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    • 3. 发明公开
    • Dkk1 또는 sFRP4 억제제를 함유한 비만 예방용 조성물
    • 用于防止含有DKK1或SFRP4的抑制剂的成分的组合物
    • KR1020100051195A
    • 2010-05-17
    • KR1020080110230
    • 2008-11-07
    • 서울대학교산학협력단
    • 강경선박정란
    • A61K39/395A61P3/04
    • A61K35/28A61K39/39533Y10S514/909
    • PURPOSE: An obesity preventive composition containing a Dkk1(dickkopf-related protein 1) OR a sFRP4(secreted frizzled-related protein 4) inhibitor is provided to control the differentiation of MSC to a fat cell. CONSTITUTION: An obesity preventive composition contains a Dkk1 OR a sFRP4 inhibitor. The Dkk1 inhibitor is an antibody for the Dkk1 which expresses a siRNA(small interfering RNA) targeting the Dkk1. The sFRP4 inhibitor is the antibody for the sFRP4 which expresses the siRNA targeting the sFRP4. The differentiation of MSC(mesenchymal stem cells) is inhibited by the Dkk1 or the sFRP4 inhibitor by processing the MSC with the inhibitors for controlling the differentiation into a fat cell.
    • 目的:提供含有Dkk1(dickkopf相关蛋白1)或sFRP4(分泌性卷曲相关蛋白4)抑制剂的肥胖预防组合物,以控制MSC与脂肪细胞的分化。 构成:肥胖预防组合物含有Dkk1 OR或sFRP4抑制剂。 Dkk1抑制剂是Dkk1的抗体,其表达靶向Dkk1的siRNA(小干扰RNA)。 sFRP4抑制剂是表达靶向sFRP4的siRNA的sFRP4的抗体。 MSC(间充质干细胞)的分化被Dkk1或sFRP4抑制剂抑制,通过用控制分化成脂肪细胞的抑制剂处理MSC。
    • 10. 发明公开
    • 피부세포로부터 기능성 인슐린 생산 세포의 직접 제조방법
    • 功能性胰岛素从人类纤维蛋白生成细胞的直接制备
    • KR1020130116155A
    • 2013-10-23
    • KR1020120118708
    • 2012-10-24
    • 주식회사 강스템바이오텍서울대학교산학협력단
    • 강경선서광원김미현
    • C12N5/071C12N15/85C12N5/10A61K35/12
    • PURPOSE: A method for directly producing functional insulin-producing cells from skin cells is provided to directly convert human somatic cells into insulin-producing cells without dedifferentiation into pluripotent cells and to obtain the insulin-producing cells which normally secrete insulin by glucose stimulation. CONSTITUTION: A method for producing insulin-producing cells comprises the step of promoting transcription of PDX-1 gene in somatic cells which do not produce insulin. The method directly converts the somatic cells into insulin-producing cells without dedifferentiation into cells with stemness. The step for promoting transcription of PDX-1 gene comprises the steps of transfecting cells by SMAD2 and transducing anti-Let7i by culturing the transfected cells for 2-10 days. [Reference numerals] (AA) Smad2 trait infection; (BB) Second day; (CC) FGM medium + 1% BSA; (DD) Anti-Let7i trait infection; (EE) EGM medium + 1% BSA; (FF) Seventh day; (GG) Glucose simulation index
    • 目的:提供从皮肤细胞直接产生功能性胰岛素生成细胞的方法,以将人体细胞直接转化成胰岛素产生细胞,而不去分化成多能细胞,并获得通过葡萄糖刺激通常分泌胰岛素的胰岛素产生细胞。 构成:产生胰岛素的细胞的方法包括促进PDX-1基因在不产生胰岛素的体细胞中的转录的步骤。 该方法直接将体细胞转化为产生胰岛素的细胞,而无需去分化成具有干细胞的细胞。 促进PDX-1基因转录的步骤包括通过SMAD2转染细胞并通过培养转染细胞2-10天来转导抗Let7i的步骤。 (附图标记)(AA)Smad2性状感染; (BB)第二天; (CC)FGM培养基+ 1%BSA; (DD)抗let7i性状感染; (EE)EGM培养基+ 1%BSA; (FF)第七天; (GG)葡萄糖模拟指数