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    • 2. 发明申请
    • Hb-954 as a target for modulating angiogenesis
    • Hb-954作为调节血管发生的靶标
    • US20050202017A1
    • 2005-09-15
    • US10525456
    • 2003-08-29
    • Katharine DixonGene LiauCynthia Serdikoff
    • Katharine DixonGene LiauCynthia Serdikoff
    • A61K38/00A61K39/395A61K48/00C07K14/705C07K16/30C12N1/21C12N15/12G01N33/574
    • C07K14/705A61K38/00
    • The invention describes assays for the identification of compounds useful for the modulation of angiogenesis. The methods of the invention involve cell-free and cell-based assays that identify compounds which bind to and/or activate or inhibit the activity of HB-954, a G protein-coupled receptor, optionally followed by an in vivo assay of the effect of the compound on angiogenesis. The invention also describes compounds which bind to and/or activate or inhibit the activity of HB-954 as well as pharmaceutical compositions comprising such compounds. In addition, the invention includes nucleic acid molecules comprising a nucleotide sequence encoding all or a portion of HB-954, gene therapy vectors comprising such sequences, polypeptides comprising all or a portion of HB-954 and antibodies directed against HB-954.
    • 本发明描述了用于鉴定可用于调节血管发生的化合物的测定。 本发明的方法包括无细胞和基于细胞的测定法,其鉴定结合和/或活化或抑制G蛋白偶联受体的HB-954的活性的化合物,任选地随后进行体内测定 的化合物对血管生成的影响。 本发明还描述了结合和/或活化或抑制HB-954活性的化合物以及包含这些化合物的药物组合物。 此外,本发明包括包含编码HB-954的全部或一部分的核苷酸序列的核酸分子,包含此类序列的基因治疗载体,包含全部或部分HB-954的多肽和针对HB-954的抗体。
    • 3. 发明申请
    • Novel Hyaluronan-Binding Proteins and Encoding Genes
    • 新型透明质酸结合蛋白和编码基因
    • US20070213255A1
    • 2007-09-13
    • US11550102
    • 2006-10-17
    • Gregg HastingsGene LiauElena Tsifrina
    • Gregg HastingsGene LiauElena Tsifrina
    • A61K38/00C07H21/04C07K16/00C12N15/00C12N5/00C12P21/00C12Q1/68G01N33/53
    • G01N33/5008C07K14/705G01N33/502G01N33/68G01N2333/47
    • The present invention relates to full-length WF-HABP, WF-HABP, OE-HABP, and BM-HABP, novel members of the hyaluronan receptor family. The invention provides isolated nucleic acid molecules encoding human to full-length WF-HABP, WF-HABP, OE-HABP, and BM-HABP receptors. Full-length WF-HABP, WF-HABP, OE-HABP, and BM-HABP polypeptides are also provided, as are vectors, host cells and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of full-length WF-HABP, WF-HABP, OE-HABP, and BM-HABP receptor activity. Also provided are diagnostic methods for detecting disease states related to the aberrant expression of full-length WF-HABP, WF-HABP, OE-HABP, and BM-HABP receptors. Further provided are therapeutic methods for treating disease states including, but not limited to, proliferative conditions, metastasis, inflammation, ischemia, host defense dysfunction, immune surveillance dysfunction, arthritis, multiple sclerosis, autoimmunity, immune dysfunction, and allergy.
    • 本发明涉及全长WF-HABP,WF-HABP,OE-HABP和BM-HABP,是透明质酸受体家族的新成员。 本发明提供了编码人全长WF-HABP,WF-HABP,OE-HABP和BM-HABP受体的分离的核酸分子。 还提供了全长WF-HABP,WF-HABP,OE-HABP和BM-HABP多肽,载体,宿主细胞和用于制备它们的重组方法也是如此。 本发明还涉及用于鉴定全长WF-HABP,WF-HABP,OE-HABP和BM-HABP受体活性的激动剂和拮抗剂的筛选方法。 还提供了用于检测与全长WF-HABP,WF-HABP,OE-HABP和BM-HABP受体的异常表达相关的疾病状态的诊断方法。 进一步提供治疗疾病状态的治疗方法,包括但不限于增殖性病症,转移,炎症,缺血,宿主防御功能障碍,免疫监视功能障碍,关节炎,多发性硬化,自身免疫,免疫功能障碍和过敏。