Method of detecting cancer based on immune reaction to BORIS
    1.
    发明授权
    Method of detecting cancer based on immune reaction to BORIS 有权
    基于BORIS免疫反应检测癌症的方法

    公开(公告)号:US07785814B2

    公开(公告)日:2010-08-31

    申请号:US11575732

    申请日:2005-09-21

    IPC分类号: G01N33/574

    CPC分类号: G01N33/57407

    摘要: The invention provides a method of detecting a proliferative disease, such as a disease associated with the abnormal expression of BORIS, in a mammal comprising detecting antibodies to BORIS in a sample obtained from the mammal. The invention also provides BORIS polypeptides as well as compositions and kits comprising the BORIS polypeptides and methods of using the same. The invention further provides a method of inducing an immune response in a mammal using BORIS polypeptides.

    摘要翻译: 本发明提供了一种检测哺乳动物中增殖性疾病,例如与BORIS异常表达相关的疾病的方法,包括在从哺乳动物获得的样品中检测BORIS抗体。 本发明还提供BORIS多肽以及包含BORIS多肽的组合物和试剂盒及其使用方法。 本发明还提供了使用BORIS多肽在哺乳动物中诱导免疫应答的方法。

    METHODS FOR APPLICATION OF ENDOGENOUS OR EXOGENOUS STEM/PROGENITOR OR THEIR PROGENY FOR TREATMENT OF DISEASE
    2.
    发明申请
    METHODS FOR APPLICATION OF ENDOGENOUS OR EXOGENOUS STEM/PROGENITOR OR THEIR PROGENY FOR TREATMENT OF DISEASE 审中-公开
    应用内源性或外源性干扰素/原核生物或其治疗疾病的方法

    公开(公告)号:US20080206202A1

    公开(公告)日:2008-08-28

    申请号:US11927399

    申请日:2007-10-29

    IPC分类号: A61K48/00 C12N5/06

    摘要: We propose here that endogenous stem/progenitor cells of the developing or adult nervous system be genetically modified in situ, to express therapeutically advantageous gene products. Furthermore, we propose here that endogenous or other exogenous stem cells or their progeny be genetically modified when appropriate to express advantageous gene products (and/or modified through culture techniques), and that, if exogenously derived, they be transplanted into the ventricular system of the patient nervous system, the germinal zone of the ventricular system, into postmitotic regions of the CNS or other organs.

    摘要翻译: 我们在这里提出,发展中或成人神经系统的内源性干/祖细胞在原位转基因修饰,以表达治疗上有利的基因产物。 此外,我们在这里提出,内源或其他外源性干细胞或其后代在适当时进行遗传修饰以表达有利的基因产物(和/或通过培养技术修饰),并且如果外源性地将其移植到心室系统 患者神经系统,心室系统的生发区,进入CNS或其他器官的后状态区域。