Preparation of immortalized cells
    9.
    发明授权
    Preparation of immortalized cells 失效
    永生化细胞的制备

    公开(公告)号:US5830682A

    公开(公告)日:1998-11-03

    申请号:US770895

    申请日:1996-12-13

    申请人: Emma E. Moore

    发明人: Emma E. Moore

    摘要: All lines have been prepared from growth suppressor gene deficient animals. The cells include immortalized precursor cells and differentiated cells such as osteoclast precursors, osteoblast precursors, megakaryocytes, osteoclasts, osteoblasts, pancreatic .alpha.-cells, pancreatic .beta.-cells, pancreatic .delta.-cells, adipocytes, macrophages, chondrocytes, dendritic cells, hepatocytes, myocytes and prostatic cells. The cells are useful for constructing cDNA and protein libraries, screening agonists and antagonists of compounds and factors that affect metabolic pathways of specific cells and generating cell-specific antibodies.

    摘要翻译: 所有的系都是由生长抑制基因缺陷动物制备的。 细胞包括永生化前体细胞和分化细胞如破骨细胞前体,成骨细胞前体,巨核细胞,破骨细胞,成骨细胞,胰腺α细胞,胰腺β-细胞,胰腺β-细胞,脂肪细胞,巨噬细胞,软骨细胞,树突状细胞,肝细胞,肌细胞 和前列腺细胞。 细胞可用于构建cDNA和蛋白质文库,筛选化合物的激动剂和拮抗剂以及影响特定细胞的代谢途径并产生细胞特异性抗体的因子。

    Pharmaceutical composition comprising FGF18 and IL-1 antagonist and method of use
    10.
    发明授权
    Pharmaceutical composition comprising FGF18 and IL-1 antagonist and method of use 有权
    包含FGF18和IL-1拮抗剂的药物组合物及其使用方法

    公开(公告)号:US07749965B2

    公开(公告)日:2010-07-06

    申请号:US12103420

    申请日:2008-04-15

    IPC分类号: A61K38/20 A61K38/18 A61F2/00

    摘要: FGF18 is known to stimulate the proliferation of chondrocytes, bone, and nervous tissue, resulting in repair of diseased tissue. When an IL-1 antagonist is administered in addition to FGF18, the effects on the IL-1 mediated disease and also, the effect on cartilage, bone, and nervous cell proliferation, are found to be greater than administration of FGF18 or the IL-1 antagonist alone. The present invention encompasses a pharmaceutical composition that combines FGF18 with IL-1 antagonist and methods of treating IL-1 mediated disease using this pharmaceutical composition.

    摘要翻译: 已知FGF18可刺激软骨细胞,骨骼和神经组织的增殖,导致病变组织的修复。 当除FGF18外施用IL-1拮抗剂时,发现对IL-1介导的疾病的影响以及对软骨,骨骼和神经细胞增殖的影响大于施用FGF18或IL- 1拮抗剂。 本发明包括使用该药物组合物将FGF18与IL-1拮抗剂组合的药物组合物和治疗IL-1介导的疾病的方法。