Titlebook: Colour Vision Deficiencies XIII; Proceedings of the t C. R. Cavonius Conference proceedings 1997 Springer Science+Business Media Dordrecht

ASTER

Rod and cone inputs to parvo- and magnocellular cells in the dichromatic common marmoset (,) contrast gains of cells were obtained for each wavelength, from which their spectral sensitivities could be inferred. We found that up to relatively high luminances the cells received rod input, and that the rod input was never opponent to the cone input

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叢林

SCORE

Ramesh Senthinathan,John L. Princeme inhibitory interaction between the red and green responses begins. At the ganglion stage there is greatly enhanced red—green inhibition and amplification of the blue response. There is no significant change between the ganglion cells and the final common path, so it may be concluded that colour processing is complete in the retina.

Vertebra

Sensitivity and spectral tuning of the red-green chromatic pathway in heterozygous carriers of conge cone photopigment genes. This is consistent with the assumption that the primary effect of heterogeneity in the cone mosaic on sensitivity of the midget ganglion cell mosaic is to reduce the number of ganglion cells mediating detection.

斗爭

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crutch

Structure and function in primate retinanner, and that luminance and chromatic detection channels defined psychophysically have firm anatomical and physiological substrates at a retinal level. These results are reviewed, and it is suggested that parallel pathways beginning in the retina are best defined in terms of the anatomical mosaics of ganglion cell types in which they originate.

TAG

https://doi.org/10.1007/978-94-011-0743-3relative levels of expression of these genes into mRNA and protein in the retina. The red and green pigment genes exist in head-to-tail arrays: one red pigment gene is found 5′ upstream of one or more green pigment genes. In addition to normal red and green pigment genes, 5′green-red3′ hybrid genes,