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T1 - Cerebral magnetic resonance image synthesis

T1 - Design of resonance damping via control synthesis

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T1 - Magnetic resonance image example-based contrast synthesis

Magnetic resonance imaging (MRI) is widely used for analyzing human brain structure and function. MRI is extremely versatile and can produce different tissue contrasts as required by the study design. For reasons such as patient comfort, cost, and improving technology, certain tissue contrasts for a cohort analysis may not have been acquired during the imaging session. This missing pulse sequence hampers consistent neuroanatomy research. One possible solution is to synthesize the missing sequence. This paper proposes a data-driven approach to image synthesis, which provides equal, if not superior synthesis compared to the state-of-the-art, in addition to being an order of magnitude faster. The synthesis transformation is done on image patches by a trained bagged ensemble of regression trees. Validation was done by synthesizing T 2-weighted contrasts from T1-weighted scans, for phantoms and real data. We also synthesized 3 Tesla T1-weighted magnetization prepared rapid gradient echo (MPRAGE) images from 1.5 Tesla MPRAGEs to demonstrate the generality of this approach.

STOCHASTIC RESONANCE SOUND SYNTHESIS

ADSR envelopes are often used to control the volume of a sound, although they can be used to control almost anything inside a modular synthesizer. For example, the same envelope could control a resonant low pass filter, making a cool sweeping and wooshing effect evolve as we play each note.

Cerebral magnetic resonance image synthesis — Mayo …

The crystallization dynamics in wet-chemical synthesis is the key parameter controlling nanoparticlemorphology, which determines the frequency of the optical plasmon resonance in metal nanoparticles.

Angled silver/silver (Ag/Ag) homojunction nanowires (HNWs) with an average diameter of about 72 nm have been prepared by a straightforward and effective solvothermal method. The synthesis involves a one-step, non-seed, and template-less process to large-scale Ag/Ag HNWs, which is low-cost and proceeds at moderate temperatures. Two neighboring Ag nanorods or nanowires were connected into obtuse angle by Ag/Ag homojunction. It was found that synthesizing Ag/Ag HNWs were very sensitive to reaction temperature and polyvinylpyrrolidone concentration. Only through finely controlling these reaction parameters, the high-quality Ag/Ag HNWs could be formed in large scale and their surface plasmon resonance properties could be effectively tailored. High-resolution transmission electron microscopy and selected area electron diffraction investigations showed that the Ag/Ag HNWs were generated with a twinned crystalline structure. We also proposed a primary experimental model to illustrate the growth mechanism of the angled Ag/Ag HNWs.

Magnetic Resonance Tissue Contrast Synthesis | …

Let's add an LFO to our synthesizer that causes the pitch of our oscillator to wiggle up and down a little bit, like a violinist moves their hand to create vibrato. We're also going to use the envelope generator to modulate the frequency of our filter, so we get a cool sweeping effect automatically on every note, especially if we turn up the filter's resonance. Using a control signal to change the frequency of another module is called , or , as indicated in the diagram below:

Solutions of Ag and Au nanoparticles are strongly colored because of localized surface plasmon resonance in the UV/visible spectral region. The optical properties of these nanoparticles may be tuned to suit the needs of the application. This article summarizes our work in recent years on the solution synthesis of nanoparticles with tunable optical properties. The systems of interest include zero-dimensional bimetallic Ag–Au nanoparticles with different structures, one-, two-, and three-dimensional anisotropic monometallic Ag or Au nanoparticles. All of these nanosystems were prepared from colloidal synthesis through simple changes in the synthesis conditions. This is a demonstration of the versatility of colloidal synthesis as a convenient scalable technique for tuning the properties of metallic nanoparticles.

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  • Synthesis, EPR, ENDOR and TRIPLE resonance …

    Synthesis, multi-nonlinear dielectric resonance and electromagnetic absorption properties of hcp-cobalt particles

  • Design of resonance damping via control synthesis — …

    MAGNETIC RESONANCE IN CHEMISTRY, VOL. 31, 468-471 (1993) Synthesis, EPR, ENDOR and TRIPLE Resonance Investigations of …

  • Synthesis ranking with critic resonance

    Synthesis of Stiffness Parameters of Vibro-Impact Resonance Machines with Technological Limitations

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Cutoff and Resonance Explained - Image-Line

AB - Magnetic resonance imaging (MRI) is widely used for analyzing human brain structure and function. MRI is extremely versatile and can produce different tissue contrasts as required by the study design. For reasons such as patient comfort, cost, and improving technology, certain tissue contrasts for a cohort analysis may not have been acquired during the imaging session. This missing pulse sequence hampers consistent neuroanatomy research. One possible solution is to synthesize the missing sequence. This paper proposes a data-driven approach to image synthesis, which provides equal, if not superior synthesis compared to the state-of-the-art, in addition to being an order of magnitude faster. The synthesis transformation is done on image patches by a trained bagged ensemble of regression trees. Validation was done by synthesizing T 2-weighted contrasts from T1-weighted scans, for phantoms and real data. We also synthesized 3 Tesla T1-weighted magnetization prepared rapid gradient echo (MPRAGE) images from 1.5 Tesla MPRAGEs to demonstrate the generality of this approach.

Cutoff is used to block certain frequencies from a sound

N2 - Magnetic resonance imaging (MRI) is widely used for analyzing human brain structure and function. MRI is extremely versatile and can produce different tissue contrasts as required by the study design. For reasons such as patient comfort, cost, and improving technology, certain tissue contrasts for a cohort analysis may not have been acquired during the imaging session. This missing pulse sequence hampers consistent neuroanatomy research. One possible solution is to synthesize the missing sequence. This paper proposes a data-driven approach to image synthesis, which provides equal, if not superior synthesis compared to the state-of-the-art, in addition to being an order of magnitude faster. The synthesis transformation is done on image patches by a trained bagged ensemble of regression trees. Validation was done by synthesizing T 2-weighted contrasts from T1-weighted scans, for phantoms and real data. We also synthesized 3 Tesla T1-weighted magnetization prepared rapid gradient echo (MPRAGE) images from 1.5 Tesla MPRAGEs to demonstrate the generality of this approach.

Tetrahedron 61 (2005) 9996–10006

T1 - Synthesis, Vibrational Spectra, and Proton Magnetic Resonance of Some Boron-Substituted Tris(cyclopentadienyl)uranium(IV) Tetrahydroborates

Isocyanides are best shown as a mixture of both resonance structures

Fluorescence (FL)/magnetic resonance (MR) dual-modal imaging nanoprobes are significant not only for cutting edge research in molecular imaging, but also for clinical diagnosis with high precision and accuracy. However, synthesis of FL/MR dual-modal imaging nanoprobes that simultaneously exhibit strong fluorescent brightness and high MR response, long-term colloidal stability with uniform sizes, good biocompatibility and a versatile surface functionality has proven challenging. In this study, the well-defined core–shell structured Gd3+ chelate-conjugated fluorescent polymer nanoparticles (Gd-FPNPs) that consist of rhodamine B (RB)-encapsulated poly(methyl methacrylate) (PMMA) cores and Gd3+ chelate-conjugated branched polyethylenimine (PEI) shells, are facilely synthesized via a one-step graft copolymerization of RB-encapsulated MMA from PEI-DTPA-Gd induced by -butyl hydroperoxide (TBHP) at 80 °C for 2 h. The mild synthesis route not only preserves the chemical environment for Gd3+ coordination, but also improves optical properties and chemo-/photostability of RB. A high local concentration of outer surface-chelated Gd3+ and their direct interactions with hydrogen protons endow Gd-FPNPs high longitudinal relaxivity (26.86 mM–1 s–1). The uniform spherical structure of Gd-FPNPs facilitates their biotransfer, and their surface carboxyl and amine groups afford them both long-term colloidal stability and cell-membrane permeability. The excellent biocompatibility and FL/MR dual-modal imaging capability of Gd-FPNPs are demonstrated using HeLa cells and mice as models. All the results confirm that Gd-FPNPs fulfill the design criteria for a high-performance imaging nanoprobe. In addition, this study enables such probes to be prepared also by those not skilled in nanomaterial synthesis, and thus promoting the development of novel functional imaging nanoprobes.

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