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1 059 protocols using discovery mr750

1

Whole-brain MRI Acquisition for Alcoholism

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Whole-brain structural and functional MRI data were acquired using a 3T General Electric (GE) Signa scanner (9 controls and 4 alcoholics) and using a 3T GE Discovery MR750 (17 controls and 20 alcoholics) with an 8-channel head coil. Subject motion was minimized by following best practices for head fixation and image series were inspected for residual motion. Whole-brain fMRI data were acquired with a T2*-weighted gradient echo-planar pulse sequence (2D axial, echo time [TE] = 30 ms, repetition time [TR] = 2200 ms, flip angle = 90°, matrix = 64 × 64, slice thickness = 5 mm, 36 slices). A dual-echo fast spin-echo (FSE) sequence (2D axial acquisition; TE = 17/102 ms, TR = 8585ms, FOV = 24 cm, matrix = 256 × 192 matrix, NEX = 1.0, slice thickness = 2.5 mm, 62 slices) was used for spatially registering the fMRI data. A field map for correction of spatial distortions in the echo-planar images was generated from gradient-recalled echo (GRE) sequence with the following parameters for the 3T GE Signa scanner (TE = 3/5 ms, TR = 460 ms, slice thickness = 5 mm, 36 slices) and for the 3T GE Discovery MR750 (TE = 7/9 ms, TR = 1000 ms, slice thickness = 5 mm, 32 slices.)
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2

Relaxometric Properties of SPIO Nanoparticles

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Ultrafine SPIO@PEG aqueous samples with different Fe concentrations (0.05, 0.1, 0.2, 0.3, 0.4, and 0.5 mmol L−1) were prepared and placed in 2 mL test bottles. Longitudinal and transverse relaxation times (T1 and T2) were measured at room temperature at 0.5 T (magnetic resonance developer relaxation rate analyzer, NIUMAG, Suzhou, China), 1.5 T (Minispec Mq60 NMR Analyzer, Bruker, Beijing, China), and 3.0 T (Discovery MR750, GE Medical System, Milwaukee, WI), respectively. The T1 and T2 relaxivities (r1 and r2, mM−1 s−1) were determined by the curve fitting of T1 and T2vs. Fe concentration. MR imaging of samples was performed under a clinical 3.0 T MR scanner (Discovery MR750, GE Medical System, Milwaukee, WI). Axial images of the phantoms were acquired by T1-weighted spin-echo sequence (repetition time = 200 ms, echo time = 9 ms, matrix = 320 × 320, field of view = 18 × 18 cm, slice thickness = 3 mm, flip angle = 90°) and T2-weighted spin echo sequence (repetition time = 2500 ms, echo time = 100 ms, matrix = 320 × 320, field of view = 18 × 18 cm, slice thickness = 3 mm, flip angle = 90°).
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3

Magnetic Resonance Imaging of SPIO Micelles

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Magnetic resonance imaging (MRI) was used to assess the magnetic properties of bare SPIO, Dex-PLGA/DOX/SPIO and A54-Dex-PLGA/DOX/SPIO micelles. Bare SPIO and DOX/SPIO-loaded micelles solutions were diluted at various Fe3O4 concentrations of 100, 50, 25, 15, 10, 1, 0 μg mL−1. R2 relaxivities, defined as 1/T2 with units of s−1, of micelles solution were measured at room temperature with a 3.0 T clinical MRI system (GE, Discovery MR 750, USA). The parameters were as followed:FOV = 180 × 180 mm, TR = 2000 ms, TE = 12 ms, slice thickness = 3.0 mm, number of slices = 8.
BEL-7402 and HepG2 cells were incubated with Dex-PLGA/DOX/SPIO and A54-Dex-PLGA/DOX/SPIO micelles for 1 h. After the medium was discarded and the cells were washed with PBS three times, the cells were mixed with 200 μL agarose gel and stored at room temperature. The T2-weighted images were acquired using a 3.0 T clinical MRI system (GE, Discovery MR 750, USA). The parameters were as the above description.
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4

Evaluation of CUBE and CUBE-CS on MRI Phantoms

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Cube and Cube-CS were performed on a phantom set made of four tubes with gelatin gel (Sigma-Aldrich, Co. LLC., St. Louis, MO) at different percent weight varying from 20% to 50% with a T2 relaxation time range between 28ms and 156ms and a low resolution phantom filled with 0.18mmol/L ferumoxides solution (Feridex I.V., Advanced Magnetics, Inc., Cambridge, MA) with cylinders of diameters varying from 2mm to 12mm using the same 3T scanner (Discovery MR750, GE Healthcare, Waukesha, WI) and 8-channel phased-array extremity coil (Precision Eight TX/TR High Resolution Knee Array, InVivo, Orlando, Florida). CUBE and CUBE-CS were also performed on the American College of Radiology 0.9mm high resolution MRI phantom (American College of Radiology, Reston, VA) using the same 3T scanner (Discovery MR750, GE Healthcare, Waukesha, WI) and 16-channel wrap coil (GEM Flex, GE Healthcare, Waukesha, WI). The 8-channel extremity coil could not be used to image the American College of Radiology MRI phantom due to its large size. The phantom experiments were performed using the same CUBE and CUBE-CS imaging parameters as described for human subjects.
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Multi-Modal Brain Imaging Protocol

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MRI was performed with a 3 tesla Discovery MR 750 scanner (General Electric, Milwaukee, WI), and PET data were acquired with a Discovery PET/CT 690 (General Electric) at both time points.
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6

Comprehensive Brain MRI Characterization in Cerebral Palsy

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All brain MRI scans were acquired on a 3.0T MR scanner (Discovery MR750, GE Medical Systems, USA). Imaging sequences included transverse T1-weighted (T1W), T2-weighted (T2W), T2-fluid attenuated inversion-recovery (FLAIR), and sagittal T1W imaging, with a section of 4–5 mm thick. No enhanced scanning was performed in all cases. The obtained brain MRI images were evaluated by the pediatric neuroradiologists and CP specialists participating in our study. The findings were divided into periventricular white matter injury (PWMI): periventricular leukomalacia (PVL), ventriculomegaly; diffuse brain injuries: subcortical softening foci, myelin dysplasia, cerebral atrophy, basal ganglia/thalamic lesions; focal lesions: focal cerebral ischemia, porencephalia; cerebral dysplasia: dysplasia of the corpus callosum, cerebellar dysplasia; and normal brain MRI imaging.
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7

Multimodal MRI acquisition protocol

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All magnetic resonance imaging (MRI) data were acquired on a 3.0-Tesla Discovery MR750 scanner (General Electric, Milwaukee, WI) with an eight-channel receive coil. The 3D T1-weighted structural MRI (sMRI) data were obtained using a brain volume (BRAVO) sequence with the following parameters: repetition time (TR) /echo time (TE) /inversion time (TI) = 8.16/3.18/450 ms; field of view (FOV) = 256 mm × 256 mm; matrix = 256 × 256; flip angle (FA) = 12°; slice thickness = 1 mm; and 188 slices. The resting-state pseudo-continuous arterial spin labeling (ASL) data were obtained using a 3D spiral spin-echo sequence and background suppression: TR / TE = 5046/11.09 ms; post labeling delay (PLD) = 2025 ms; FOV = 240 mm × 240 mm; matrix = 128 × 128; flip angle (FA) = 111°; slice thickness = 3 mm; and 50 slices. Moreover, the resting-state functional MRI (rfMRI) data were obtained using a single-shot gradient-recalled-echo echo-planar-imaging (SS-GRE-EPI) sequence: TR/TE = 2000/30 ms; FOV = 220 mm × 220 mm; matrix = 64 × 64; FA = 90°; slice thickness = 3 mm; gap = 1 mm; 36 slices; and 180 volumes.
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8

3T MRI and Resting-State fMRI of Brain

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MRI scans were performed on a 3.0-Tesla magnetic resonance scanner (GE Healthcare Discovery MR750) in the Department of Radiology at the Affiliated Hospital of CDUTCM. A high-resolution 3D T1-weighted brain volume (BRAVO) MRI sequence was applied with the following parameters: repetition time (TR) = 8.16 ms, echo time (TE) = 3.18 ms, flip angle = 7°, field of view (FOV) = 256 × 256 mm2, in-plane resolution = 1 × 1 × 1 mm3, and 188 slices. Resting-state fMRI were obtained with a gradient-echo T2*-weighted echo-planar imaging sequence (GRE-EPI): time point = 201, TR/TE = 2000/30 ms, matrix = 64 × 64 × 30, voxel size = 3.5 × 3.5 × 4.02 mm3, flip angle = 90°). During the MRI, all patients were instructed to relax with their eyes closed without falling asleep.
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9

MRI Acquisition of Brain Structural and Functional Data

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MRI data were acquired by using a 3.0-Tesla MR system (Discovery MR750, General Electric, Milwaukee, WI, USA). We used tight, comfortable foam padding to reduce subject head movement, and earplugs were used to reduce noise from the scanner. 3D T1-weighted images were acquired by using a brain volume (BRAVO) sequence with the following parameters: repetition time (TR) = 8.16 ms; echo time (TE) = 3.18 ms; inversion time (TI) = 450 ms; flip angle (FA) = 12°; field of view (FOV) = 256 mm × 256 mm; matrix = 256 × 256; slice thickness = 1 mm, no gap; 184 sagittal slices; and acquisition time = 357 s. BOLD images were acquired by using a GRE-SS-EPI sequence with the following parameters: TR/TE = 2,000/35 ms; FOV = 220 mm × 220 mm; matrix = 64 × 64; FA = 90°; slice thickness = 3 mm; gap = 0.5 mm; 36 interleaved transverse slices; 185 volumes; and acquisition time = 370 s. We asked all subjects to close their eyes during the MRI scan, move as little as possible, not think about anything in particular, but not fall asleep. To ensure that only images without visible artifacts were included in the analysis, all MR images were visually inspected.
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10

Multi-modal Neuroimaging Protocol for Brain Mapping

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Structural MRI and DTI data were acquired from each subject on a 3-T MRI scanner (Discovery MR750, GE Medical system, Waukesha, WI, United States). Structural T1-weighted FSPGR BRAVO scans were obtained (120 axial slices, FOV = 512 mm × 512 mm, TR = 7232 ms, TE = 2.78 ms, in-plane voxel dimensions 0.5 mm × 0.5 mm, slice thickness = 1.5 mm). For the DTI protocol, a 12-min DTI (HARDI) scan was collected in 55 diffusion weighted directions (b = 3000 s/mm2, TR = 9313 ms, TE = 76.6 ms, FOV = 256 mm × 256 mm, in-plane voxel dimensions = 2 mm × 2 mm, axial slice thickness = 2 mm).
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