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    • 1. 发明申请
    • AN ELECTRONIC AUTOROUTING NAVIGATION SYSTEM FOR VISUALLY IMPAIRED PERSONS
    • 用于视觉受损人员的电子自动导航系统
    • WO1998008108A1
    • 1998-02-26
    • PCT/US1997014525
    • 1997-08-19
    • BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEMHANCOCK, Michael, B.
    • BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
    • G01S03/02
    • G01C21/20G01S1/70
    • The present invention is an autorouting navigation system (100) for directing one or more visually impaired persons to a physical location. The present invention includes a portable autonavigation unit (100) that includes an input device (106) for selecting a target location corresponding to a physical location of a plurality of location beacons, a receiver (101) configured to receive signals from location beacons, a memory (103) storing information correlating the locations of the location beacons, and an output device (104) for communicating with the user. A microcontroller (105) or microprocessor under program control processes the signals received from the location beacons, analyzes those signals and correlation data, and determines a routing path from the user's present position to the target location. The microcontroller (105) may also provide an indication, such as an audible sound, to the user of whether or not the user is following the routing path to the target location.
    • 本发明是一种用于将一个或多个视障人员引导到物理位置的自动布线导航系统(100)。 本发明包括便携式自动导航单元(100),其包括用于选择对应于多个位置信标的物理位置的目标位置的输入设备(106),被配置为从位置信标接收信号的接收机(101) 存储器(103)存储与位置信标的位置相关的信息,以及用于与用户通信的输出设备(104)。 在程序控制下的微控制器(105)或微处理器处理从位置信标接收到的信号,分析这些信号和相关数据,并且确定从用户的当前位置到目标位置的路由路径。 微控制器(105)还可以向用户提供关于用户是否遵循到目标位置的路由路径的指示,例如可听见的声音。
    • 3. 发明申请
    • PROTEINS AND COMPOSITIONS FOR MODULATING MITOSIS
    • 调理麻醉剂的蛋白质和组合物
    • WO1998045433A1
    • 1998-10-15
    • PCT/US1998006727
    • 1998-04-03
    • BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEMCLARK, Gary, M.ALLRED, D., CraigHILSENBECK, Susan, G.CHAMNESS, Gary, C.OSBORNE, C., Kent
    • BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
    • C12N15/12
    • C07K14/47A61K38/00
    • The protein encoded by the human gene HEC ( h ighly e xpressed in c ancer) contains a long series of leucine heptad repeats and appears to be crucial for normal mitosis. HEC localizes to the nuclei of interphase cells and redistributes to centromeres during M phase. Ectopic expression of a mutant HEC containing only the heptad repeats results in the inability of cells to divide more than once. Inactivation of HEC results in disordered sister chromatid alignment and separation, as well as in the formation of nonviable cells with multiple, fragmented micronuclei. HEC interacts through its leucine heptad repeats with several proteins involved in mitosis, including nek2, sb1.8, and two different regulatory subunits of the 26S proteasome, MSS1 and p45. These biochemical properties of HEC suggest its potential roles in modulating proteins important for spindle attachment to kinetochores, sister chromatid movement, and M phase progression.
    • 由人类基因HEC(高表达胰岛素)表达的蛋白质编码的蛋白质含有长序列的亮氨酸七肽重复序列,似乎是 对正常有丝分裂至关重要 HEC定位于相间细胞核,并在M期期间重新分布至着丝粒。 仅含有七重复重复的突变体HEC的异位表达导致细胞不能分裂多于一次。 HEC的失活导致无序的姐妹染色单体比对和分离,以及形成具有多个片段微核的不可维持细胞。 HEC通过其亮氨酸七肽重复与涉及有丝分裂的几种蛋白质相互作用,包括nek2,sb1.8和26S蛋白酶体,MSS1和p45的两个不同调节亚基。 HEC的这些生物化学性质表明其在调节重要的心脏附着到动粒细胞,姐妹染色单体运动和M期进展中的蛋白质的潜在作用。
    • 5. 发明申请
    • PROTEINS AND COMPOSITIONS FOR MODULATING MITOSIS
    • 调理麻醉剂的蛋白质和组合物
    • WO1998027994A1
    • 1998-07-02
    • PCT/US1997023385
    • 1997-12-18
    • BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
    • BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEMLEE, Wen-HwaCHEN, YumayRILEY, Daniel, J.CHEN, Phang-Lang
    • A61K38/08
    • C07K14/4702
    • The protein encoded by the human gene HEC( h ighly e xpressed in c ancer) contains a long series of leucine heptad repeats and appears to be crucial for normal mitosis. HEC localizes to the nuclei of interphase cells and redistributes to centromeres during M phase. Ectopic expression of a mutant HEC containing only the heptad repeats results in the inability of cells to divide more than once. Inactivation of HEC results in disordered sister chromatid alignment and separation, as well as in the formation of non viable cells with multiple, fragmented micronuclei. HEC interacts through its leucine heptad repeats with several proteins involved in mitosis, including nek2, sb1.8, and two different regulatory subunits of the 26S proteasome, MSS1 and p45. These biochemical properties of HEC suggest its potential roles in modulating proteins important for spindle attachment to kinetochores, sister chromatic movement, and M phase progression.
    • 由人类基因HEC(高表达胰岛素)表达的蛋白质编码的蛋白质含有长序列的亮氨酸七肽重复序列,似乎是 对正常有丝分裂至关重要 HEC定位于相间细胞核,并在M期期间重新分布至着丝粒。 仅含有七重复重复的突变体HEC的异位表达导致细胞不能分裂多于一次。 HEC的失活导致无序的姐妹染色单体比对和分离,以及形成具有多个片段微核的非活细胞。 HEC通过其亮氨酸七肽重复与涉及有丝分裂的几种蛋白质相互作用,包括nek2,sb1.8和26S蛋白酶体,MSS1和p45的两个不同调节亚基。 HEC的这些生物化学性质表明其在调节重要的心脏附着到动粒细胞,姐妹色彩运动和M期进展中的蛋白质的潜在作用。