USE OF ICAM-1 FOR PREVENTION OR TREATMENT OF NEUROLOGICAL DISEASES
    1.
    发明申请
    USE OF ICAM-1 FOR PREVENTION OR TREATMENT OF NEUROLOGICAL DISEASES 有权
    使用ICAM-1预防或治疗神经病

    公开(公告)号:US20120196809A1

    公开(公告)日:2012-08-02

    申请号:US13365022

    申请日:2012-02-02

    CPC分类号: A61K38/1774

    摘要: The present invention relates to a pharmaceutical composition for the prevention or treatment of neurological disorders, comprising an ICAM-1 (intercellular adhesion molecule-1) protein, or a fragment or a variant thereof as an active ingredient, which can increase the expression of neprilysin to remove amyloid-beta (Aβ), a cause of dementia, and is thus useful in preventing or treating a neurological disease including Alzheimer's disease.

    摘要翻译: 本发明涉及一种用于预防或治疗神经系统疾病的药物组合物,其包含作为活性成分的ICAM-1(细胞间粘附分子-1)蛋白或其片段或变体,其可以增加内皮素的表达 去除淀粉样蛋白β(A&bgr),是痴呆的一个原因,因此可用于预防或治疗包括阿尔茨海默病在内的神经疾病。

    COMPOSITION FOR THE DIAGNOSIS, PREVENTION OR TREATMENT OF DISEASES RELATED TO CELLS EXPRESSING IL-8 OR GRO-ALPHA, COMPRISING UCB-MSCS
    2.
    发明申请
    COMPOSITION FOR THE DIAGNOSIS, PREVENTION OR TREATMENT OF DISEASES RELATED TO CELLS EXPRESSING IL-8 OR GRO-ALPHA, COMPRISING UCB-MSCS 有权
    用于诊断,预防或治疗与表达UC-8或GRO-ALPHA的细胞相关的疾病的组合物,包括UCB-MSCS

    公开(公告)号:US20100143261A1

    公开(公告)日:2010-06-10

    申请号:US12633622

    申请日:2009-12-08

    摘要: Provided is a gene therapy composition for transferring one of a therapeutical gene, a maker gene, or a mixture thereof to a cell that expresses interleukin-8(IL-8) or GRO-α and induces tropism of mesenchymal stem cells isolated from umbilical cord blood and/or the mesenchymal stem cells expanded from said mesenchymal stem cells (UCB-MSCs), wherein the cell-treating composition includes UCB-MSCs. Provided is a composition for treating disease related to a cell expressing IL-8 or GRO-α, that is, a brain tumor in gene therapy, by using UCB-MSCs. Provided is a composition or kit for diagnosing brain tumors, preventing brain tumors, treating brain tumors, or monitoring brain tumor treatment progression by using UCB-MSCs.

    摘要翻译: 提供了将治疗基因,制造者基因或其混合物中的一种转移至表达白细胞介素-8(IL-8)或GRO-α的细胞的基因治疗组合物,并诱导从脐带分离的间充质干细胞的嗜性 血液和/或从所述间充质干细胞(UCB-MSC)扩增的间充质干细胞,其中细胞处理组合物包括UCB-MSC。 提供了通过使用UCB-MSC来治疗与表达IL-8或GRO-α的细胞相关的疾病,即基因治疗中的脑肿瘤的组合物。 提供了用于诊断脑肿瘤,预防脑肿瘤,治疗脑肿瘤或通过使用UCB-MSC监测脑肿瘤治疗进展的组合物或试剂盒。

    SISP-1, A NOVEL P53 TARGET GENE AND USE THEREOF
    3.
    发明申请
    SISP-1, A NOVEL P53 TARGET GENE AND USE THEREOF 有权
    SISP-1,新型P53靶基因及其用途

    公开(公告)号:US20070237745A1

    公开(公告)日:2007-10-11

    申请号:US11679803

    申请日:2007-02-27

    申请人: Yoon-Sun YANG

    发明人: Yoon-Sun YANG

    摘要: The present invention relates to a novel p53 target gene SISP-1 (Stress induced Secreted Protein 1) and a SISP-1 protein encoded by the gene. The SISP-1 protein of the present invention induces apoptosis by interaction with p53. The present invention provides the use of the gene/protein associated with treating abnormal apoptosis such as tumor.

    摘要翻译: 本发明涉及新型p53靶基因SISP-1(应激诱导分泌蛋白1)和由该基因编码的SISP-1蛋白。 本发明的SISP-1蛋白通过与p53的相互作用诱导凋亡。 本发明提供与治疗异常细胞凋亡相关的基因/蛋白质如肿瘤的用途。