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9 条记录 (耗时 0.054 秒)

    REINFORCED WASTE COLLECTION DEVICE
    6.
    发明公开
    REINFORCED WASTE COLLECTION DEVICE 审中-公开

    公开(公告)号：US20240116703A1

    公开(公告)日：2024-04-11

    申请号：US18263949

    申请日：2022-02-03

    申请人： Fabrice Andre

    发明人： Fabrice Andre

    IPC分类号： B65F1/16

    CPC分类号： B65F1/1623

    摘要： A waste collection device having a main body delimiting an internal collection volume, a movable door covering a side opening, a stiffening device for stiffening the main body that are configured to prevent the main body from twisting when the door is in the open position.

    Molecular in vitro diagnosis of breast cancer
    7.
    发明授权
    Molecular in vitro diagnosis of breast cancer 失效
    分子体外诊断乳腺癌

    公开(公告)号：US08299233B2

    公开(公告)日：2012-10-30

    申请号：US12811792

    申请日：2009-01-05

    申请人： Fabrice Andre ,  Stefan Michiels ,  Suzette Delaloge ,  Marc Spielmann ,  Philippe Dessen ,  Philippe Vielh

    发明人： Fabrice Andre ,  Stefan Michiels ,  Suzette Delaloge ,  Marc Spielmann ,  Philippe Dessen ,  Philippe Vielh

    IPC分类号： C07H21/04

    CPC分类号： C12Q1/6886 ,  C12Q2600/112 ,  C12Q2600/156

    摘要： The invention relates to the use of a multiplicity of polynucleotide probe sets, the multiplicity of polynucleotide probe sets consisting in a combination of pools of polynucleotide probe sets, each polynucleotide probe set containing at least one polynucleotide probe chosen among a library of nucleic acid sequences, the polynucleotide probes involved in the combination of pools of polynucleotide probe sets of the multiplicity of polynucleotide probe sets being such that each polynucleotide probe specifically hybridizes with one gene, and/or at least one of its variants when present, for determining the variation of expression at least 12 genes, and their variants when present, in order to diagnose the benign or malignant state of a breast tumor.

    摘要翻译： 本发明涉及多种多核苷酸探针组的使用，多核苷酸探针组由多核苷酸探针组的组合组成，每个多核苷酸探针组含有选自核酸序列文库中的至少一种多核苷酸探针， 涉及多个多核苷酸探针组的多核苷酸探针组的组合的多核苷酸探针使得每个多核苷酸探针与一个基因和/或其存在的至少一个变体特异性杂交用于确定表达的变化 至少12个基因及其变异体，以便诊断乳腺肿瘤的良性或恶性状态。

    MOLECULAR IN VITRO DIAGNOSIS OF BREAST CANCER
    9.
    发明申请
    MOLECULAR IN VITRO DIAGNOSIS OF BREAST CANCER 失效
    分子乳腺癌的分子诊断

    公开(公告)号：US20110009286A1

    公开(公告)日：2011-01-13

    申请号：US12811792

    申请日：2009-01-05

    申请人： Fabrice Andre ,  Stefan Michiels ,  Suzette Delaloge ,  Marc Spielmann ,  Philippe Dessen ,  Philippe Vielh

    发明人： Fabrice Andre ,  Stefan Michiels ,  Suzette Delaloge ,  Marc Spielmann ,  Philippe Dessen ,  Philippe Vielh

    IPC分类号： C40B30/04 ,  C40B40/06

    CPC分类号： C12Q1/6886 ,  C12Q2600/112 ,  C12Q2600/156

    摘要： The invention relates to the use of a multiplicity of polynucleotide probe sets, the multiplicity of polynucleotide probe sets consisting in a combination of pools of polynucleotide probe sets, each polynucleotide probe set containing at least one polynucleotide probe chosen among a library of nucleic acid sequences, the polynucleotide probes involved in the combination of pools of polynucleotide probe sets of the multiplicity of polynucleotide probe sets being such that each polynucleotide probe specifically hybridizes with one gene, and/or at least one of its variants when present, for determining the variation of expression at least 12 genes, and their variants when present, in order to diagnose the benign or malignant state of a breast tumor.

    摘要翻译： 本发明涉及多种多核苷酸探针组的使用，多核苷酸探针组由多核苷酸探针组的组合组成，每个多核苷酸探针组含有选自核酸序列文库中的至少一种多核苷酸探针， 涉及多个多核苷酸探针组的多核苷酸探针组的组合的多核苷酸探针使得每个多核苷酸探针与一个基因和/或其存在的至少一个变体特异性杂交用于确定表达的变化 至少12个基因及其变异体，以便诊断乳腺肿瘤的良性或恶性状态。