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    • 3. 发明申请
    • METHOD FOR RATING SEVERITY OF PSORIASIS
    • 评估PSORIASIS的严重性的方法
    • WO2004034888A2
    • 2004-04-29
    • PCT/US2003/033218
    • 2003-10-20
    • ELLIS, Charles, N.
    • ELLIS, Charles, N.
    • A61B
    • A61B5/7264A61B5/441
    • Methods for rating the severity of psoriasis in a patient are provided. Such methods comprise assessing the percent of the patient’s body surface exhibiting signs of psoriasis, assessing the overall elevation, erythema, and scale of the patient’s psoriasis plaques, and classifying the severity of the patient’s psoriasis into at least four classes based upon the percent of the patient’s body surface exhibiting signs of psoriasis adjusted by the overall elevation, erythema and scale of the patient’s psoriasis plaques. In the present methods the weight given to one or more of the overall qualities of elevation, erythema or scale of the patient’s psoriasis plaques in classifying the severity of the patient’s psoriasis into a higher class is greater than the weight given to other of the overall qualities. A computer readable medium and system for practicing the present methods are also provided.
    • 提供了评估患者牛皮癣严重程度的方法。 这些方法包括评估患有牛皮癣症状的患者身体表面的百分比,评估患者牛皮癣斑块的总体高度,红斑和鳞屑以及将患者牛皮癣的严重程度分为至少四个等级,基于 患者的身体表面呈现由银屑病斑块的整体高程,红斑和鳞屑调节的银屑病征象。 在本方法中,给予患者牛皮癣斑块的高度,红斑或鳞屑的一个或多个整体质量的重量将患者牛皮癣的严重程度分类为更高级别的重量大于给予其他整体品质的重量 。 还提供了一种用于实施本方法的计算机可读介质和系统。
    • 7. 发明申请
    • WILD-TYPE RAS AS A CANCER THERAPEUTIC AGENT
    • 野生型作为癌症治疗剂
    • WO2003018755A2
    • 2003-03-06
    • PCT/US2002/026830
    • 2002-08-23
    • THE OHIO STATE UNIVERSITY RESEARCH FOUNDATIONYOU, MingWANG, YianZHANG, Zhongqui
    • YOU, MingWANG, YianZHANG, Zhongqui
    • C12N
    • A61K38/1709A61K48/00C12Q1/6886C12Q2600/156C12Q2600/158
    • Methods for inhibiting proliferation of a cell, particularly a cancer cell are provided. The method comprises increasing intracellular levels of one or more wild-type ras proteins in the cell. In one aspect, the method comprises introducing and expressing a nucleic molecule that encodes a wild-type ras protein in the cell. In another aspect, intracellular levels of one more ras proteins are increased by introducing one or more wild-type ras proteins into the cell. The present invention also relates to the therapeutic use of wild-type ras proteins or nucleic acids that encode one or more wild-type ras proteins in the treatment of tumors or cancer, or prophylactically to prevent formation of tumors or cancer. Methods of characterizing or evaluating cancer in a humans or other mammals are provided. In one embodiment, the method comprises assaying for a loss of function mutation in one or more endogenous ras alleles in the genome of tumor cells obtained from the subject. In another embodiment, the method comprises assaying for a loss of function mutation in one or more endogenous ras alleles and an activating mutation in one or more ras alleles in tumor cells obtained from the subject.
    • 提供了抑制细胞增殖的方法,特别是癌细胞。 该方法包括增加细胞中一种或多种野生型ras蛋白的细胞内水平。 一方面,该方法包括在细胞中引入和表达编码野生型ras蛋白的核酸分子。 另一方面,通过将一种或多种野生型ras蛋白引入细胞中来增加一种或多种ras蛋白的细胞内水平。 本发明还涉及编码一种或多种野生型ras蛋白质的野生型ras蛋白质或核酸在治疗肿瘤或癌症或预防性形成肿瘤或癌症中的治疗用途。 提供了表征或评估人类或其他哺乳动物中的癌症的方法。 在一个实施方案中,该方法包括测定从受试者获得的肿瘤细胞基因组中的一种或多种内源ras等位基因中的功能缺失突变。 在另一个实施方案中,所述方法包括测定从受试者获得的肿瘤细胞中一种或多种内源ras等位基因中的功能缺失突变和一种或多种ras等位基因中的激活突变。
    • 10. 发明申请
    • METHODS FOR EXPRESSING RNP PARTICLES IN EUKARYOTIC CELLS
    • 用于在核细胞中表达RNP颗粒的方法
    • WO2005123937A2
    • 2005-12-29
    • PCT/US2005/020893
    • 2005-06-14
    • THE UNIVERSITY OF TEXAS AT AUSTINCUI, XiaoxiaLAMBOWITZ, AlanSALDANHA, Roland
    • CUI, XiaoxiaLAMBOWITZ, AlanSALDANHA, Roland
    • C12P21/06
    • C12N15/63C12N15/85
    • Provided herein are nucleic acid constructs and methods for producing or enhancing the production of group II intron RNP particles in eukaryotic cells. The present methods comprise introducing at least one nucleic acid construct comprising a nucleic acid encoding a modified or wild type group II intron RNA and a wild-type or modified group II intron-encoded protein into the eukaryotic cell, and maintaining the cell under conditions that allow for expression of the group II intron RNA and the group II intron-encoded protein in the cell. The nucleic acid encoding the group II intron RNA is operably linked to an RNA polymerase I, an RNA polymerase II, or an RNA polymerase III promoter, and the nucleic acid encoding the group II intron-encoded protein is operably linked to an RNA polymerase II promoter. In certain embodiments, a subcellular localization signal is attached to the group II intron-encoded protein.
    • 本文提供了核酸构建体和用于在真核细胞中产生或增强II组内含子RNP颗粒的生产的方法。 本发明的方法包括将包含编码经修饰或野生型II组内含子RNA的核酸和野生型或修饰II型内含子编码蛋白质的至少一种核酸构建体引入真核细胞中,并将细胞维持在 允许在细胞中表达II组内含子RNA和II组内含子编码的蛋白质。 编码II组内含子RNA的核酸可操作地连接到RNA聚合酶I,RNA聚合酶II或RNA聚合酶III启动子,编码II组内含子编码蛋白的核酸可操作地连接到RNA聚合酶II 子。 在某些实施方案中,将亚细胞定位信号连接到II组内含子编码的蛋白质。