PROCESS AND METHOD FOR DIAGNOSING ALZHEIMER'S DISEASE
    2.
    发明申请
    PROCESS AND METHOD FOR DIAGNOSING ALZHEIMER'S DISEASE 失效
    用于诊断阿尔茨海默病的方法和方法

    公开(公告)号:US20110086776A1

    公开(公告)日:2011-04-14

    申请号:US12935098

    申请日:2009-03-30

    IPC分类号: C40B30/04 C40B40/06

    摘要: The present invention concerns methods and compositions usable for diagnosing Alzheimer's disease in mammals, in particular humans. It particularly describes serum markers for Alzheimer's disease and their use in diagnostic methods. It also concerns tools and/or kits usable for implementing these methods (reagents, probes, primers, antibodies, chips, cells, etc.), their preparation and their use. The invention is usable to detect the presence or progression of Alzheimer's disease in mammals, including in the early phase, as well as for predicting the efficacy of an Alzheimer's disease treatment.

    摘要翻译: 本发明涉及可用于诊断哺乳动物,特别是人类中的阿尔茨海默氏病的方法和组合物。 它特别描述了阿尔茨海默病的血清标志物及其在诊断方法中的应用。 它还涉及可用于实施这些方法(试剂,探针,引物,抗体,芯片,细胞等)的工具和/或试剂盒,其制备及其用途。 本发明可用于检测哺乳动物中的阿尔茨海默病的存在或进展,包括在早期阶段以及预测阿尔茨海默病治疗的功效。

    Procedure and methods for detecting alzheimers's disease
    3.
    发明申请
    Procedure and methods for detecting alzheimers's disease 审中-公开
    检测阿尔茨海默病的程序和方法

    公开(公告)号:US20100055682A1

    公开(公告)日:2010-03-04

    申请号:US12227374

    申请日:2007-05-14

    摘要: This application concerns methods and compositions that can be used for detecting the Alzheimer disease in mammals, particularly in humans. It describes in particular serum markers for Alzheimer's disease and the way they are used for diagnostic procedures. It also concerns tools and/or kits that can be used for applying these procedures (reagents, probes, primers, antibodies, chips, cells, etc.) with the preparation thereof and the way to use them. The invention can be used to detect the presence or the progression of Alzheimer illness in mammals, including at early stages of the disease.

    摘要翻译: 本申请涉及可用于检测哺乳动物,特别是人类中的阿尔茨海默病的方法和组合物。 它特别描述了阿尔茨海默病的血清标志物及其用于诊断程序的方法。 它还涉及可用于应用这些程序(试剂,探针,引物,抗体,芯片,细胞等)及其使用方法的工具和/或试剂盒。 本发明可用于检测哺乳动物中阿尔茨海默病的存在或进展,包括在疾病的早期阶段。

    Process and method for diagnosing Alzheimer's disease
    4.
    发明授权
    Process and method for diagnosing Alzheimer's disease 失效
    诊断阿尔茨海默病的过程和方法

    公开(公告)号:US08481701B2

    公开(公告)日:2013-07-09

    申请号:US12935098

    申请日:2009-03-30

    IPC分类号: C07H21/02 C07H21/04 C12Q1/68

    摘要: The present invention concerns methods and compositions usable for diagnosing Alzheimer's disease in mammals, in particular humans. It particularly describes serum markers for Alzheimer's disease and their use in diagnostic methods. It also concerns tools and/or kits usable for implementing these methods (reagents, probes, primers, antibodies, chips, cells, etc.), their preparation and their use. The invention is usable to detect the presence or progression of Alzheimer's disease in mammals, including in the early phase, as well as for predicting the efficacy of an Alzheimer's disease treatment.

    摘要翻译: 本发明涉及可用于诊断哺乳动物,特别是人类中的阿尔茨海默氏病的方法和组合物。 它特别描述了阿尔茨海默病的血清标志物及其在诊断方法中的应用。 它还涉及可用于实施这些方法(试剂,探针,引物,抗体,芯片,细胞等)的工具和/或试剂盒,其制备及其用途。 本发明可用于检测哺乳动物中的阿尔茨海默病的存在或进展,包括在早期阶段以及预测阿尔茨海默病治疗的功效。

    P53 protein variants and therapeutic uses thereof
    5.
    发明授权
    P53 protein variants and therapeutic uses thereof 失效
    P53蛋白变体及其治疗用途

    公开(公告)号:US06326464B1

    公开(公告)日:2001-12-04

    申请号:US08983035

    申请日:1998-02-20

    IPC分类号: A61K3800

    摘要: Proteins derived from the product of tumor suppressor gene p53 and having enhanced functions for therapeutical use are disclosed. The proteins advantageously have enhanced tumour suppressor and programmed cell death inducer functions, particularly in proliferative disease contexts where wild-type p53 protein is inactivated. Nucleic acids coding for such molecules, vectors containing same, and therapeutical use thereof, particularly in gene therapy, are also disclosed.

    摘要翻译: 公开了衍生自肿瘤抑制基因p53的产物并具有增强的治疗用功能的蛋白质。 蛋白质有利地具有增强的肿瘤抑制因子和程序性细胞死亡诱导物功能,特别是在野生型p53蛋白被灭活的增殖性疾病背景中。 还公开了编码这种分子的核酸,含有它们的载体及其治疗用途,特别是在基因治疗中。

    DETECTION AND TREATMENT OF CANCERS
    7.
    发明申请
    DETECTION AND TREATMENT OF CANCERS 审中-公开
    检测和治疗癌症

    公开(公告)号:US20090298766A1

    公开(公告)日:2009-12-03

    申请号:US12293124

    申请日:2007-03-15

    摘要: The present invention relates to methods and compositions for the detection and treatment of melanoma and skin cancers. More particularly, the invention discloses that BCSC-1 expression is altered in melanoma and skin cancer cells, allowing the design of effective detection methods and kits for such conditions. The invention also shows that restoring or increasing expression of BCSC-1 in melanoma and skin cancer cells suppresses tumorigenicity and represents a novel and effective approach for the treatment of melanoma and skin cancers. The invention may be used to detect the presence, stage or type of melanoma and skin cancers, as well as any predisposition thereto. The invention may be used in any mammalian subject, particularly human subjects.

    摘要翻译: 本发明涉及用于检测和治疗黑素瘤和皮肤癌的方法和组合物。 更具体地,本发明公开了BCSC-1表达在黑素瘤和皮肤癌细胞中改变,允许为这种条件设计有效的检测方法和试剂盒。 本发明还显示,恢复或增加黑素瘤和皮肤癌细胞中BCSC-1的表达抑制致瘤性,并且代表治疗黑素瘤和皮肤癌的新颖有效的方法。 本发明可用于检测黑素瘤和皮肤癌的存在,阶段或类型,以及其任何倾向。 本发明可用于任何哺乳动物受试者,特别是人类受试者。

    METHODS UTILIZING DIFFERENTIAL SPLICING EVENTS IN BLOOD CELLS FOR THE DETECTION OF PATHOLOGICAL EVENTS
    8.
    发明申请
    METHODS UTILIZING DIFFERENTIAL SPLICING EVENTS IN BLOOD CELLS FOR THE DETECTION OF PATHOLOGICAL EVENTS 审中-公开
    方法利用血液细胞中的差异性分离事件检测病理活动

    公开(公告)号:US20090264301A1

    公开(公告)日:2009-10-22

    申请号:US12494039

    申请日:2009-06-29

    IPC分类号: C40B30/00

    CPC分类号: G01N33/56972 C12Q1/6809

    摘要: The present invention concerns new compositions and methods for the detection of pathological events. It more specifically concerns methods for the detection in vitro of the presence of a pathology or a pathological event in a subject, comprising taking a sample of blood cells from the subject and determining, in this sample, the presence of blood cells presenting a physiological state characteristic of the pathology. The invention also concerns the tools, kits and compositions for the implementation of such methods, as well as their uses in the field of human and animal health, or in experimental research for example.

    摘要翻译: 本发明涉及用于检测病理事件的新组合物和方法。 更具体地涉及在体外检测受试者中病理学或病理学事件的存在的方法,其包括从受试者中取出血细胞样品,并在该样品中确定呈现生理状态的血细胞的存在 病理特征。 本发明还涉及用于实施这些方法的工具,试剂盒和组合物,以及它们在人类和动物健康领域或在实验研究领域中的用途。

    Genetic markers of toxicity preparation and uses
    9.
    发明授权
    Genetic markers of toxicity preparation and uses 失效
    毒性制剂和用途的遗传标记

    公开(公告)号:US06509153B1

    公开(公告)日:2003-01-21

    申请号:US09456370

    申请日:1999-12-08

    IPC分类号: C12Q168

    摘要: The present invention describes new methods for the determination of the potential toxicity of test compounds, as well as the kits and tools for the implementation of these methods. The invention also describes methods for generating nucleic acid sequences that can be used as genetic markers of toxicity. The invention is based in particular on the creation of differential nucleic acid banks characteristic of situations in which cell viability and/or proliferation are deregulated, and on the demonstration that these banks can be used to evaluate the toxicity profile of compounds with reliability and high sensitivity. The invention is of special utility in the pharmaceutical industry for analysis of the toxicity profile of compounds involved in drug development and/or in pharmaceutical compositions.

    摘要翻译: 本发明描述了用于确定测试化合物的潜在毒性的新方法,以及用于实施这些方法的试剂盒和工具。 本发明还描述了用于产生可用作毒性遗传标记物的核酸序列的方法。 本发明特别地基于创造细胞活力和/或增殖失调的情况特征的差异核酸库,并且证明这些银行可以用于评估具有可靠性和高灵敏度的化合物的毒性特征 。 本发明在制药工业中用于分析涉及药物开发和/或药物组合物的化合物的毒性特征。

    Qualitative differential screening
    10.
    发明授权
    Qualitative differential screening 有权
    定性差异筛选

    公开(公告)号:US08003375B2

    公开(公告)日:2011-08-23

    申请号:US12622364

    申请日:2009-11-19

    IPC分类号: C07H21/04 C12Q1/68 C12M1/34

    摘要: The invention concerns a method for identifying and/or cloning nucleic acid regions representing qualitative differences associated with alternative splicing events and/or with insertions, deletions located in RNA transcribed genome regions, between two physiological situations, comprising either hybridization of RNA derived from the test situation with cDNA's derived from the reference situation and/or reciprocally, or double-strand hybridization of cDNA derived from the test situation with cDNA's derived from the reference situation; and identifying and/or cloning nucleic acids representing qualitative differences. The invention also concerns compositions or banks of nucleic acids representing qualitative differences between two physiological situations, obtainable by the above method, and their use as probe, for identifying genes or molecules of interest, or still for example in methods of pharmacogenomics, and profiling of molecules relative to their therapeutic and/or toxic effects. The invention further concerns the use of dysregulation of splicing RNA as markers for predicting molecule toxicity and/or efficacy, and as markers in pharmacogenomics.

    摘要翻译: 本发明涉及用于鉴定和/或克隆代表与选择性剪接事件相关的定性差异的核酸区域的方法和/或在两个生理情境之间的位于RNA转录基因组区域中的插入,缺失的方法,其包括衍生自测试的RNA的杂交 来自参考情况的cDNA的情况和/或来自测试情况的​​cDNA的双链杂交和/或来自参考情况的cDNA的双链杂交; 以及鉴定和/或克隆代表定性差异的核酸。 本发明还涉及表示通过上述方法获得的两种生理情况之间的定性差异的核酸组合物或组,以及它们作为探针的用途,用于鉴定感兴趣的基因或分子,或者仍然例如在药物基因组学的方法中,以及 分子相对于其治疗和/或毒性作用。 本发明还涉及使用拼接RNA的调节作为用于预测分子毒性和/或功效的标记物,以及作为药物基因组学中的标记物。