Epithelia delimits glial apical polarity against mechanical shear to maintain glia-neuron architecture.
Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder.
Perception and adaptation of receptive prosody in autistic adolescents.
Microexons: At the nexus of nervous system development, behaviour and autism spectrum disorder.
Continuous whole-body 3D kinematic recordings across the rodent behavioral repertoire.
Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice.
Loss of UBE3A from TH-expressing neurons suppresses GABA co-release and enhances VTA-NAc optical self-stimulation.
Subcellular organization of UBE3A in neurons.
Persistent neuronal UBE3A expression in the suprachiasmatic nucleus of Angelman syndrome model mice.
GABAergic neuron-specific loss of UBE3A causes Angelman syndrome-like EEG abnormalities and enhances seizure susceptibility.
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