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    • 21. 发明公开
    • 사구체 경화증 발생을 효과적으로 억제하는 IL-10 발현 재조합 바이러스 벡터 및 이를 이용한 신부전증의 유전자 요법
    • 表达人IL-10的重组病毒载体用于抑制GLOMERULOSCLEROSIS和基因治疗使用同样方法治疗肾衰竭
    • KR1020020076001A
    • 2002-10-09
    • KR1020010015892
    • 2001-03-27
    • 주식회사 웰진
    • 박종구최영국
    • C12N15/86
    • A61K38/2066C07K14/5428C12N15/861
    • PURPOSE: Provided are a recombinant virus vector for the expression of cytokine IL-10 which has a strong anti-inflammation effect and is thus effective for the inhibition of glomerulosclerosis, and a gene therapy using the same for curing renal failure. CONSTITUTION: The recombinant virus vector, AdCMVhIL-10IL-10(KCTC 0958BP), expresses IL-10 to effectively inhibit glomerulosclerosis. It is selected from the group consisting of retrovirus, adenovirus, AAV(adeno-associated virus), herpes simplex derived vector; naked DNA; and a complex of liposome, polycationic lipid, polyethyleneimine, poluL-lysine, polyD-lysine and inactive virus vector(adenovirus, sendai virus, AAV). cDNA of human IL-10 gene is represented by the SEQ ID NO:1. A pharmaceutical composition for the prevention, diagnosis, and treatment of renal failure contains recombinant virus vector for the expression of IL-10 and IL-10 protein as active ingredients.
    • 目的:提供用于表达细胞因子IL-10的重组病毒载体,其具有强烈的抗炎作用,因此对抑制肾小球硬化有效,并且使用其用于治疗肾衰竭的基因治疗。 构成:重组病毒载体AdCMVhIL-10IL-10(KCTC 0958BP)表达IL-10以有效抑制肾小球硬化。 选自逆转录病毒,腺病毒,AAV(腺相关病毒),单纯疱疹病毒载体; 裸DNA; 和脂质体,聚阳离子脂质,聚乙烯亚胺,poluL-赖氨酸,聚-D-赖氨酸和非活性病毒载体(腺病毒,发病病毒,AAV)的复合物。 人IL-10基因的cDNA由SEQ ID NO:1表示。 用于预防,诊断和治疗肾衰竭的药物组合物含有用于表达IL-10和IL-10蛋白作为活性成分的重组病毒载体。
    • 22. 发明公开
    • 종양 특이증식 재조합 아데노바이러스 및 그를 이용하여 종양세포만을 특이적으로 형질전환시키는 방법
    • 肿瘤特异性重组腺病毒和使用其消除肿瘤细胞的方法
    • KR1020010017484A
    • 2001-03-05
    • KR1019990033011
    • 1999-08-12
    • 학교법인연세대학교
    • 이희란김주항김재성
    • C12N15/86
    • C12N15/861A61K35/761
    • PURPOSE: Provided is tumor-specific recombinant Adenovirus which does not proliferate in normal cells, but shows remarkable self-proliferation activity in tumor cells where the function of protein p53 is inactivated. CONSTITUTION: Adenovirus is manipulated to remove a gene coding a protein of 55 kDa, which binds to p53 protein, from E1B gene thereof, so that a recombinant Adenovirus proliferates specifically in a tumor cell. A method for removing tumor cells using the Adenovirus comprises the following steps of: i) removing a gene fragment which is located on gene E1B of Adenovirus type Ad 5, and codes 55kDa protein binding to p53 protein, to prepare recombinant Adenovirus YKL-1(KFCC-11099), multiplying the virus in host cells, and separating purely the virus; ii) infecting tumor cells with the recombinant Adenovirus in 0.1-10 of MOI(multiplicity of infection); iii) cultivating at 37 deg.C for 8-10 days and removing infected tumor cells.
    • 目的:提供在正常细胞中不增殖的肿瘤特异性重组腺病毒,但在蛋白p53的功能失活的肿瘤细胞中显示出显着的自身增殖活性。 构成:操纵腺病毒以从E1B基因中除去编码结合p53蛋白的55kDa的蛋白质的基因,使得重组腺病毒在肿瘤细胞中特异性增殖。 使用腺病毒除去肿瘤细胞的方法包括以下步骤:i)除去位于腺病毒Ad5基因的E1B上的基因片段,编码结合p53蛋白的55kDa蛋白质,制备重组腺病毒YKL-1( KFCC-11099),将宿主细胞中的病毒繁殖,纯化分离病毒; ii)用0.1-10的MOI感染肿瘤细胞(重复感染); iii)在37℃下培养8-10天,并去除感染的肿瘤细胞。
    • 26. 发明公开
    • 하이브리드 바이러스 유전자 전달체 및 그의 용도
    • 混合病毒基因传递系统及其用途
    • KR1020160029198A
    • 2016-03-15
    • KR1020140117721
    • 2014-09-04
    • 부산대학교 산학협력단
    • 유소영
    • C12N15/85C12N15/861A61K48/00
    • C12N15/85A61K48/00C12N15/00C12N15/861
    • 본발명은박테리오파지및 아데노부속바이러스하이브리드유전자전달체및 이를코딩하는폴리뉴클레오티드에관한것이다. 또한, 본발명은상기하이브리드유전자전달체를제조하는방법에관한것이다. 또한, 본발명은상기하이브리드유전자전달체를포함하는약학적조성물및 진단용조성물에관한것이다. 본발명에따른하이브리드바이러스유전자전달체는파지의껍질에표적할수 있는기능성펩타이드를발현하도록하고, 표적세포에전달은바이러스-숙주간전달이아닌발현된기능성펩타이드에의한전달이되도록하여예기치않은면역반응을막을수 있으며, 바이러스내에아데노부속바이러스의유전자정보를실어서숙주내에들어간후 유전자정보가무작위로들어가지않고효율적으로발현되도록할 수있는바, 효과적이고효율적인유전자전달체로활용될수 있다.
    • 本发明涉及噬菌体和腺相关病毒的杂交基因递送及其编码的多核苷酸。 本发明还涉及一种用于产生杂交基因递送的方法。 此外,本发明涉及含有杂交基因递送的诊断组合物和药物组合物。 根据本发明,杂交病毒基因递送可以诱导能够靶向噬菌体衣壳的功能肽的表达。 此外,杂交病毒基因递送进行由表达的功能性肽介导的靶细胞递送,而不是病毒与宿主之间的递送,从而可以避免意想不到的免疫应答。 此外,通过将腺相关病毒的遗传信息添加到病毒中,可以有效地表达遗传信息而不是随机插入病毒转染到宿主中。 因此,杂交病毒基因递送可以用作有效和有效的基因递送。