A leading theory holds that neurodevelopmental brain disorders arise from imbalances in excitatory and inhibitory (E/I) brain circuitry. However, it is unclear whether this one-dimensional model is rich enough to capture the multiple neural circuit alterations underlying brain disorders. Here, we combined computational simulations with analysis of in vivo two-photon Ca2+ imaging data from somatosensory cortex of Fmr1 knock-out (KO) mice, a model of Fragile-X Syndrome, to test the E/I imbalance theory. We found that: (1) The E/I imbalance model cannot account for joint alterations in the observed neural firing rates and correlations; (2) Neural circuit function is vastly more sensitive to changes in some cellular components over others; (3) ...
A typical symptom of epilepsy, a type of neurological disorder, includes a seizure caused by the sud...
Inhibitory interneurons are among the most diverse cell types in the brain; the hippocampus alone co...
Silencing of the Fmr1 gene causes fragile X syndrome. Although defects in synaptic plasticity in the...
A leading theory holds that neurodevelopmental brain disorders arise from imbalances in excitatory a...
Abnormal brain development manifests itself at different spatial scales. However, whether abnormalit...
In patients with Fragile X syndrome the fmr1 gene is silenced, leading to a lack of expression of th...
Subtle alterations in how cortical network dynamics are modulated by different behavioral states cou...
The Fragile X mental retardation protein (FMRP) is involved in many cellular processes and it regula...
Fragile X Syndrome (FXS), a common inheritable form of intellectual disability, is known to alter ne...
Fragile X Syndrome (FXS) is a neurodevelopmental disorder and the leading known genetic cause of aut...
Distinct genetic forms of autism are hypothesized to share a common increase in excitation inhibitio...
Background Excitation/inhibition (E/I) imbalance remains a widely discussed hypothesis in autism spe...
A common neurobiological mechanism in several neurodevelopmental disorders, including fragile X synd...
One prominent feature of brain computation is the excitation inhibition balance (E/I balance) that r...
Every second throughout life, cortical circuitry efficiently compresses and interprets huge volumes...
A typical symptom of epilepsy, a type of neurological disorder, includes a seizure caused by the sud...
Inhibitory interneurons are among the most diverse cell types in the brain; the hippocampus alone co...
Silencing of the Fmr1 gene causes fragile X syndrome. Although defects in synaptic plasticity in the...
A leading theory holds that neurodevelopmental brain disorders arise from imbalances in excitatory a...
Abnormal brain development manifests itself at different spatial scales. However, whether abnormalit...
In patients with Fragile X syndrome the fmr1 gene is silenced, leading to a lack of expression of th...
Subtle alterations in how cortical network dynamics are modulated by different behavioral states cou...
The Fragile X mental retardation protein (FMRP) is involved in many cellular processes and it regula...
Fragile X Syndrome (FXS), a common inheritable form of intellectual disability, is known to alter ne...
Fragile X Syndrome (FXS) is a neurodevelopmental disorder and the leading known genetic cause of aut...
Distinct genetic forms of autism are hypothesized to share a common increase in excitation inhibitio...
Background Excitation/inhibition (E/I) imbalance remains a widely discussed hypothesis in autism spe...
A common neurobiological mechanism in several neurodevelopmental disorders, including fragile X synd...
One prominent feature of brain computation is the excitation inhibition balance (E/I balance) that r...
Every second throughout life, cortical circuitry efficiently compresses and interprets huge volumes...
A typical symptom of epilepsy, a type of neurological disorder, includes a seizure caused by the sud...
Inhibitory interneurons are among the most diverse cell types in the brain; the hippocampus alone co...
Silencing of the Fmr1 gene causes fragile X syndrome. Although defects in synaptic plasticity in the...