Novel Gene Disruptions, Compositions and Methods Relating Thereto
    17.
    发明申请
    Novel Gene Disruptions, Compositions and Methods Relating Thereto 失效
    新型基因中断,组成和方法

    公开(公告)号:US20080160034A1

    公开(公告)日:2008-07-03

    申请号:US11572702

    申请日:2005-08-23

    摘要: The present invention relates to transgenic animals, as well as compositions and methods relating to the characterization of gene function. Specifically, the present invention provides transgenic mice comprising disruptions in PRO196, PRO217, PRO231, PRO236, PRO245, PRO246, PRO258, PRO287, PRO328, PRO344, PRO357, PRO526, PRO724, PRO731, PRO732, PRO1003, PRO1104, PRO1151, PRO1244, PRO1298, PRO1313, PRO1570, PRO1886, PRO1891, PRO4409, PRO5725, PRO5994, PRO6097, PRO7425, PRO10102, PRO10282, PRO61709 or PRO779 genes. Such in vivo studies and characterizations may provide valuable identification and discovery of therapeutics and/or treatments useful in the prevention, amelioration or correction of diseases or dysfunctions associated with gene disruptions such as neurological disorders; cardiovascular, endothelial or angiogenic disorders; eye abnormalities; immunological disorders; oncological disorders; bone metabolic abnormalities or disorders; lipid metabolic disorders; or developmental abnormalities.

    摘要翻译: 本发明涉及转基因动物,以及与基因功能表征相关的组合物和方法。 具体地说,本发明提供转基因小鼠,其包括PRO196,PRO217,PRO231,PRO236,PRO245,PRO246,PRO258,PRO287,PRO328,PRO344,PRO357,PRO526,PRO724,PRO731,PRO732,PRO1003,PRO1104,PRO1151,PRO1244,PRO1298中的中断 ,PRO1313,PRO1570,PRO1886,PRO1891,PRO4409,PRO5725,PRO5994,PRO6097,PRO7425,PRO10102,PRO10282,PRO61709或PRO779基因。 这样的体内研究和表征可以提供有用的识别和发现治疗和/或治疗用于预防,改善或矫正与基因中断相关的疾病或功能障碍如神经障碍; 心血管,内皮或血管生成障碍; 眼睛异常; 免疫学障碍; 肿瘤疾病; 骨代谢异常或障碍; 脂代谢紊乱 或发育异常。

    Gene disruptions, compositions and methods relating thereto
    18.
    发明授权
    Gene disruptions, compositions and methods relating thereto 失效
    基因破坏,组合物和方法

    公开(公告)号:US07858843B2

    公开(公告)日:2010-12-28

    申请号:US11814361

    申请日:2006-05-18

    IPC分类号: G01N33/00 C12N5/06 C12Q1/02

    摘要: The present invention relates to transgenic animals, as well as compositions and methods relating to the characterization of gene function. Specifically, the present invention provides transgenic mice comprising disruptions in PRO69122, PRO204, PRO214, PRO222, PRO234, PRO265, PRO309, PRO332, PRO342, PRO356, PRO540, PRO618, PRO944, PRO994, PRO1079, PRO1110, PRO1122, PRO1138, PRO1190, PRO1272, PRO1286, PRO1295, PRO1309, PRO1316, PRO1383, PRO1384, PRO1431, PRO1434, PRO1475, PRO1481, PRO1568, PRO1573, PRO1599, PRO1604, PRO1605, PRO1693, PRO1753, PRO1755, PRO1777, PRO1788, PRO1864, PRO1925, PRO1926, PRO3566, PRO4330, PRO4423, PRO36935, PRO4977, PRO4979, PRO4980, PRO4981, PRO5801, PRO5995, PRO6001, PRO6095, PRO6182, PRO7170, PRO7171, PRO7436, PRO9912, PRO9917, PRO37337, PRO37496, PRO19646, PRO21718, PRO19820, PRO21201, PRO20026, PRO20110, PRO23203 or PRO35250 genes. Such in vivo studies and characterizations may provide valuable identification and discovery of therapeutics and/or treatments useful in the prevention, amelioration or correction of diseases or dysfunctions associated with gene disruptions such as neurological disorders; cardiovascular, endothelial or angiogenic disorders; eye abnormalities; immunological disorders; oncological disorders; bone metabolic abnormalities or disorders; lipid metabolic disorders; or developmental abnormalities.

    摘要翻译: 本发明涉及转基因动物,以及与基因功能表征相关的组合物和方法。 具体地,本发明提供转基因小鼠,其包括PRO69122,PRO204,PRO214,PRO222,PRO234,PRO265,PRO309,PRO332,PRO342,PRO356,PRO540,PRO618,PRO944,PRO994,PRO1079,PRO1110,PRO1122,PRO1138,PRO1190,PRO1272中的中断 ,PRO1286,PRO1295,PRO1309,PRO1316,PRO1383,PRO1384,PRO1431,PRO1434,PRO1475,PRO1481,PRO1568,PRO1573,PRO1599,PRO1604,PRO1605,PRO1693,PRO1753,PRO1755,PRO1777,PRO1788,PRO1864,PRO1925,PRO1926,PRO3566,PRO4330 ,PRO4423,PRO36935,PRO4977,PRO4979,PRO4980,PRO4981,PRO5801,PRO5995,PRO6001,PRO6095,PRO6182,PRO7170,PRO7171,PRO7436,PRO9912,PRO9917,PRO37337,PRO37496,PRO19646,PRO21718,PRO19820,PRO21201,PRO20026,PRO20110,PRO23203 或PRO35250基因。 这样的体内研究和表征可以提供有用的识别和发现治疗和/或治疗用于预防,改善或矫正与基因中断相关的疾病或功能障碍如神经障碍; 心血管,内皮或血管生成障碍; 眼睛异常; 免疫学障碍; 肿瘤疾病; 骨代谢异常或障碍; 脂代谢紊乱 或发育异常。