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    OPERATING LEVER OF VEHICULAR SEAT
    3.
    发明申请
    OPERATING LEVER OF VEHICULAR SEAT 有权
    汽车座椅操作杆

    公开(公告)号：US20100207417A1

    公开(公告)日：2010-08-19

    申请号：US12439891

    申请日：2007-09-04

    申请人： Makoto Ito ,  Yoshihiro Ooishi ,  Tomohiro Muramatsu ,  Robert Day ,  Osamu Fujimoto

    发明人： Makoto Ito ,  Yoshihiro Ooishi ,  Tomohiro Muramatsu ,  Robert Day ,  Osamu Fujimoto

    IPC分类号： B60N2/30 ,  B60N2/44

    CPC分类号： B60N2/3011 ,  B60N2/3065 ,  B60N2/3075 ,  B60N2/919

    摘要： One aspect of the present invention can include an operating lever of a vehicular seat provided at a front face, an upper face, or a back face of a seat, including a seat cushion and a seat back, and a first lever and a second lever. The first lever and the second lever are axially supported pivotably to each other on one end sides in length directions. An other end side in the length direction of the first lever is axially supported pivotably to the seat and is connected to a lock mechanism capable of changing a state of an attitude of the seat. The other end side in the length direction of the second lever is formed as an operating portion. The attitude of the seat can be operated while bending the first lever in two stages around axial shafts on sides of both ends in the length direction of the first lever by operating an operating portion of the second lever in a direction of being remote from the seat.

    摘要翻译： 本发明的一个方面可以包括设置在座椅的前表面，上表面或背面的车辆用座椅的操作杆，其包括座垫和座椅靠背，以及第一杆和第二杆 。 第一杆和第二杆在长度方向上的一端侧可轴向地支撑。 第一杠杆的长度方向上的另一端侧可枢转地支撑在座椅上，并且连接到能够改变座椅状态的锁定机构。 第二杆的长度方向的另一端形成为操作部。 座椅的姿态可以通过在第二杆的远离座椅的方向上操作第二杆的操作部分而在第一杆的长度方向上的两端侧的轴向两端弯曲第一杆的同时进行操作 。

    File handling for naming conflicts
    4.
    发明申请
    File handling for naming conflicts 有权

    公开(公告)号：US20060271602A1

    公开(公告)日：2006-11-30

    申请号：US11136522

    申请日：2005-05-25

    申请人： Christopher Davis ,  David Johnson ,  Robert Day ,  Stephan Hoefnagels ,  Timothy McKee

    发明人： Christopher Davis ,  David Johnson ,  Robert Day ,  Stephan Hoefnagels ,  Timothy McKee

    IPC分类号： G06F17/30

    CPC分类号： G06F17/30067 ,  G06F17/30115 ,  G06F17/30123 ,  G06F17/30176

    摘要： A file operations engine is provided that manages many user interactions with their files via a computer system. The operation engine may provide a user with the option to keep both files that have a file name conflict. It may further permit the user to rename a file involved with a file name conflict. The operations engine may also automatically rename one of the files of a file name conflict by appending a character to a root of the filename. The character may include the lowest integer available for the root in a destination for the files. The operations engine may provide the option to keep both files as part of a pre-calculation of potential errors for a requested operation. The operations engine may place file name conflicts in an error queue and permit the user to select an option to keep both files after the conflict is encountered.

    Methods for identifying gibberellin responsive genes using cultured vegetable cells
    5.
    发明申请
    Methods for identifying gibberellin responsive genes using cultured vegetable cells 审中-公开
    使用培养的植物细胞鉴定赤霉素应答基因的方法

    公开(公告)号：US20050153288A1

    公开(公告)日：2005-07-14

    申请号：US10496530

    申请日：2002-12-20

    申请人： Eiichi Minami ,  Naoto Shibuya ,  Robert Day

    发明人： Eiichi Minami ,  Naoto Shibuya ,  Robert Day

    IPC分类号： A01H3/00 ,  C07K14/415 ,  C12Q1/68

    CPC分类号： C07K14/415

    摘要： To date, those skilled in the art have never considered that cultured plant cells respond to gibberellins. However, to comprehensively and conveniently identify and isolate gibberellin responsive genes, cultured cells, which are uniform and easy to handle, are appropriate. Considering the advantages of cultured cells, the present inventors developed methods for identifying and isolating gibberellin responsive genes using cultured cells. After pre-culturing cells in an auxin-free medium, they examined whether or not changes in gene expression could be detected. As a result, it was surprisingly revealed that changes in the expression of some genes could be detected after gibberellin treatment.

    摘要翻译： 迄今为止，本领域技术人员从未认为培养的植物细胞对赤霉素有反应。 然而，为了全面，方便地鉴定和分离赤霉素应答基因，培养的细胞是均匀且易于处理的。 考虑到培养细胞的优点，本发明人开发了使用培养细胞鉴定和分离赤霉素应答基因的方法。 在无生长素培养基中预培养细胞后，检查基因表达的变化是否被检测到。 结果令人吃惊地发现，赤霉素治疗后可以检测到某些基因的表达变化。

    Mammalian pro-hormone convertase
    8.
    发明授权
    Mammalian pro-hormone convertase 失效
    哺乳动物前体激素转化酶

    公开(公告)号：US5840529A

    公开(公告)日：1998-11-24

    申请号：US545562

    申请日：1995-10-19

    申请人： Nabil G. Seidah ,  Robert Day ,  Michel Chretien

    发明人： Nabil G. Seidah ,  Robert Day ,  Michel Chretien

    IPC分类号： G01N33/50 ,  A61K48/00 ,  C07K14/16 ,  C07K16/40 ,  C12N5/00 ,  C12N5/10 ,  C12N9/64 ,  C12N15/09 ,  C12N15/57 ,  C12P21/00 ,  C12Q1/68 ,  C12R1/91 ,  G01N33/53 ,  C07H21/04 ,  C07K14/00 ,  C12N15/63

    CPC分类号： C07K14/005 ,  C12N9/6454 ,  A61K48/00 ,  C12N2740/16122

    摘要： This invention relates to a novel and seventh member of the subtilisin-kexin family isolated from rat, which has been named rPC7. The rat spleen cDNA has been totally sequenced. A shorter DNA sequence has been obtained for human, which corresponds to a portion of the catalytic region of a human pro-hormone convertase corresponding to the rat pro-hormone convertase. PC7 clearly distinguishes from the other mammalian members of the subtilisin-kexin family. Its tissue distribution is ubiquitous, but its presence is particularly remarkable in lymphoid tissues. It is present in LoVo cells that are able to cleave the HIV gp160 protein into active gp120/gp41 proteins and that are deficient in other effective pro-hormone convertases known up to date. Therefore, it is proposed that PC7 is a good candidate as a maturation enzyme responsible for the conversion of HIV gp160 protein in target CD.sup.+4 cells.

    摘要翻译： 本发明涉及从大鼠中分离的枯草杆菌蛋白酶-Kexin家族的新颖和第七个成员，其被命名为rPC7。 大鼠脾脏cDNA已经完全测序。 人类已经获得了较短的DNA序列，其对应于对应于大鼠前体激素转化酶的人类前体激素转化酶的一部分催化区域。 PC7明显区别于枯草杆菌蛋白酶-Kexin家族的其他哺乳动物成员。 其组织分布普遍存在，但其淋巴组织中的存在特别显着。 它存在于能够将HIV gp160蛋白切割成活性gp120 / gp41蛋白质的LoVo细胞中，并且缺乏其他已知的有效的促激素转化酶。 因此，建议PC7作为负责在目标CD + 4细胞中转染HIV gp160蛋白质的成熟酶的良好候选物。