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    • 1. 发明授权
    • Methods of decreasing the accumulation of extracellular matrix associated with glomerulonephritis with anti-TGF-β-specific antibodies
    • 用抗TGF-β特异性抗体降低与肾小球肾炎相关的细胞外基质积累的方法
    • US07214375B1
    • 2007-05-08
    • US08349479
    • 1994-12-02
    • Wayne A. BorderErkki I. Ruoslahti
    • Wayne A. BorderErkki I. Ruoslahti
    • A61K39/395C07K16/24
    • C07K16/22A61K2039/505
    • The present invention provides a method for treating or arresting the progress of pathologies characterized by an accumulation of extracellular matrix components by providing an agent to suppress the activity of transforming growth factor β (TGF-β) a peptide growth factor which is anabolic and leads to fibrosis and angiogenesis. In one embodiment, such agent is anti-TGF-β antibody. Pathologies which can be so treated include, but are not limited to, glomerulonephritis, adult respiratory distress syndrome and cirrhosis of the liver. The invention further provides a method for the diagnosis of pathologies, or incipient pathologies, which are characterized by the accumulation of extracellular matrix components in tissues by determining the levels of TGF-β in the tissues, a high level being indicative of such pathologies.
    • 本发明提供了一种通过提供抑制转化生长因子β(TGF-β)的活性的药剂来治疗或阻止细胞外基质成分积累的病态的方法,所述肽生长因子是合成代谢并导致 纤维化和血管生成。 在一个实施方案中,这种试剂是抗TGF-β抗体。 可以如此治疗的病理包括但不限于肾小球性肾炎,成人呼吸窘迫综合征和肝硬化。 本发明还提供了用于诊断病理学或初期病理学的方法,其特征在于通过测定组织中TGF-β的水平,组织中的细胞外基质组分的积累指示这种病理学的高水平。
    • 5. 发明授权
    • Fibronectin Type III polypeptides
    • 纤连蛋白III型多肽
    • US5837813A
    • 1998-11-17
    • US460421
    • 1995-06-01
    • Erkki I. RuoslahtiAlex Morla
    • Erkki I. RuoslahtiAlex Morla
    • A61K38/00C07K14/78A61K38/39
    • C07K14/78A61K38/00
    • The present invention provides fibronectin self-assembly sites. The invention provides a set of polypeptides derived from the first type III repeat of fibronectin which contain a fibronectin-fibronectin binding site. These polypeptides have been used to obtain a second set of polypeptides derived from the C-terminal type I repeats which contain a second fibronectin-fibronectin binding site which interacts with the first type III repeat of fibronectin. These polypeptides are capable of inhibiting fibronectin matrix assembly by interfering with fibronectin-fibronectin binding. These polypeptides are also capable of enhancing fibronectin matrix assembly and inducing disulfide cross-linking of fibronectin molecules in vitro. In addition, these polypeptides are capable of inhibiting migration of tumor cells. The polypeptides of the present invention have a number of related uses as well.
    • 本发明提供纤连蛋白自组装位点。 本发明提供一组衍生自含有纤连蛋白 - 纤连蛋白结合位点的纤连蛋白的第一III型重复序列的多肽。 已经使用这些多肽获得源自C末端I型重复序列的第二组多肽,其含有与纤连蛋白的第一III型重复相互作用的第二纤连蛋白 - 纤连蛋白结合位点。 这些多肽能够通过干扰纤连蛋白 - 纤连蛋白结合来抑制纤连蛋白基质组装。 这些多肽还能够体外增强纤连蛋白基质的组装和诱导纤连蛋白分子的二硫键交联。 此外,这些多肽能够抑制肿瘤细胞的迁移。 本发明的多肽也具有许多相关用途。