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    • 2. 发明申请
    • COMPOUND PROFILING METHOD
    • 化合物分析方法
    • US20090004171A1
    • 2009-01-01
    • US12101719
    • 2008-04-11
    • Masato MiyakeYoshiji Fujita
    • Masato MiyakeYoshiji Fujita
    • A61K38/44C12Q1/68C40B30/06A61P35/00C12M1/34
    • G01N33/5026C12Q1/6886C12Q2600/178G01N33/5011G16B5/00
    • The present invention provides a method for deriving an upstream or downstream component of a component necessary for phenotypic alteration of a living organism, the method comprising the steps of: specifying a pathway of interest related to the phenotypic alteration and a reference pathway different from the pathway of interest, and specifying a stimulant of interest and a reference stimulant which respectively stimulate the pathway of interest and the reference pathway; giving the stimulant of interest to the living organism to identify a collection of components of interest necessary for the phenotypic alteration; giving the reference stimulant to the living organism to identify a collection of reference components necessary for the phenotypic alteration; calculating an intersection between the collections of the components of interest and the reference components; and calculating a differential collection by subtracting the intersection from the collection of components of interest.
    • 本发明提供了一种用于衍生生物体表型改变所必需的组分的上游或下游组分的方法,所述方法包括以下步骤:指定与所述表型改变相关的感兴趣途径和不同于所述途径的参考途径 并且指定分别刺激感兴趣途径和参考途径的兴趣兴奋剂和参考刺激物; 给予活体有兴趣的兴奋剂,以确定表型改变所必需的组成部分的集合; 给生物体提供参考刺激物,以确定表型改变所必需的参考组分的集合; 计算感兴趣组件的集合和参考组件之间的交集; 以及通过从所述关注部件的收集中减去所述交叉点来计算差分收集。
    • 5. 发明申请
    • COMPOUND PROFILING METHOD
    • 化合物分析方法
    • US20100210708A1
    • 2010-08-19
    • US12595604
    • 2008-04-07
    • Masato MiyakeYoshiji Fujita
    • Masato MiyakeYoshiji Fujita
    • A61K31/7088C12Q1/02C12Q1/68C40B30/06
    • G01N33/5026C12Q1/6886C12Q2600/178G01N33/5011G16B5/00
    • The present invention provides a method for deriving an upstream or downstream component of a component necessary for phenotypic alteration of a living organism, the method comprising the steps of: specifying a pathway of interest related to the phenotypic alteration and a reference pathway different from the pathway of interest, and specifying a stimulant of interest and a reference stimulant which respectively stimulate the pathway of interest and the reference pathway; giving the stimulant of interest to the living organism to identify a collection of components of interest necessary for the phenotypic alteration; giving the reference stimulant to the living organism to identify a collection of reference components necessary for the phenotypic alteration; calculating an intersection between the collections of the components of interest and the reference components; and calculating a differential collection by subtracting the intersection from the collection of components of interest.
    • 本发明提供了一种用于衍生生物体表型改变所必需的组分的上游或下游组分的方法,所述方法包括以下步骤:指定与所述表型改变相关的感兴趣途径和不同于所述途径的参考途径 并且指定分别刺激感兴趣途径和参考途径的兴趣兴奋剂和参考刺激物; 给予活体有兴趣的兴奋剂,以确定表型改变所必需的组成部分的集合; 给生物体提供参考刺激物,以确定表型改变所必需的参考组分的集合; 计算感兴趣组件的集合和参考组件之间的交集; 以及通过从所述关注部件的收集中减去所述交叉点来计算差分收集。
    • 8. 发明申请
    • Digital cell
    • 数字电池
    • US20060253258A1
    • 2006-11-09
    • US10562469
    • 2004-06-25
    • Masato Miyake
    • Masato Miyake
    • G06F19/00C12Q1/00C12Q1/68
    • G01N33/5005C12M41/48
    • It is intended to provide a method and system for carrying out data production with respect to the actual status of cells as a profile. It is also intended to provide a system and method for presenting time-lapse and/or real-time information of cell interior directly, or as it is, from the viewpoint of a complex system. It is further intended to provide a method of presenting a digital cell. Thus, there is provided a method of producing profile data relating to cell information, comprising the step (a) of arranging cells in an immobilized form on a support and the step (b) of monitoring over time biological factors on or inside the cells or an aggregate thereof, thereby producing profile data for the cells. Furthermore, there is provided a method of producing a digital cell, comprising procuring experimental data by the use of the above method.
    • 旨在提供一种用于执行关于作为简档的单元的实际状态的数据生成的方法和系统。 本发明还旨在提供一种从复杂系统的观点直接或者原样呈现小区内部的延时和/或实时信息的系统和方法。 还旨在提供呈现数字单元的方法。 因此,提供了一种产生与细胞信息相关的分布数据的方法,其包括将固定化形式的细胞排列在支持体上的步骤(a)和步骤(b) 其聚合,从而产生细胞的轮廓数据。 此外,提供了一种制造数字单元的方法,包括通过使用上述方法获得实验数据。
    • 10. 发明授权
    • Bearing seal
    • 轴承密封
    • US07946592B2
    • 2011-05-24
    • US11666516
    • 2005-11-01
    • Hiroshi YamamotoJun MaruyamaMasato MiyakeKazuhiro HatakeToru Matsuyama
    • Hiroshi YamamotoJun MaruyamaMasato MiyakeKazuhiro HatakeToru Matsuyama
    • F16J15/32
    • F16J15/3224
    • A bearing seal includes: a ring-shaped outer seal portion; a ring-shaped inner seal portion provided inside the outer seal portion; a connecting portion for connecting the inner seal portion and the outer seal portion; and a ring-shaped rigid portion provided at the connecting portion. The outer seal portion, the inner seal portion, and the connecting portion are integrally formed of the same material consisting of an elastic material. The inner seal portion has rigidity higher than that of the outer seal portion, and has a ring-shaped seal surface gradually approaching a ring center axis of the inner seal portion while extending from a ring-shaped base end side connected to the connecting portion toward a distal end side.The inner seal portion is formed in a tapered cylindrical shape having the ring-shaped seal surface on an inner peripheral surface thereof, and has a thickness which gradually decreases from the base end side toward the distal end side. The inner seal portion includes only one inner seal portion.
    • 轴承密封件包括:环形外密封部分; 设置在所述外密封部内的环状的内密封部; 用于连接内部密封部分和外部密封部分的连接部分; 以及设置在连接部分处的环形刚性部分。 外密封部分,内密封部分和连接部分由与弹性材料相同的材料一体地形成。 内密封部具有比外密封部高的刚性,并且从连接到连接部的环状基端侧延伸的环状密封面逐渐接近内密封部的环心轴线, 远端侧。 内密封部形成为在其内周面上具有环状密封面的锥形圆筒形状,并且具有从基端侧朝向前端侧逐渐减小的厚度。 内密封部仅包括一个内密封部。