288 research outputs found

    日本住人の低いHAV抗体保有率はHAV感染のアウトブレイクを惹起させる高い可能性を有す

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    広島大学(Hiroshima University)博士(医学)Doctor of Philosophy in Medical Sciencedoctora

    Unc93B1によるToll-like receptor(TLR)7及びTLR9の応答制御機構の解析

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    学位の種別: 課程博士審査委員会委員 : (主査)東京大学特任教授 谷口 維紹, 東京大学教授 川口 寧, 東京大学教授 山本 一彦, 東京大学教授 北村 俊雄, 東京大学准教授 新田 剛University of Tokyo(東京大学

    Configurational studies of complexes of tea catechins with caffeine and various cyclodextrins.

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    A suspension of an equimolecular amount of ENT-gallocatechin-3-O-gallate ( ENTGCg) and caffeine in water afforded two kinds of crystals, which were 1 : 2 and 2 : 2 complexes of ENTGCg and caffeine. The stereochemical structures and intermolecular interactions between ENTGCg and caffeine were determined by X-ray crystallographic analysis. The crystal structure of ENTGCg was determined and compared with those of the 1 : 2 and 2 : 2 complexes. Epigallocatechin-3-O-gallate (EGCg) formed a 1 : 1 complex with β-cyclodextrin (CD), in which the aromatic A ring and a part of the heterocyclic C ring were included from the wide secondary hydroxyl group side of the β-CD cavity in aqueous solution, while the B rings and 3-O-gallate groups (B\u27 rings) were left outside the cavity. In contrast, ENTGCg formed a 1 : 2 complex with β-CD, in which the aromatic A and B rings of ENTGCg were included by two molecules of β-CD.A suspension of an equimolecular amount of ENT-gallocatechin-3-O-gallate ( ENTGCg) and caffeine in water afforded two kinds of crystals, which were 1 : 2 and 2 : 2 complexes of ENTGCg and caffeine. The stereochemical structures and intermolecular interactions between ENTGCg and caffeine were determined by X-ray crystallographic analysis. The crystal structure of ENTGCg was determined and compared with those of the 1 : 2 and 2 : 2 complexes. Epigallocatechin-3-O-gallate (EGCg) formed a 1 : 1 complex with β-cyclodextrin (CD), in which the aromatic A ring and a part of the heterocyclic C ring were included from the wide secondary hydroxyl group side of the β-CD cavity in aqueous solution, while the B rings and 3-O-gallate groups (B\u27 rings) were left outside the cavity. In contrast, ENTGCg formed a 1 : 2 complex with β-CD, in which the aromatic A and B rings of ENTGCg were included by two molecules of β-CD

    Liquid Biopsy Revealed HBOC Pedigree and Led to Medical Management Among the Relatives

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    A hereditary breast and ovarian cancer (HBOC) pedigree was detected via liquid biopsy, and cancer prevention was initiated for the patient’s daughter, after receiving a definitive result from BRCA genetic testing. A 48-yearold woman with ovarian cancer was administered precision medicine, which used cell-free DNA from plasma. The results revealed a pathogenic variant of BRCA1 as a presumed germline pathogenic mutation. We confirmed the germline pathological variant BRCA1 c.81-1G> A and suggested treatment with a PARP inhibitor. One of her three children had the variant, was diagnosed as an unaffected pathogenic variant carrier, and was advised to initiate surveillance

    Suppression of HBV replication by the expression of nickase-and nuclease dead-Cas9

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    Kurihara, T., Fukuhara, T., Ono, C. et al. Suppression of HBV replication by the expression of nickase- and nuclease dead-Cas9. Sci Rep 7, 6122 (2017). https://doi.org/10.1038/s41598-017-05905-

    Efficient Genome Editing in Apple Using a CRISPR/Cas9 system

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    Genome editing is a powerful technique for genome modification in molecular research and crop breeding, and has the great advantage of imparting novel desired traits to genetic resources. However, the genome editing of fruit tree plantlets remains to be established. In this study, we describe induction of a targeted gene mutation in the endogenous apple phytoene desaturase (PDS) gene using the CRISPR/Cas9 system. Four guide RNAs (gRNAs) were designed and stably transformed with Cas9 separately in apple. Clear and partial albino phenotypes were observed in 31.8% of regenerated plantlets for one gRNA, and bi-allelic mutations in apple PDS were confirmed by DNA sequencing. In addition, an 18-bp gRNA also induced a targeted mutation. These CRIPSR/Cas9 induced-mutations in the apple genome suggest activation of the NHEJ pathway, but with some involvement also of the HR pathway. Our results demonstrate that genome editing can be practically applied to modify the apple genome
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