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    • 6. 发明申请
    • PREDICTION OF CANCER BY DETECTION OF ATM MUTATIONS
    • 通过检测ATM突变预测癌症
    • WO03025203A3
    • 2003-05-22
    • PCT/US0230015
    • 2002-09-20
    • QUARK BIOTECH INCGILAD SHLOMITYAHALOM JOACHIM
    • GILAD SHLOMITYAHALOM JOACHIM
    • C12Q1/68C07H21/04
    • C12Q1/6827C12Q1/6886C12Q2600/156
    • There is provided a method of testing a subject to determine if the subject has a predisposition for developing a cancer, a cancer of epithelial origin such as lung cancer, colon cancer, prostate cancer, ovarian cancer, bladder cancer, and cancer of the pancreas, and also a lymphoproliferative malignancy such as Hodgkin's disease and non-Hodgkin's lymphoma. This method includes the steps of detecting a mutation in the open reading frame of the ATM gene SEQ.ID.NO:1 in a cDNA sample or a genomic DNA sample from the subject, which mutation is selected from the group consisting of the mutations set forth in Table 3 and Table 4 or, detecting a mutation in the mRNA corresponding to the open reading frame of the ATM gene SEQ.ID.NO:1 in a mRNA sample from the subject, which mutation is selected from the group consisting of RNA complementary to the mutations set forth in Table 3 and Table 4, wherein the presence of such a mutation indicates that the subject has a predisposition for developing cancer. Also provided is an isolated cDNA molecules, oligonucleotide probes, and kits for detection and prediction of cancer.
    • 提供了一种测试受试者以确定受试者是否具有发展癌症,上皮来源癌症如肺癌,结肠癌,前列腺癌,卵巢癌,膀胱癌和胰腺癌的倾向的方法, 以及淋巴增生性恶性肿瘤如霍奇金病和非霍奇金淋巴瘤。 该方法包括检测cDNA样品中的ATM基因SEQ.ID.NO:1的开放阅读框中的突变或来自受试者的基因组DNA样品中的突变,该突变选自突变组 在表3和表4中,或者检测来自受试者的mRNA样品中与ATM基因SEQ ID NO:1的开放阅读框相对应的mRNA的突变,该突变选自RNA 与表3和表4所示的突变互补,其中这种突变的存在表明受试者具有发生癌症的倾向。 还提供了分离的cDNA分子,寡核苷酸探针和用于癌症的检测和预测的试剂盒。