1,434 research outputs found

    Transcatheter Closure of Multiple Atrial Septal Defects With the Amplatzer Device

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    Percutaneous device occlusion of secundum atrial septal defect (ASD) has become an accepted alternative to surgical repair. A variety of devices have been used successfully. However, all of them have limitations. We report our experience with two devices used to close multiple ASDs

    A Large Intrathoracic Meningocele in a Patient with Neurofibromatosis-1

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    A large intrathoracic meningocele, a saccular protrusion of the meninges through a dilated intervertebral foramen or a bony defect of the vertebral column, was diagnosed in a 41-year-old female patient showing clinical features of neurofibromatosis-1 (NF-1), including café-au-lait spots, cutaneous neurofibromas, and axillary frecklings and Lisch nodules on the iris. Her daughter and son also had similar manifestations of NF-1. Regular follow-up with periodic imaging was recommended without surgical treatment because there were no signs or symptoms. Meningocele should be differentiated from posterior mediastinal tumors such as neurofibroma, neuroblastoma, and ganglioneuroma because NF-1 has a high risk of tumor formation. We report on this case with a brief review of the literature

    Block copolymer gyroids for nanophotonics: significance of lattice transformations

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    A gyroid crystal possesses a peculiar structural feature that can be conceptualized as a triply periodic surface with a constant mean curvature of zero. The exotic optical properties such as the photonic bandgap and optical chirality can emerge from this three-dimensional (3D) morphological feature. As such, gyroid crystals have been considered as the promising structures for photonic crystals and optical metamaterials. To date, several methods have been proposed to materialize gyroid crystals, including 3D printing, layer-by-layer stacking, two-photon lithography, interference lithography, and self-assembly. Furthermore, the discovery of Weyl points in gyroid crystals has further stimulated these advancements. Among such methods, the self-assembly of block copolymers (BCPs) is unique, because this soft approach can provide an easy-to-craft gyroid, especially at the nanoscale. The unit-cell scale of a gyroid ranging within 30–300 nm can be effectively addressed by BCP self-assembly, whereas other methods would be challenging to achieve this size range. Therefore, a BCP gyroid has provided a material platform for metamaterials and photonic crystals functioning at optical frequencies. Currently, BCP gyroid nanophotonics is ready to take the next step toward topological photonics beyond the conventional photonic crystals and metamaterials. In particular, the intrinsic lattice transformations occurring during the self-assembly of BCP into a gyroid crystal could promise a compelling advantage for advancing Weyl photonics in the optical regime. Lattice transformations are routinely considered as limitations, but in this review, we argue that it is time to widen the scope of the lattice transformations for the future generation of nanophotonics. Thus, our review provides a comprehensive understanding of the gyroid crystal and its lattice transformations, the relevant optical properties, and the recent progress in BCP gyroid self-assembly

    Genome-Scale Profiling and High-Throughput Analyses Unravel the Genetic Basis of Arsenic Content Variation in Rice

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    Ionomics, the study of the composition of mineral nutrients and trace elements in organisms that represent the inorganic component of cells and tissues, has been widely studied to explore to unravel the molecular mechanism regulating the elemental composition of plants. However, the genetic factors of rice subspecies in the interaction between arsenic and functional ions have not yet been explained. Here, the correlation between As and eight essential ions in a rice core collection was analyzed, taking into account growing condition and genetic factors. The results demonstrated that the correlation between As and essential ions was affected by genetic factors and growing condition, but it was confirmed that the genetic factor was slightly larger with the heritability for arsenic content at 53%. In particular, the cluster coefficient of japonica (0.428) was larger than that of indica (0.414) in the co-expression network analysis for 23 arsenic genes, and it was confirmed that the distance between genes involved in As induction and detoxification of japonica was far than that of indica. These findings provide evidence that japonica populations could accumulate more As than indica populations. In addition, the cis-eQTLs of AIR2 (arsenic-induced RING finger protein) were isolated through transcriptome-wide association studies, and it was confirmed that AIR2 expression levels of indica were lower than those of japonica. This was consistent with the functional haplotype results for the genome sequence of AIR2, and finally, eight rice varieties with low AIR2 expression and arsenic content were selected. In addition, As-related QTLs were identified on chromosomes 5 and 6 under flooded and intermittently flooded conditions through genome-scale profiling. Taken together, these results might assist in developing markers and breeding plans to reduce toxic element content and breeding high-quality rice varieties in future

    Atomic-scale Electronic Structure of the Cuprate Pair Density Wave State Coexisting with Superconductivity

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    The defining characteristic of hole-doped cuprates is dd-wave high temperature superconductivity. However, intense theoretical interest is now focused on whether a pair density wave state (PDW) could coexist with cuprate superconductivity (D. F. Agterberg et al., Annual Review of Condensed Matter Physics 11, 231 (2020)). Here, we use a strong-coupling mean-field theory of cuprates, to model the atomic-scale electronic structure of an eight-unit-cell periodic, dd-symmetry form factor, pair density wave (PDW) state coexisting with dd-wave superconductivity (DSC). From this PDW+DSC model, the atomically-resolved density of Bogoliubov quasiparticle states N(r,E) is predicted at the terminal BiO surface of Bi2_2Sr2_2CaCu2_2O8_8 and compared with high-precision electronic visualization experiments using spectroscopic imaging STM. The PDW+DSC model predictions include the intra-unit-cell structure and periodic modulations of N(r,E), the modulations of the coherence peak energy Δp\Delta_p (r), and the characteristics of Bogoliubov quasiparticle interference in scattering-wavevector space (q-space). Consistency between all these predictions and the corresponding experiments indicates that lightly hole-doped Bi2_2Sr2_2CaCu2_2O8_8 does contain a PDW+DSC state. Moreover, in the model the PDW+DSC state becomes unstable to a pure DSC state at a critical hole density p*, with empirically equivalent phenomena occurring in the experiments. All these results are consistent with a picture in which the cuprate translational symmetry breaking state is a PDW, the observed charge modulations are its consequence, the antinodal pseudogap is that of the PDW state, and the cuprate critical point at p* ~ 19% occurs due to disappearance of this PDW

    Barotraumatic Perforation of Pharyngoesophagus by Explosion of a Bottle into the Mouth

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    Pharyngoesophageal perforation from an exploding bottle is an extremely rare injury. To date, twenty-four cases have been documented in English literature. In this study, we reported two additional cases of pharyngoesophageal perforation by a bottle exploding in the mouth. Explosion of the bottle occurred when the patients removed the cap of a home-made wine bottle with their teeth, which resulted in pharyngoesophageal perforation. The patients were managed by conservative treatment and operative repair, respectively. Both patients had an uneventful recovery. Possible mechanisms and preventive measures are discussed in this study, along with a review of the literature

    Effects of Intronic and Exonic Polymorphisms of Paraoxonase 1 (PON1) Gene on Serum PON1 Activity in a Korean Population

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    Paraoxonase 1 (PON1) hydrolyzes a number of toxic organophosphorous compounds and reduces lipid peroxide accumulation, and PON1 genetic polymorphisms in the coding region modulate serum PON1 activity. In this study, we investigated the association between 3 polymorphisms of PON1 located in intron 5 (17899insdelTT and 17974CT) and exon 6 (192QR) and serum PON1 activity. The genetic polymorphisms and serum activity of PON1 were analyzed in 153 healthy Koreans by using a direct sequencing assay and spectrophotometric method, respectively. A significant linkage disequilibrium (LD) was observed between all tested single nucleotide polymorphisms, with the strongest LD observed between 17899insdelTT and 192QR (D' = 0.984). The 17899insdelTT, 17974CT and 192QR genetic polymorphisms were associated with significant differences in serum paraoxonase activity. In multiple regression analyses, smoking, triglyceride level, high-density lipoprotein (HDL) level, and the 17899insdelTT and 192QR genetic polymorphisms were significant determinants of serum paraoxonase activity, while age, smoking, triglyceride level, HDL level, and the 192QR genetic polymorphism were significant determinants of serum arylesterase activity. These results suggest that although the 192QR genetic polymorphism in the coding region of PON1 is primarily associated with serum PON1 activity, the intronic polymorphisms are also involved in serum PON1 activity, and this association may be mediated by LD
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