187 research outputs found

    Application of PDT for Uterine Cervical Cancer

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    We have been performing PDT using Excimer Dye Laser (EDL) or YAG-OPO laser, a type of low power laser, both of which have a considerably higher degree of tissue penetration even when compared to PDT using Argon Dye Laser (ADL)

    Evaluation of measurement accuracies of the Higgs boson branching fractions in the International Linear Collider

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    Precise measurement of Higgs boson couplings is an important task for International Linear Collider (ILC) experiments and will facilitate the understanding of the particle mass generation mechanism. In this study, the measurement accuracies of the Higgs boson branching fractions to the bb and cc quarks and gluons, ΔBr(Hbbˉ,ccˉ,gg)/Br\Delta Br(H\to b\bar{b},\sim c\bar{c},\sim gg)/Br, were evaluated with the full International Large Detector model (\texttt{ILD\_00}) for the Higgs mass of 120 GeV at the center-of-mass (CM) energies of 250 and 350 GeV using neutrino, hadronic and leptonic channels and assuming an integrated luminosity of 250fb1250 {\rm fb^{-1}}, and an electron (positron) beam polarization of -80% (+30%). We obtained the following measurement accuracies of the Higgs cross section times branching fraction (Δ(σBr)/σBr\Delta (\sigma \cdot Br)/\sigma \cdot Br) for decay of the Higgs into bbˉb\bar{b}, ccˉc\bar{c}, and gggg; as 1.0%, 6.9%, and 8.5% at a CM energy of 250 GeV and 1.0%, 6.2%, and 7.3% at 350 GeV, respectively. After the measurement accuracy of the cross section (Δσ/σ\Delta\sigma/\sigma) was corrected using the results of studies at 250 GeV and their extrapolation to 350 GeV, the derived measurement accuracies of the branching fractions (ΔBr/Br\Delta Br/Br) to bbˉb\bar{b}, ccˉc\bar{c}, and gg were 2.7%, 7.3%, and 8.9% at a CM energy of 250 GeV and 3.6%, 7.2%, and 8.1% at 350 GeV, respectively.Comment: 15 pages, 6 figure

    Repair of the TGFBI gene in human corneal keratocytes derived from a granular corneal dystrophy patient via CRISPR/Cas9-induced homology-directed repair

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    Abstract Granular corneal dystrophy (GCD) is an autosomal dominant hereditary disease in which multiple discrete and irregularly shaped granular opacities are deposited in the corneal stroma. GCD is caused by a point mutation in the transforming growth factor-β-induced (TGFBI) gene, located on chromosome 5q31. Here, we report the first successful application of CRISPR-Cas9-mediated genome editing for the correction of a TGFBI mutation in GCD patient-derived primary corneal keratocytes via homology-directed repair (HDR). To correct genetic defects in GCD patient cells, we designed a disease-specific guide RNA (gRNA) targeting the R124H mutation of TGFBI, which causes GCD type 2 (GCD2). An R124H mutation in primary human corneal keratocytes derived from a GCD2 patient was corrected by delivering a CRISPR plasmid expressing Cas9/gRNA and a single-stranded oligodeoxynucleotide HDR donor template in vitro. The gene correction efficiency was 20.6% in heterozygous cells and 41.3% in homozygous cells. No off-target effects were detected. These results reveal a new therapeutic strategy for GCD2; this method may also be applicable to other heredity corneal diseases

    Analysis of Area-Specific Expression Patterns of RORbeta, ER81 and Nurr1 mRNAs in Rat Neocortex by Double In Situ Hybridization and Cortical Box Method

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    BACKGROUND: The mammalian neocortex is subdivided into many areas, each of which exhibits distinctive lamina architecture. To investigate such area differences in detail, we chose three genes for comparative analyses, namely, RORbeta, ER81 and Nurr1, mRNAs of which have been reported to be mainly expressed in layers 4, 5 and 6, respectively. To analyze their qualitative and quantitative coexpression profiles in the rat neocortex, we used double in situ hybridization (ISH) histochemistry and cortical box method which we previously developed to integrate the data of different staining and individuals in a standard three-dimensional space. PRINCIPAL FINDINGS: Our new approach resulted in three main observations. First, the three genes showed unique area distribution patterns that are mostly complementary to one another. The patterns revealed by cortical box method matched well with the cytoarchitectonic areas defined by Nissl staining. Second, at single cell level, RORbeta and ER81 mRNAs were coexpressed in a subpopulation of layer 5 neurons, whereas Nurr1 and ER81 mRNAs were not colocalized. Third, principal component analysis showed that the order of hierarchical processing in the cortex correlates well with the expression profiles of these three genes. Based on this analysis, the dysgranular zone (DZ) in the somatosensory area was considered to exhibit a profile of a higher order area, which is consistent with previous proposal. CONCLUSIONS/SIGNIFICANCE: The tight relationship between the expression of the three layer specific genes and functional areas were revealed, demonstrating the usefulness of cortical box method in the study on the cerebral cortex. In particular, it allowed us to perform statistical evaluation and pattern matching, which would become important in interpreting the ever-increasing data of gene expression in the cortex
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