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    HUMAN HEPATITIS B VIRUS DNA
    1.
    发明公开
    HUMAN HEPATITIS B VIRUS DNA 失效
    DNS DES MENSCHLICHEN HEPATITIS B VIRUS

    公开(公告)号：EP0860505A1

    公开(公告)日：1998-08-26

    申请号：EP96935435.6

    申请日：1996-10-24

    申请人： OTSUKA PHARMACEUTICAL CO., LTD.

    发明人： KINOSHITA, Moritoshi ,  KATSURAGI, Kiyonori

    IPC分类号： C12N15/51 ,  C12Q1/68 ,  G01N27/26

    CPC分类号： C12Q1/706

    摘要： A pair of PCR primers designed so that the regions 1701 to 1794 of a human hepatitis B virus are selectively amplified and represented by, for example, SEQ ID NOS: 1 and 2; and DNA fragments (standards) consisting of the regions 1701 to 1794 of a human hepatitis B virus and represented by, for example, SEQ ID NOS: 3 to 8. The use of the same makes it possible to conduct genotyping of variations in the Pre-C region of a human hepatitis B virus genome and assaying of each genotype simultaneously therewith.

    摘要翻译： 设计成使得人乙型肝炎病毒的区域1701至1794被选择性扩增并由例如SEQ ID NO：1和2表示的一对PCR引物; 和由人乙型肝炎病毒的区域1701至1794组成并由例如SEQ ID NO：3至8表示的DNA片段（标准品）。使用该DNA片段（标准）可以进行Pre -C区域，并同时测定各基因型。

    PATHOLOGY DETERMINATION ASSISTANCE DEVICE, METHOD, PROGRAM AND STORAGE MEDIUM
    3.
    发明公开
    PATHOLOGY DETERMINATION ASSISTANCE DEVICE, METHOD, PROGRAM AND STORAGE MEDIUM 审中-公开
    病理学确定辅助装置，方法，程序和存储介质

    公开(公告)号：EP3219809A1

    公开(公告)日：2017-09-20

    申请号：EP14901111.6

    申请日：2014-09-03

    申请人： Otsuka Pharmaceutical Co., Ltd.

    发明人： KINOSHITA, Moritoshi ,  HIGASHIYAMA, Ryo ,  KOGA, Daisuke

    IPC分类号： C12Q1/68 ,  G06F17/30 ,  G06F19/28

    CPC分类号： G06F19/28 ,  C12Q1/68 ,  G06F17/30 ,  G06F17/30539

    摘要： An object of the present invention is to provide a device for assisting determination of pathology by displaying a list containing gene mutation information extracted from sequence data having gene sequence of a test subject, as well as various items of medical information regarding the gene mutation stored in public databases or the like, thereby specifying a pathogenic gene mutation of a test subject.
    The device for assisting determination of pathology of a polycystic kidney disease according to the present invention comprises an extraction means 21 for extracting gene mutation information in a region related to polycystic kidney disease using sequence data showing gene sequences of a test subject; an acquisition means 22 for acquiring, using the extracted gene mutation information, medical information corresponding to the extracted gene mutation from a plurality of databases in which gene mutation and medical information are associated with each other; and a list display means 23 for displaying a list containing the extracted gene mutation information and the obtained medical information.

    摘要翻译： 本发明的一个目的是提供一种用于通过显示包含从具有受试者的基因序列的序列数据中提取的基因突变信息的列表以及存储在受试者中的基因突变的各种医学信息的列表来辅助病理学确定的装置 公共数据库等，从而指定测试对象的致病性基因突变。 根据本发明的辅助诊断多囊肾病的病理的装置包括提取装置21，用于使用显示受试者的基因序列的序列数据提取与多囊肾病有关的区域中的基因突变信息; 获取装置22，用于使用所提取的基因突变信息从其中基因突变和医学信息彼此相关联的多个数据库中获取与所提取的基因突变相对应的医学信息; 和列表显示装置23，用于显示包含提取的基因突变信息和获得的医疗信息的列表。