Reference: 7NR1/1 Abstract: PROJECT DETAILS beginning: n.a end: n.a Country of research: Italy, US Counry of funding source: United States Funding organization: Bilateral Italy (ISS)ﾗUSA (NIH, Office for rare diseases) Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: 1F31MH078678n.a.1A2 Abstract: MeCP2 is a transcriptional repressor critical for normal neurological function. Rett syndrome (RTT) is a progressive neurodevelopmental disease caused by predominantly loss of function mutations in the X-linked gene encoding the transcriptional repressor, methyl-CpG-binding protein 2 (MECP2) genes. Classic RTT patients exhibit a spectrum of neurological phenotypes that include tremors, ataxia, seizures, … Read more
Reference: 5F31MH078678n.a.2 Abstract: MeCP2 is a transcriptional repressor critical for normal neurological function. Rett syndrome (RTT) is a progressive neurodevelopmental disease caused by predominantly loss of function mutations in the X-linked gene encoding the transcriptional repressor, methyl-CpG-binding protein 2 (MECP2) genes. Classic RTT patients exhibit a spectrum of neurological phenotypes that include tremors, ataxia, seizures, … Read more
Reference: ISS-NIH 5301/530H Abstract: PROJECT DETAILS beginning: n.a end: n.a Country of research: Italy, US Counry of funding source: United States Funding organization: Bilateral Italy (ISS)ﾗUSA (NIH, Office for rare diseases) Financing: NATIONAL FUNDINGS – 0 € hyperlink
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