24 posts found

Genetic strategies to repair brain circuits with altered MECP2

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The Rett syndrome (RTT) and the Autism Spectrum Disorder (ASD) are neurodevelopmental disorders which, although presenting different symptoms and evolution, are linked by a common factor: mutations in the same gene, called MECP2. But the answers on how and why the same gene could have a key role in the development of both diseases have […]

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The dynamic functional connectivity of the brain and the fMRI: an overview of analytical strategies

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Resting-state functional magnetic resonance imaging (fMRI) is a method of functional brain imaging (i.e., the measurement of the aspect of a brain area by images) that can be used to evaluate regional interactions that occur when a subject is resting. The fMRI has highlighted the rich structure of brain activity in absence of a task or stimulus. […]

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Central Serotonin Receptor 7 constitutes a potential therapeutic target for Rett Syndrome

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Rett syndrome is a neurodevelopment disorder affecting around 1 out of 10,000 girls, usually due to de novo mutations in the X-located gene MECP2. It is a complex disorder, both clinically and at a molecular level, and is typically characterized by a neurodevelopment regression starting at age 6 to 18 months after a normal early […]

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