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Opposing mechanisms determine dendrite arbor size during a critical period in Drosophila.

Without ribosome recycling factor, ribosomes in Escherichia coli accumulate in 3'-UTRs and queue upstream of stop codons, but no effects were observed on the translational coupling of neighboring genes.

Accumulation of perineuronal nets around parvalbumin (PV)-positive inhibitory interneurons closes visual cortical plasticity by selectively down-regulating thalamic synapses onto PV cells in a sensory-dependent manner.

Structural brain plasticity is encoded in the topographic distribution of Toll receptors and their ability to switch between alternative signalling outcomes, thus translating diverse sensory experience into structural change.

Critical networks show maximum pre-stimulus phase and amplitude regulation of stimulus-evoked responses.

Basal ganglia gene coexpression patterns shift across the sensorimotor critical period for vocal learning.

Mitochondria reach stable positions in dendrites during a critical developmental period of high motility.

The binocular matching of thalamic inputs to layer 4 cortical neurons initiates before that of intracortical inputs.

Anterior insular cortex activity predicts how well we attend to our bodily signals, while lesions to this brain region disrupt this ability.