Purpose: To improve simultaneous multislice (SMS) EPI by robust Nyquist ghost correction in both coil sensitivity calibration and SMS reconstruction.
Methods: To derive coil sensitivity and slice-dependent phase difference map between positive- and negative-echo images, single-band EPI reference data are fully sampled with EPI parameters matched to SMS acquisition. First, the reference data are organized into positive- and negative-echo virtual channels where missing data are estimated using low-rank-based simultaneous autocalibrating and k-space estimation (SAKE) at small matrix size. The resulting ghost-free positive- and negative-echo images are combined to generate coil sensitivity maps. Second, full-matrix positive- and negative-echo images are SENSE reconstructed from the reference data. Their phase difference or error map is then calculated. Last, SMS EPI is reconstructed using phase error correction SENSE (PEC-SENSE) that incorporates phase error map into coil sensitivity maps for negative-echo data. The proposed method was evaluated using both experimental data from 7T systems and simulations.
Results: Virtual coil SAKE eliminated Nyquist ghosts in the single-band EPI, yielding high-quality coil sensitivity maps and phase error maps. The subsequent PEC-SENSE robustly reconstructed SMS EPI under various conditions, including presence of in-plane acceleration, with lesser artifacts and higher temporal SNR than slice-dependent 1D linear correction method.
Conclusion: The proposed procedure of virtual coil SAKE calibration and PEC-SENSE reconstruction substantially reduces all ghost-related artifacts originating either directly from SMS EPI data or indirectly from EPI-based coil sensitivity maps. It is computationally efficient, and generally applicable to all SMS EPI-based applications.
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http://dx.doi.org/10.1002/mrm.27120 | DOI Listing |
J Mater Chem B
January 2025
Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Inspired from heat shock proteins (HSPs), a thermo-sensitive coacervate-forming polycaprolactone (CPCL) was designed as a natural chaperone mimic to protect proteins from thermal stress. Unlike the coil-globule polymers of poly(-isopropyl acrylamide) (PNIPAM), the as-designed CPCL underwent a partial dehydration during heating, characterizing it as a coacervate-forming polymer. With its ability to transform between the coil and coacervate states in response to temperature, theCPCL spontaneously captured and released targeted proteins, thereby behaving like a natural chaperone of HSPs.
View Article and Find Full Text PDFJ Magn Reson
January 2025
Department of Chemistry, Seoul National University, Seoul 08826 Republic of Korea; Advanced Institutes of Convergence Technology, Suwon 16229 Republic of Korea. Electronic address:
Most NMR samples are cylindrical, which is ideal for obtaining high-resolution NMR spectra, especially in superconducting magnets with a vertical bore. However, expanding NMR applicability to samples that are not necessarily cylindrical requires a new approach. In this study, we introduce a method for obtaining solution NMR signals from flat samples, such as flat containers or layered structures like a fuel cell.
View Article and Find Full Text PDFNeurosurg Rev
January 2025
Department of Neurosurgery, Carl Von Ossietzky University Oldenburg, Oldenburg, Germany.
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View Article and Find Full Text PDFAcad Radiol
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Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD (O.T.E., E.C.Y., B.D.S., S.A.H., D.G.G., Y.L., M.J.B., P.L.C., B.T.). Electronic address:
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J Neuroophthalmol
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Division of Ophthalmology (EB-S, AS, AA-A, AS-B, DW, SS, FC), Department of Surgery, University of Calgary, Calgary, Canada; Department of Biomedical Engineering (CN), University of Calgary, Calgary, Canada; Departments of Neurology (LBDL) and Ophthalmology (LBDL), University of Michigan, Ann Arbor, Michigan; and Department of Clinical Neurosciences (SS, FC), University of Calgary, Calgary, Canada.
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