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Diagnosis and Treatment of glaucoma and methods to discover new therapeutic agents based on the Signalling Pathway of Wnt / Ca2 -

机译:青光眼的诊断和治疗以及基于Wnt / Ca2-的信号传导途径发现新治疗剂的方法-

摘要

Claim 1: a method to Diagnose glaucoma in a patient, the method comprising the following steps: (a) obtaining a sample of the patient; or (b) to detect the level of bioactivity component of Wnt / Ca2 + Pathway, a product of Frizzled Related Protein gene The Wnt / Ca2 + Pathway.A FRP or via the Wnt / Ca2 + and (c) comparing the level of bioactivity or component of the Wnt / Ca2 + Pathway, Gene product of Frizzled Related Protein or FRP of the Wnt / Ca2 + level in a normal Sample, where a level of bioactivity Component or Aberrant The Path of The Wnt / Ca2 +,A Gene product of Frizzled Related Protein or FRP of the Wnt / Ca2 + Pathway is indicative of a State glaucomatous.Claim 7: a method for the treatment of glaucoma in a patient, the method comprises administering to the patient a composition comprising a therapeutically effective amount of a compound that modulates the level of bioactivity or a component of the Wnt / Ca2 + Pathway, a pro Duct of the Frizzled Gene related to Wnt / Ca2 + Pathway or FRP of the Wnt / Ca2 + Pathway.Claim 8: The Method according to claim 7, wherein the compound is selected from the group consisting of a Protein, a Peptide, a peptidomimetic Small Molecule or a nucleic acid.
机译:权利要求1:一种诊断患者中的青光眼的方法,该方法包括以下步骤:(a)获得患者的样品;或(b)检测Wnt / Ca2 +通路(卷曲的相关蛋白基因Wnt / Ca2 +通路的产物)的生物活性成分的水平。FRP或通过Wnt / Ca2 +通路,和(c)比较正常样品中Wnt / Ca2 +途径的生物活性或组分水平,卷曲蛋白相关蛋白或Wnt / Ca2 +水平的FRP的基因产物,其中生物活性组分或异常水平Wnt的途径Ca 2+,Wnt // Ca 2+途径的卷曲相关蛋白或FRP的基因产物指示青光眼状态。权利要求7:用于治疗患者中的青光眼的方法,该方法包括向患者施用组合物包含治疗有效量的可调节生物活性水平的化合物或Wnt / Ca2 +途径的成分,与Wnt / Ca2 +途径相关的卷曲基因产品或Wnt / Ca2 +的FRP权利要求8:根据权利要求7的方法,其中所述化合物选自t该组由蛋白质,肽,拟肽小分子或核酸组成。

著录项

  • 公开/公告号AR039967A1

    专利类型

  • 公开/公告日2005-03-09

    原文格式PDF

  • 申请/专利权人 ALCON INC.;

    申请/专利号AR2003P101569

  • 发明设计人

    申请日2003-05-05

  • 分类号A61K45/06;A61K38/00;A61K31/7105;A61K31/711;A61P27/06;

  • 国家 AR

  • 入库时间 2022-08-21 22:18:51

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