Postnatal deficits in brain-derived neurotrophic factor (BDNF) are thought to contribute to
pathogenesis of Rett syndrome (RTT), a progressive neurodevelopmental disorder caused …

Rett syndrome (RTT) is caused by loss-of-function mutations in the gene encoding methyl-
CpG-binding protein 2 (MeCP2). Although MeCP2 is thought to act as a transcriptional …

Disruptions in brain-derived neurotrophic factor (BDNF) expression are proposed to
contribute to the molecular pathogenesis of Rett syndrome (RTT), a severe neurological …

Dysfunction of the neurotrophin brain-derived neurotrophic factor (BDNF) is implicated in
Rett syndrome (RTT), but the state of its releasable pool and downstream signaling in mice …

Reduced levels of brain-derived neurotrophic factor (BDNF) are thought to contribute to the
pathophysiology of Rett syndrome (RTT), a severe neurodevelopmental disorder caused by …

Rett syndrome (RTT) is a devastating neurodevelopmental disorder with autistic features
caused by loss-of-function mutations in the gene encoding methyl-CpG-binding protein 2 …

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) …

Mutations in the MECP2 gene cause the neurodevelopmental disorder Rett syndrome
(RTT). Previous studies have shown that altered MeCP2 levels result in aberrant neurite …

Rett syndrome (RTT) results from loss-of-function mutations in the gene encoding the methyl-
CpG-binding protein 2 (MeCP2) and is characterized by abnormal motor, respiratory and …

Mutations in the MECP2 gene cause Rett syndrome (RTT). Bdnf is a MeCP2 target gene;
however, its role in RTT pathogenesis is unknown. We examined Bdnf conditional mutant …