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The journal of neuroscience : the official journal of the Society for Neuroscience.

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The article was published on 1981-01-01 and is currently open access. It has received 1737 citations till now.

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

F. Kyle Satterstrom, +201 more
- 06 Feb 2020 - 
TL;DR: The largest exome sequencing study of autism spectrum disorder (ASD) to date, using an enhanced analytical framework to integrate de novo and case-control rare variation, identifies 102 risk genes at a false discovery rate of 0.1 or less, consistent with multiple paths to an excitatory-inhibitory imbalance underlying ASD.
Journal ArticleDOI

The Transcription Factor TFEB Links mTORC1 Signaling to Transcriptional Control of Lysosome Homeostasis

TL;DR: TFEB is identified as a target of mTOR and a mechanism for matching the transcriptional regulation of genes encoding proteins of autophagosomes and lysosomes to cellular need is suggested.
References
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Effects of Neural Morphology and Input Distribution on Synaptic Processing by Global and Focal NMDA-Spikes.

TL;DR: It is shown that the input resistance (RIN) plays a major role in influencing spike initiation; while the classical, focal NMDA-spike depended upon the local (dendritic) RIN, the threshold of global NMDA -spike generation was set by the somatic RIN.
Journal ArticleDOI

Silencing of Cholinergic Basal Forebrain Neurons Using Archaerhodopsin Prolongs Slow-Wave Sleep in Mice

TL;DR: The results indicate that the main effect of these neurons is to terminate SWS, whereas wakefulness or REM sleep may be determined by co-operation of the cholinergic BF neurons with other arousal-sleep control systems.
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Basal forebrain somatostatin cells differentially regulate local gamma oscillations and functionally segregate motor and cognitive circuits

TL;DR: Optogenetic stimulation and in vivo recordings of transgenic mice are used to show that somatostatin neurons exert an anatomically specialized role in the coordination of subcortical gamma oscillations of the rostral basal forebrain, which further supports the role of the basal fore brain as a subCortical switch commanding transitions between internally and externally oriented brain states.
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Hippocampal neurophysiology is modified by a disease-associated C-terminal fragment of tau protein.

TL;DR: A transgenic mouse that selectively accumulates a C-Terminal 35 kDa human tau fragment (Tau35) results in a significant increase of short-term facilitation of the synaptic response in the theta frequency range (10 Hz), without affecting basal synaptic transmission and long-term synaptic plasticity.