The Journal of Neuroscience, August 8, 2007, ():
Functional Imaging of Primary Visual Cortex Using Flavoprotein Autofluorescence
J. Neurosci. Husson et al.
27: 8665
Supplemental Data
Files in this Data Supplement:
- supplemental material
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Supplementary Figure 1: Progression of fluorescence demonstrating the smooth retinotopic organization of mouse primary visual cortex. This is the average of responses to 80 stimulus presentations. (Animated GIF)
- supplemental material
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Supplementary Figure 2: Progression of intrinsic signals (light absorption) showing that AFI and ISI are 180° out-of-phase with each other. This is the average of responses to 80 stimulus presentations. (Animated GIF)
- supplemental material
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Supplementary Figure 3: A third example of orientation preference maps. A. Vascular pattern. B. Orientation map generated by AFI. C. Orientation map generated by ISI. The maps are similar over cortex, but differ in unresponsive and non-neural areas.
- supplemental material
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Supplementary Figure 4: Differences in orientation preference plotted in polar coordinates. A. Difference between measured AFI and ISI maps. B. Difference between AFI map and randomly shuffled ISI map (?, orientation; r, response strength).
- supplemental material
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Supplementary Figure 5: Time course of autofluorescence in cat Area 17 in response to a drifting horizontal grating. This is the average of responses to 16 stimulus presentations. Images have been spatially high-pass filtered. (Animated GIF)
- supplemental material
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Supplementary Figure 6: Time course of electrical stimulation in the cat with intervals of A. 15 and B. 35 seconds demonstrating a second peak in autofluorescence.
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Supplementary Figure 7: Progression of blue intrinsic signal during electrical stimulation, averaged over 20 trials. (Animated GIF)
- supplemental material
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Supplementary Figure 8: Progression of autofluorescence signal during electrical stimulation, averaged over 20 trials. (Animated GIF)
