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In this study, we applied a combination of head-fixed cylindrical-lens goggles and optical imaging of intrinsic signals to investigate postnatal orientation plasticity in kitten primary visual cortex.
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This variability has made it difficult to delineate the postnatal critical period during which orientation plasticity manifests.
Purkinje cell soma extend multiple dendrites in random orientations during the first postnatal week in mice.
In mice, Purkinje cell somas extend multiple dendrites in random orientations during the first postnatal week (supplementary material Fig. S4; Tanaka et al., 2006).
Orientation plasticity appears to have two phases: First, the visual cortical circuit is rendered highly modifiable in orientation selectivity during a brief postnatal critical period for 6 weeks; and second, modified orientation selectivity consolidates during continuous long-term single-orientation exposure.
Nonpatterned and patterned membranes were used for hippocampal neuronal cultures isolated from postnatal days 1 3 hamsters and the neurite length, orientation and specific functions of cells were investigated up to 12 days of culture.
In the present study, we showed a postnatal sensitive period profile for the modifiability of orientation selectivity in the visual cortex of kittens reared with head-mounted goggles for stable single-orientation exposure.
In this study, the orientation of dividing GNPs at different stages of postnatal cerebellar development has been characterized.
There is no proof that postnatal social environment has any crucial effect on gender identity or sexual orientation.
The presently delineated critical period for orientation plasticity overlaps the most sensitive period for ocular dominance plasticity (postnatal 4 5 weeks) [29].
But if as suggested, transcribed RTE sequences in postnatal mouse testes are mainly provided from co-transcription with genes, the transcriptional orientation of a given genic RTE loci is to a large extent determined by the orientation of the host gene.
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