECT DETAILS beginning: 2003. end: 2005. Country of research: Spain … Read more
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