KITS FOR QUANTITATIVE DETECTION OF K-RAS MUTATIONS
    1.
    发明申请
    KITS FOR QUANTITATIVE DETECTION OF K-RAS MUTATIONS 审中-公开
    用于定量检测K-RAS突变的试剂盒

    公开(公告)号:US20120288862A1

    公开(公告)日:2012-11-15

    申请号:US13520176

    申请日:2010-12-29

    Applicant: Junpu Xu Zhao Chen

    Inventor: Junpu Xu Zhao Chen

    CPC classification number: C12Q1/6886 C12Q2600/106 C12Q2600/156

    Abstract: The present invention relates to an assay kit for quantitatively detecting k-ras gene mutations. Particularly, the present invention relates to detection method and a detection kit for K-ras gene mutations, which relates to the therapeutic efficacy of targeted molecular anti-cancer drugs. More particularly, the present invention relates to a fluorescent quantitative PCR method and kit for detecting mutations at hotspots of K-ras gene, together with the use thereof. The present invention detects the mutations at specific sites of K-ras gene, and can predict the therapeutic efficacy of anti-EGFR tyrosine kinase inhibitors. Therefore, it can provide a guidance to individualized treatments for cancer patients.

    Abstract translation: 本发明涉及用于定量检测k-ras基因突变的测定试剂盒。 特别地,本发明涉及K-ras基因突变的检测方法和检测试剂盒,涉及靶向分子抗癌药物的治疗功效。 更具体地,本发明涉及用于检测K-ras基因的热点的突变的荧光定量PCR方法和试剂盒及其用途。 本发明检测K-ras基因特异位点的突变,可预测抗EGFR酪氨酸激酶抑制剂的治疗效果。 因此,可为癌症患者的个体化治疗提供指导。

    METHODS OF MODULATING BINDING OF SON OF SEVENLESS TO PHOSPHATIDIC ACID AND IDENTIFYING COMPOUNDS THAT MODULATE SUCH BINDING
    4.
    发明申请
    METHODS OF MODULATING BINDING OF SON OF SEVENLESS TO PHOSPHATIDIC ACID AND IDENTIFYING COMPOUNDS THAT MODULATE SUCH BINDING 审中-公开
    调节方法将无盐酸溶解于磷酸和鉴定化合物的方法进行调节这种结合

    公开(公告)号:US20120301895A1

    公开(公告)日:2012-11-29

    申请号:US13568878

    申请日:2012-08-07

    CPC classification number: G01N33/5011 G01N2333/4706 G01N2333/916

    Abstract: The present invention relates to methods of modulating binding of Son of sevenless to phosphatidic acid and identifying compounds that modulate such binding. In particular, the present invention relates to a method of controlling pleckstrin homology domain-dependent membrane recruitment of Son of sevenless or histone folds domain-dependent membrane recruitment of Son of sevenless. Also disclosed are methods of controlling Ras and treating a subject for a condition mediated by Ras. The present invention also relates to a method of identifying compounds potentially effective in treating a condition mediated by Ras.

    Abstract translation: 本发明涉及调节7位儿子与磷脂酸结合的方法,并鉴定调节这种结合的化合物。 特别地,本发明涉及一种控制七分之一或七分之一子宫不育或组蛋白折叠域依赖性膜募集的睡眠蛋白同源结构域依赖性膜募集的方法。 还公开了控制Ras并治疗受试者由Ras介导的病症的方法。 本发明还涉及鉴定潜在有效治疗由Ras介导的病症的化合物的方法。

    REAGENT KIT FOR QUANTITATIVELY DETECTING THE MUTATIONS OF EPIDERMAL GROWTH FACTOR RECEPTOR(EGFR)
    5.
    发明申请
    REAGENT KIT FOR QUANTITATIVELY DETECTING THE MUTATIONS OF EPIDERMAL GROWTH FACTOR RECEPTOR(EGFR) 审中-公开
    定量检测天然生长因子受体(EGFR)突变的试剂盒

    公开(公告)号:US20120237935A1

    公开(公告)日:2012-09-20

    申请号:US13497527

    申请日:2010-09-20

    CPC classification number: C12Q1/6886 C12Q1/6851 C12Q2600/156

    Abstract: The present invention relates to a detection method and a detection kit for EGFR gene mutations, which relates to the therapeutic efficacy of molecular-targeted anti-cancer drugs. Particularly, the present invention relates to a fluorescent quantitative PCR method and kit for detecting mutations at hotspots of EGFR gene, together with the use thereof. The present invention detects the mutations at specific sites of EGFR gene, and can predict the therapeutic efficacy of EGFR tyrosine kinase inhibitors. Therefore, it can provide a guidance to individualize treatments for cancer patients.

    Abstract translation: 本发明涉及EGFR基因突变的检测方法和检测试剂盒,其涉及分子靶向抗癌药物的治疗功效。 特别地,本发明涉及用于检测EGFR基因热点突变的荧光定量PCR方法及试剂盒及其应用。 本发明检测EGFR基因特异位点的突变,可预测EGFR酪氨酸激酶抑制剂的治疗效果。 因此,可以为个体化癌症患者的治疗提供指导。

    METHODS OF MODULATING BINDING OF SON OF SEVENLESS TO PHOSPHATIDIC ACID AND IDENTIFYING COMPOUNDS THAT MODULATE SUCH BINDING
    6.
    发明申请
    METHODS OF MODULATING BINDING OF SON OF SEVENLESS TO PHOSPHATIDIC ACID AND IDENTIFYING COMPOUNDS THAT MODULATE SUCH BINDING 审中-公开
    调节方法将无盐酸溶解于磷酸和鉴定化合物的方法进行调节这种结合

    公开(公告)号:US20090137654A1

    公开(公告)日:2009-05-28

    申请号:US12114914

    申请日:2008-05-05

    CPC classification number: G01N33/5011 G01N2333/4706 G01N2333/916

    Abstract: The present invention relates to methods of modulating binding of Son of sevenless to phosphatidic acid and identifying compounds that modulate such binding. In particular, the present invention relates to a method of controlling pleckstrin homology domain-dependent membrane recruitment of Son of sevenless or histone folds domain-dependent membrane recruitment of Son of sevenless. Also disclosed are methods of controlling Ras and treating a subject for a condition mediated by Ras. The present invention also relates to a method of identifying compounds potentially effective in treating a condition mediated by Ras.

    Abstract translation: 本发明涉及调节7位儿子与磷脂酸结合的方法,并鉴定调节这种结合的化合物。 特别地,本发明涉及一种控制七分之一或七分之一子宫不育或组蛋白折叠域依赖性膜募集的睡眠蛋白同源结构域依赖性膜募集的方法。 还公开了控制Ras并治疗受试者由Ras介导的病症的方法。 本发明还涉及鉴定潜在有效治疗由Ras介导的病症的化合物的方法。

    KIT FOR QUANTITATIVE DETECTION OF BRAF MUTATION
    9.
    发明申请
    KIT FOR QUANTITATIVE DETECTION OF BRAF MUTATION 审中-公开
    用于定量检测BRAF MUTATION的工具包

    公开(公告)号:US20130095491A1

    公开(公告)日:2013-04-18

    申请号:US13581008

    申请日:2011-02-22

    CPC classification number: C12Q1/6886 C12Q1/686 C12Q2600/106 G01N2021/6432

    Abstract: The present invention relates to a method and assay kit for BRAF gene mutations which relates to the effect of molecule-targeting anti-tumor drug. Particularly, the present invention relates to a fluorescent quantitative PCR method and kit for detecting mutations at hotspots of BRAF gene, together with the use thereof. The present invention detects the mutations at specific sites of BRAF gene, and can predict the therapeutic efficacy of anti-EGFR tyrosine kinase inhibitors, an anti-tumor drug. Therefore, the present invention can provide a guidance to individualized treatments for cancer patients.

    Abstract translation: 本发明涉及涉及分子靶向抗肿瘤药物的作用的BRAF基因突变的方法和测定试剂盒。 特别地,本发明涉及用于检测BRAF基因热点突变的荧光定量PCR方法及试剂盒及其用途。 本发明检测BRAF基因特异位点的突变,可以预测抗EGFR酪氨酸激酶抑制剂抗肿瘤药物的疗效。 因此,本发明可以为癌症患者的个体化治疗提供指导。

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