The largest database of trusted experimental protocols

Signa pioneer 3.0t

Manufactured by GE Healthcare
Sourced in United Kingdom, United States

The Signa Pioneer 3.0T is a magnetic resonance imaging (MRI) system manufactured by GE Healthcare. It operates at a field strength of 3.0 Tesla and is designed to provide high-quality diagnostic images for a variety of medical applications.

Automatically generated - may contain errors

4 protocols using signa pioneer 3.0t

1

MRI Assessment of Temporal Muscle Thickness

Check if the same lab product or an alternative is used in the 5 most similar protocols
We collected data of age, sex, height, weight, and body mass index (BMI). We used SIGNA Pioneer 3.0T (GE Healthcare Life Sciences, Buckinghamshire, England) by a 24-channel head-neck coil and acquired MR images. We measured TMT on an axial plane of the T1-weighted image (T1WI) in the previously reported way.[39 ] Predefined anatomical landmarks, such as the Sylvian fissure (anterior-posterior orientation) and the orbital roof (craniocaudal orientation), were used to guarantee a high reproducibility of TMT values. Two investigators measured the TMT using SYNAPSE V 4.1.5 imaging software (Fujifilm Medical, Tokyo, Japan). TMT was assessed on both sides in each individual, and the mean TMT was calculated by summing up those measurements and dividing them by two. There were no individuals with muscle edema, atrophy due to craniotomy or radiation therapy, trigeminal nerve disease, nor myopathy, which might be related to smaller TMT.
According to the Fazekas scale, we also evaluated periventricular hyperintensity (PVH) on fluid-attenuated inversion recovery images.[9 (link)] We also counted the number of microbleeds on the T2* image and detected intracranial cerebral aneurysm on magnetic resonance angiography.
+ Open protocol
+ Expand
2

Resting-State fMRI Processing Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The MRI data were obtained from a GE Signa Pioneer 3.0T magnetic resonance scanner at the Third People’s Hospital of Foshan (Foshan Mental Health Center), Guangdong Province. A high-resolution T1-weighted structural image was obtained using a 3D-T1WI sequence, and resting-state data were collected using a GRE-SS-EPI sequence. The data underwent preprocessing using DPABI_V6.1, including removal of the first 10 time points, slice timing correction, realignment, normalization, smoothing, covariate regression, and band-pass temporal filtering (0.01–0.08 Hz). The fALFF analysis employed fast Fourier transform (FFT) to calculate power spectra and compute the square root of the power spectrum within the 0.01–0.08 Hz range to obtain fALFF values. The fALFF value represents the ratio of the power spectrum within the low-frequency range to that within the entire frequency range [30 (link)]. Only the rs-fMRI signals within the filtered slow-5 (0.01–0.027 Hz) and slow-4 (0.027–0.073 Hz) frequency bands were retained for subsequent analysis. Data quality control was performed using DPABI’s Quality Control program, discarding data with head motion exceeding 2.5 mm or rotation angles exceeding 2.5°.
+ Open protocol
+ Expand
3

Diffusion Kurtosis Imaging on 3T MRI

Check if the same lab product or an alternative is used in the 5 most similar protocols
MRI acquisition was performed on 3T MR scanner (GE Signa Pioneer 3.0T). Thirty minutes before examination, all participants were given chloral hydrate (0.5 ml/kg) enemas. For stable image quality, earplugs with cotton balls were used to keep them from noise from the machine. After routine sequences scan, axial DKI was performed on all participants. The scanning parameters were: TR/TE = 8,200 ms/2.3 ms, FOV = 200 mm×200 mm, acquisition matrix = 256 × 256, NEX = 1, slices thickness = 4 mm, number of slices = 27; gradient values b: 0, 1,000 and 2,000 s/mm2; scanning time = 7 min 23 s. All subjects had no apparent structural damage, who were examined by two radiologists based on conventional MRI images.
+ Open protocol
+ Expand
4

Comprehensive Multi-Technique Characterization of Magnetic Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphology and
particle size of the NPs were observed by field-emission TEM (JEM
2100F, JEOL, Japan) and field-emission scanning electron microscopy
(SEM) (SU8020, Hitachi, Japan). The active functional groups modified
on the surface of the particles were analyzed using a Fourier transform
infrared (FT-IR) spectrometer (Nicolet IS10, Nicolet, USA). The hydrodynamic
size and the surface potential were measured by dynamic light scattering
(Zetasizer Nano ZS90, Thermo Fisher, USA) and ζ potential analysis,
respectively. The concentration of Fe3+ was measured via
inductively coupled plasma atomic emission spectrometry (ICP-AES)
(Agilent ICPOES730, Agilent, USA). The ionic valency and crystal morphology
of the NPs were separately analyzed through X-ray photoelectron spectroscopy
(XPS) (Thermo ESCALAB 250Xi, Thermo Fisher, USA) and X-ray powder
diffraction (XRPD) (Bruker D8 ADVANCE, Bruker, Germany). A vibrating-sample
magnetometer (VSM) (SQUID-VSM MPMS-3, Quantum Design, USA) was employed
to measure the saturation magnetization value (Ms). Moreover, the characteristics of the element distribution
were analyzed by energy-dispersive spectroscopy (EDS), and MRI (SIGNA
Pioneer 3.0-T, GE, USA) was adopted for image acquisition and signal
analysis of different MRI sequences.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!