Tumor suppressor gene
    1.
    发明申请
    Tumor suppressor gene 失效
    肿瘤抑制基因

    公开(公告)号:US20070072231A1

    公开(公告)日:2007-03-29

    申请号:US11603619

    申请日:2006-11-22

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    摘要翻译: 从人睾丸cDNA文库中成功分离了编码参与细胞增殖控制的新蛋白质(人类Gros1-L和S)的全长cDNA。 还分离了编码人Gros1(小鼠Gros1-L和S)的小鼠同系物的全长cDNA。 外源性表达Gros1-L的细胞的集落形成活性显着降低,而表达Gros1反义RNA的细胞的集落形成活性显着增加。

    Tumor Suppressor Gene
    2.
    发明申请
    Tumor Suppressor Gene 审中-公开
    肿瘤抑制基因

    公开(公告)号:US20120156722A1

    公开(公告)日:2012-06-21

    申请号:US13401978

    申请日:2012-02-22

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    摘要翻译: 从人睾丸cDNA文库中成功分离了编码参与细胞增殖控制的新蛋白质(人类Gros1-L和S)的全长cDNA。 还分离了编码人Gros1(小鼠Gros1-L和S)的小鼠同系物的全长cDNA。 外源性表达Gros1-L的细胞的集落形成活性显着降低,而表达Gros1反义RNA的细胞的集落形成活性显着增加。

    Tumor suppressor gene
    3.
    发明授权
    Tumor suppressor gene 失效
    肿瘤抑制基因

    公开(公告)号:US08124733B2

    公开(公告)日:2012-02-28

    申请号:US12888572

    申请日:2010-09-23

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    摘要翻译: 从人睾丸cDNA文库中成功分离了编码参与细胞增殖控制的新蛋白质(人类Gros1-L和S)的全长cDNA。 还分离了编码人Gros1(小鼠Gros1-L和S)的小鼠同系物的全长cDNA。 外源性表达Gros1-L的细胞的集落形成活性显着降低,而表达Gros1反义RNA的细胞的集落形成活性显着增加。

    Tumor suppressor gene
    4.
    发明授权
    Tumor suppressor gene 失效
    肿瘤抑制基因

    公开(公告)号:US07825220B2

    公开(公告)日:2010-11-02

    申请号:US12626290

    申请日:2009-11-25

    IPC分类号: C07K16/00 C12N15/12 C12N15/00

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    摘要翻译: 从人睾丸cDNA文库中成功分离了编码参与细胞增殖控制的新蛋白质(人类Gros1-L和S)的全长cDNA。 还分离了编码人Gros1(小鼠Gros1-L和S)的小鼠同系物的全长cDNA。 外源性表达Gros1-L的细胞的集落形成活性显着降低,而表达Gros1反义RNA的细胞的集落形成活性显着增加。

    TUMOR SUPPRESSOR GENE
    5.
    发明申请
    TUMOR SUPPRESSOR GENE 失效
    肿瘤抑制基因

    公开(公告)号:US20110008913A1

    公开(公告)日:2011-01-13

    申请号:US12888572

    申请日:2010-09-23

    IPC分类号: G01N33/53 C07K14/435

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    摘要翻译: 从人睾丸cDNA文库中成功分离了编码参与细胞增殖控制的新蛋白质(人类Gros1-L和S)的全长cDNA。 还分离了编码人Gros1(小鼠Gros1-L和S)的小鼠同系物的全长cDNA。 外源性表达Gros1-L的细胞的集落形成活性显着降低,而表达Gros1反义RNA的细胞的集落形成活性显着增加。

    Tumor suppressor gene
    6.
    发明授权

    公开(公告)号:US07642070B2

    公开(公告)日:2010-01-05

    申请号:US11603619

    申请日:2006-11-22

    IPC分类号: C12N15/00

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    Tumor Suppressor Gene
    7.
    发明申请
    Tumor Suppressor Gene 失效
    肿瘤抑制基因

    公开(公告)号:US20100112591A1

    公开(公告)日:2010-05-06

    申请号:US12626290

    申请日:2009-11-25

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.

    摘要翻译: 从人睾丸cDNA文库中成功分离了编码参与细胞增殖控制的新蛋白质(人类Gros1-L和S)的全长cDNA。 还分离了编码人Gros1(小鼠Gros1-L和S)的小鼠同系物的全长cDNA。 外源性表达Gros1-L的细胞的集落形成活性显着降低,而表达Gros1反义RNA的细胞的集落形成活性显着增加。

    Tumor suppressor gene
    8.
    发明授权

    公开(公告)号:US07153935B2

    公开(公告)日:2006-12-26

    申请号:US10045815

    申请日:2001-10-26

    IPC分类号: C07K14/00 G01N33/53

    CPC分类号: C07K14/4703 A61K38/00

    摘要: A full-length cDNA encoding novel proteins involved in the control of cell proliferation (human Gros1-L and S) was successfully isolated from the human testis cDNA libraries. A full-length cDNA encoding the mouse homologues of the human Gros1 (mouse Gros1-L and S) was also isolated. The colony forming activity of cells exogenously expressing Gros1-L was significantly reduced, while that of cells expressing Gros1 antisense RNA was significantly increased.