Supported by grants from NIH-NINDS (NS40593, NS057780, NS065027 to L Pozzo-Miller) and NIH-NICHD (U54 grant HD061222 and IDDRC grant HD38985 to AK Percy), the International Rett Syndrome Foundation, ...
One particular protein lies at the heart of brain development. A master regulator of gene expression, it’s abundantly present in neurons, and its dysfunction underlies Rett syndrome, a neurological ...
The neurodevelomental disease Rett syndrome is usually caused by mutations in a gene called MECP2, which is located on the X chromosome. Patients lose coordination, mobility, and their ability to ...
A new UC Davis MIND Institute study offers critical insights into Rett syndrome, a rare genetic condition that affects mostly girls. The research reveals how this condition affects males and females ...
Frank regression ensues with poor social contact and loss of communication and finger skills Stabilization during early school-age children with improved social contact, eye gaze and communication ...
Findings bolster the idea that the functions of this protein -- MeCP2 -- are more centered on nucleosomes, rather than other forms of DNA. One particular protein lies at the heart of brain development ...
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