It is a well-known property in Fourier transform magnetic resonance imaging (MRI) that rigid body translational motion in image space results in linear phase accumulation in k -space. This work describes Multiple Overlapping k-space Junctions for Investigating Translating Objects (MOJITO), a correction scheme based on phase differences at trajectory intersections caused by 2-D alterations in the position of an object during MR imaging. The algorithm allows both detection and correction of motion artifacts caused by 2-D rigid body translational motion. Although similar in concept to navigator echoes, MOJITO does not require a repeating path through k-space, uses k-space data from a broader region of k -space, and uses the repeated data in image reconstruction; this provides the potential for a highly efficient self-navigating motion correction method. Here, the concept and theoretical basis of MOJITO is demonstrated using the continuous sampling BOWTIE trajectory in simulation and MR experiments. This particular trajectory is selected since it is well suited for such an algorithm due to numerous trajectory intersections. Specifically, the validity of the technique in the presence of noise and off-resonance effects is demonstrated through simulation.
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http://dx.doi.org/10.1109/TMI.2009.2029854 | DOI Listing |
Metab Brain Dis
January 2025
Department of Biomedical and Biotechnological Sciences, Human Anatomy and Histology Section, School of Medicine, University of Catania, Catania, Italy.
SERPINA3, a serine protease inhibitor, is strongly associated with neuroinflammation, a typical condition of AD. Its expression is linked to microglial and astrocytic markers, suggesting it plays a significant role in modulating neuroinflammatory responses. In this study, we examined the SERPINA3 expression levels, along with CHI3L1, in various brain regions of AD patients and non-demented healthy controls (NDHC).
View Article and Find Full Text PDFBMC Mol Cell Biol
January 2025
Epigenetics Programme, Babraham Institute, Cambridge, CB22 3AT, UK.
Background: During the latter stages of their development, mammalian oocytes under dramatic chromatin reconfiguration, transitioning from a non-surrounded nucleolus (NSN) to a surrounded nucleolus (SN) stage, and concomitant transcriptional silencing. Although the NSN-SN transition is known to be essential for developmental competence of the oocyte, less is known about the accompanying molecular changes. Here we examine the changes in the transcriptome and DNA methylation during the NSN to SN transition in mouse oocytes.
View Article and Find Full Text PDFBiosystems
January 2025
Interpretation Laboratory, UCSB, USA; Interpretation Laboratory, ASB, Switzerland. TU Delft. Electronic address:
This article revisits Artificial Neural Networks (NNs) through the lens of Evolutionary Dynamics. The two most important features of NNs are shown to reflect the two most general processes of Evolutionary Dynamics. This overlap may serve as a new and powerful connection between NNs and Evolutionary Dynamics, which encompasses a body of knowledge that has been built over multiple centuries and has been expanded to inspire applications across a vast range of disciplines.
View Article and Find Full Text PDFRev Alerg Mex
December 2024
Departamento de Inmunología, Hospital Infantil de Especialidades de Chihuahua; Facultad de Medicina y Ciencias Biomédicas, Universidad Autónoma de Chihuahua.
Background: 22q11 deletion syndrome consists of a variable grouping of phenotypic features and immunological defects secondary to the loss of genetic material located in the 22q11.2 band. The 22q11 deletion spectrum encompasses different syndromes related to the same etiology and with overlapping anomalies, including DiGeorge syndrome, velocardiofacial syndrome, among others.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
The University of Sydney, Sydney, NSW, Australia.
Background: Hyperphosphorylated tau (pTau) in Alzheimer's disease (AD) brain tissue is a complex mix of multiple tau species that are variably phosphorylated on up to 55 epitopes. Emerging studies suggest that phosphorylation of specific epitopes may alter the role of tau. The role of specific pTau species can be explored through protein interaction ("interactome") studies.
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