Rett syndrome is a severe pediatric neurological disorder caused by loss of function mutations within the gene encoding methyl CpG-binding protein 2 (MeCP2). Although MeCP2 is expressed near ubiquitously, the primary pathophysiology of Rett syndrome stems from impairments of nervous system function. One alteration within different regions of the MeCP2-deficient brain is the presence of hyper-excitable network responses. In the hippocampus, such responses exist despite there being an overall decrease in spontaneous excitatory drive within the network. In this study, we generated and used mathematical, neuronal network models to resolve this apparent paradox. We did this by taking advantage of previous mathematical modelling insights that ind...
Rett Syndrome (RTT) is a developmental disorder that affects numerous neuronal systems that underlie...
Rett syndrome, an autism spectrum disorder with prominent motor and cognitive features, results from...
Abstract Background Rett syndrome (RTT) is a neurodev...
Rett syndrome (RTT) is a disorder with a pronounced neurological phenotype and is caused mainly by m...
Intractable epilepsy remains one of the top issues affecting the quality of living in Rett children....
Mutations in MECP2 cause Rett syndrome and some related forms of mental retardation and autism. Mecp...
Excess glutamate during intense neuronal activity is not instantly cleared and may accumulate in the...
Rett syndrome (RTT) arises from loss-of-function mutations in methyl-CpG binding protein 2 gene (Mec...
Mutations of MECP2 cause Rett syndrome (RTT), a neurodevelopmental disorder leading to loss of motor...
Many postnatal onset neurological disorders such as autism spectrum disorders (ASDs) and intellectua...
Excess glutamate during intense neuronal activity is not instantly cleared and may accumulate in the...
Rett syndrome (RTT) is an X-linked neurological disorder which is caused by sporadic mutations in th...
Abstract MECP2 mutations cause Rett syndrome (RTT), a severe and progressive neurodevelopmental diso...
<p>Correction: Network Models Predict that Reduced Excitatory Fluctuations Can Give Rise to Hippocam...
Rett syndrome (RTT) is a severe neurodevelopmental disorder primarily caused by heterozygous loss-of...
Rett Syndrome (RTT) is a developmental disorder that affects numerous neuronal systems that underlie...
Rett syndrome, an autism spectrum disorder with prominent motor and cognitive features, results from...
Abstract Background Rett syndrome (RTT) is a neurodev...
Rett syndrome (RTT) is a disorder with a pronounced neurological phenotype and is caused mainly by m...
Intractable epilepsy remains one of the top issues affecting the quality of living in Rett children....
Mutations in MECP2 cause Rett syndrome and some related forms of mental retardation and autism. Mecp...
Excess glutamate during intense neuronal activity is not instantly cleared and may accumulate in the...
Rett syndrome (RTT) arises from loss-of-function mutations in methyl-CpG binding protein 2 gene (Mec...
Mutations of MECP2 cause Rett syndrome (RTT), a neurodevelopmental disorder leading to loss of motor...
Many postnatal onset neurological disorders such as autism spectrum disorders (ASDs) and intellectua...
Excess glutamate during intense neuronal activity is not instantly cleared and may accumulate in the...
Rett syndrome (RTT) is an X-linked neurological disorder which is caused by sporadic mutations in th...
Abstract MECP2 mutations cause Rett syndrome (RTT), a severe and progressive neurodevelopmental diso...
<p>Correction: Network Models Predict that Reduced Excitatory Fluctuations Can Give Rise to Hippocam...
Rett syndrome (RTT) is a severe neurodevelopmental disorder primarily caused by heterozygous loss-of...
Rett Syndrome (RTT) is a developmental disorder that affects numerous neuronal systems that underlie...
Rett syndrome, an autism spectrum disorder with prominent motor and cognitive features, results from...
Abstract Background Rett syndrome (RTT) is a neurodev...