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  • B R Conway
  • 2001
The spatial structure of color cell receptive fields is controversial. Here, spots of light that selectively modulate one class of cones (L, M, or S, or loosely red, green, or blue) were flashed in and around the receptive fields of V-1 color cells to map the spatial structure of the cone inputs. The maps generated using these cone-isolating stimuli and an(More)
Imaging studies are consistent with the existence of brain regions specialized for color, but electrophysiological studies have produced conflicting results. Here we address the neural basis for color, using targeted single-unit recording in alert macaque monkeys, guided by functional magnetic resonance imaging (fMRI) of the same subjects. Distributed(More)
Neurons in the lateral geniculate nucleus cannot perform the spatial color calculations necessary for color contrast and color constancy. Under neutral-adapting conditions, we mapped the cone inputs (L, M, and S) to 83 cone-opponent cells representing the central visual field of the next stage of visual processing, primary visual cortex (V1), to determine(More)
Internalization and transport of a ligand-receptor complex are required to initiate cell body responses to target-derived neurotrophin. However, it is not known whether internalized receptors and cell surface receptors initiate the same signaling pathways and biological responses. Here we use a temperature-sensitive mutant of dynamin (G273D) to control the(More)
Color has become a premier model system for understanding how information is processed by neural circuits, and for investigating the relationships among genes, neural circuits, and perception. Both the physical stimulus for color and the perceptual output experienced as color are quite well characterized, but the neural mechanisms that underlie the(More)
Color processing begins with the absorption of light by cone photoreceptors, and progresses through a series of hierarchical stages: Retinal signals carrying color information are transmitted through the lateral geniculate nucleus of the thalamus (LGN) up to the primary visual cortex (V1). From V1, the signals are processed by the second visual area (V2);(More)
Binocular simple cells in primary visual cortex (V1) are the first cells along the mammalian visual pathway to receive input from both eyes. Two models of how binocular simple cells could extract disparity information have been put forward. The phase-shift model proposes that the receptive fields in the two eyes have different subunit organizations, while(More)
We used two-dimensional (2-D) sparse noise to map simultaneous and sequential two-spot interactions in simple and complex direction-selective cells in macaque V1. Sequential-interaction maps for both simple and complex cells showed preferred-direction facilitation and null-direction suppression for same-contrast stimulus sequences and the reverse for(More)
The contribution that different brain areas make to primate color vision, especially in the macaque, is debated. Here we used functional magnetic resonance imaging in the alert macaque, giving a whole brain perspective of color processing in the healthy brain. We identified color-biased and luminance-biased activity and color-afterimage activity.(More)
The primate visual system is arranged hierarchically, starting from the retina and continuing through a series of extrastriate visual areas. Selectivity for motion is first found in individual neurons in the primate visual cortex (V1), in which many simple cells respond selectively to the direction and speed of moving stimuli. Beyond simple cells, most(More)