The Ups and Downs of BDNF in Rett Syndrome

نویسندگان

  • Yi E. Sun
  • Hao Wu
چکیده

Rett syndrome (RTT) is an X-linked postnatal neurodevelopmental disorder, which is primarily caused by mutations in the gene encoding methyl-CpG binding protein 2 (MeCP2). A number of MeCP2 target genes have been identified, including the neurotrophic factor BDNF; however, the functional relevance of these targets has not been established. In this issue of Neuron, Chang et al. provide the first in vivo evidence for a functional interaction between BDNF and MeCP2.

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عنوان ژورنال:
  • Neuron

دوره 49  شماره 

صفحات  -

تاریخ انتشار 2006