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Signa 3 tesla mri scanner

Manufactured by GE Healthcare
Sourced in United States

The Signa 3 Tesla MRI scanner is a magnetic resonance imaging system manufactured by GE Healthcare. It operates at a magnetic field strength of 3 Tesla, which allows for high-resolution imaging and improved signal-to-noise ratio. The Signa 3 Tesla MRI scanner is designed for diagnostic imaging applications.

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4 protocols using signa 3 tesla mri scanner

1

Amyloid-β PET Imaging Protocol

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PIB PET scans were performed at CUMC Kreitchman PET Center (n=45) on an ECAT EXACT HR+ (Siemens, Knoxville, TN) or Weill Cornell Medicine Citigroup Biomedical Imaging Center (n=32) on a Siemens Biograph mCT. Immediately following 30-second intravenous PIB injection, dynamic images were acquired in 3D mode at 3 × 20 sec, 3 × 1 min, 3 × 2 min, 2 × 5 min, and 7 × 10 min. Low-dose CT scan was performed for attenuation correction. A 3D SPGR T1 Sequence was performed on a GE Signa 3 Tesla MRI scanner. PET scans were performed within one year of UPSIT (mean interval = 93.9 ± 93.1 days), with the exception of one subject who had PET scan performed 16.5 months after UPSIT.
PET analysis was performed using PMOD 3.6. MR images were segmented using the PNEURO tool and the Hammers-N30R83–1MM atlas was used to define regions-of-interest (ROIs). ROIs were inspected and manually corrected if necessary. PET images 50–70 min post-injection were averaged, co-registered to the corresponding MR image, and individual subject ROIs were then applied. Mean uptake over 50–70 min from a composite gray matter ROI from frontal, parietal, and lateral temporal cortex (excluding sensorimotor cortex) was divided by mean uptake in cerebellar gray matter to create a global standardized uptake value ratio (SUVR). PIB SUVR > 1.5 was used to define amyloid-β positivity [22 (link), 23 (link)].
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2

Functional MRI of Working Memory Tasks

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Image acquisition was performed using a General Electric Signa 3 Tesla MRI scanner at the Brain Research Institute, Melbourne. Both WM tasks were displayed via a video projector onto a screen inside the magnet room, and viewed through a mirror mounted above participants' eyes. The image subtended 8° vertically and 12° horizontally when viewed from an effective distance of 4 m. Participant responses and reaction time were recorded through a response box that fed back into the stimuli presentation computer running Authorware. Participants were asked to press the right button for “same” and the left button for “different.” T2* weighted functional images were acquired during WM task performance (TR = 2500 ms, TE = 40 ms, flip angle = 60°, FOV = 240 mm, matrix = 96 × 96, 26 slices, 1 mm spacing, in plane resolution = 2.5 mm). High resolution 3-D T1 weighted anatomical images were also acquired (slices = 124, thickness = 1.4 mm, FOV = 240 mm, matrix = 512 × 256, flip angle = 20°).
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3

3-Tesla MRI Brain Imaging Protocol

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Image data were acquired with a GE Signa 3-Tesla MRI scanner (max gradient strength 40 mT/m, max gradient slew rate 150 T/m/s; General Electric Company, Waukesha, Wisconsin, USA) with pre-processing following previously published methods (Pergolizzi et al., 2019 (link)) (supplemental material).
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4

Multimodal MRI Acquisition Protocol

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Structural and functional brain images were obtained using a GE Signa 3-Tesla MRI scanner, located at the University of Michigan Functional Magnetic Resonance Imaging Laboratory. A 16-rod bird cage head coil was used for all participants, and movement was minimized by using head cushions and Velcro straps. During each participant’s scanning session, we acquired T1-weighted structural images, high-resolution structural images using spoiled 3D gradient-echo acquisition (SPGR), and T2*-weighted functional images (one resting state scan including 240 volumes and one task-based scan including 180 volumes). Functional images were obtained using a single-shot gradient-echo (GRE) reverse spiral pulse sequence. The field of view was 220 × 200 mm, the voxel size was 3 × 3 × 4 mm (40 axial slices), the TR (repetition time) was 2 seconds, and the TE (echo time) was 30 ms. Respiratory and cardiac data were collected for both resting state and task scans, and were subsequently controlled for in first-level analyses.
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