This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Introduction: Neural microstimulation experiments in the superior colliculus (SC) of primates enhanced performance in a spatially selective manner while they maintained fixation, suggesting a role for covert visual attention in SC (e.g., M?ller et al, 2004; Cavenaugh, et al., 2006). Previous fMRI experiments have shown a rough retinotopic organization in human SC corresponding to direct visual stimulus (Shneider &Kastner, 2005). We performed experiments to determine if retinotopically organized signals corresponding to covert visual attention were present in human SC. At the same time, we developed methods to examine the laminar distribution of hemodynamic activity in the depth of the SC. Methods: We measured the retinotopic organization of SC to direct visual stimulation using a wedge of flickering dots (eccentricity 1?9?, azimuthal width 144?) that slowly rotated (24-s period) around the fixation mark. To measure the retinotopy of covert attention, we used a full-field flickering (4-Hz) grating (1 cpd) stimulus at 60% contrast. Subjects were cued to perform a difficult contrast decrement-discrimination task within a region (eccentricity 1?9?, azimuthal width 90?) that slowly rotated (24-s period) in azimuth around fixation. High-resolution fMRI (1.3 mm cubic voxels) data were acquired (3 s/volume) on 8 slices within SC (orientation perpendicular to the neuraxis) using a 3 shot spiral sequence and a TE of 45 ms. These data were then aligned to a high-resolution (0.6-mm voxels) T1-weighted reference volume. The SC was segmented in this volume so that the surface of the SC could be computationally flattened, and to permit computation of a depth map for laminar analysis

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR009784-15
Application #
7955411
Study Section
Special Emphasis Panel (ZRG1-SBIB-F (40))
Project Start
2009-06-01
Project End
2010-05-31
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
15
Fiscal Year
2009
Total Cost
$12,030
Indirect Cost
Name
Stanford University
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Maclaren, Julian; Aksoy, Murat; Ooi, Melvyn B et al. (2018) Prospective motion correction using coil-mounted cameras: Cross-calibration considerations. Magn Reson Med 79:1911-1921
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Kogan, Feliks; Hargreaves, Brian A; Gold, Garry E (2017) Volumetric multislice gagCEST imaging of articular cartilage: Optimization and comparison with T1rho. Magn Reson Med 77:1134-1141
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Bian, W; Tranvinh, E; Tourdias, T et al. (2016) In Vivo 7T MR Quantitative Susceptibility Mapping Reveals Opposite Susceptibility Contrast between Cortical and White Matter Lesions in Multiple Sclerosis. AJNR Am J Neuroradiol 37:1808-1815
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