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    • 21. 发明申请
    • METHOD OF ASSESSING COLORECTAL CANCER FROM A STOOL SAMPLE BY USE OF THE MARKER COMBINATION CALPROTECTIN AND HEMOGLOBIN/HAPTOGLOBIN COMPLEX
    • 通过使用标记卡培他滨和HEMOGLOBIN / HAPTOGLOBIN复合物从STOOL样品评估颜色性癌症的方法
    • WO2009065551A1
    • 2009-05-28
    • PCT/EP2008/009733
    • 2008-11-18
    • ROCHE DIAGNOSTICS GMBHF. HOFFMANN-LA-ROCHE AGKARL, JohannGARCZAREK, UrsulaWILD, Norbert
    • KARL, JohannGARCZAREK, UrsulaWILD, Norbert
    • G01N33/574
    • G01N33/57419G01N33/721G01N2333/4727G01N2333/805
    • The present invention relates to a method aiding in the assessment of colorectal cancer. The method especially is used in assessing the absence or presence of colorectal cancer in vitro. The method is for example practiced by analyzing biochemical markers, comprising measuring in a stool sample the concentration of the hemoglobin/haptoglobin complex and calprotectin and correlating the concentrations determined to the absence or presence of colorectal cancer. To further improve the assessment of colorectal cancer based on a method of this invention the level of one or more additional marker may be determined together with the hemoglobin/haptoglobin complex and calprotectin in a stool sample and be correlated to the absence or presence of colorectal cancer. The invention also relates to the use of a marker panel comprising the hemoglobin/haptoglobin complex and calprotectin in the early diagnosis of colorectal cancer and it teaches a kit for performing the method of the invention.
    • 本发明涉及一种协助评估结肠直肠癌的方法。 该方法特别用于评估体外存在或不存在结肠直肠癌。 该方法例如通过分析生物化学标记来实施,包括在粪便样品中测量血红蛋白/触珠蛋白复合物和钙卫蛋白的浓度,并将确定的浓度与不存在或存在结肠直肠癌相关联。 为了进一步改善基于本发明方法的结肠直肠癌的评估,可以在粪便样品中与血红蛋白/触珠蛋白复合物和钙卫蛋白一起测定一种或多种另外的标记物的水平,并与结肠直肠癌的存在或不存在相关 。 本发明还涉及包含血红蛋白/触珠蛋白复合物和钙卫蛋白的标记物在早期诊断结肠直肠癌中的用途,并且其教导了用于实施本发明方法的试剂盒。
    • 30. 发明申请
    • IGFBP-7 AS A MARKER IN PREECLAMPSIA
    • IGFBP-7作为前列腺炎的标志物
    • WO2017148854A1
    • 2017-09-08
    • PCT/EP2017/054484
    • 2017-02-27
    • ROCHE DIAGNOSTICS GMBHF. HOFFMANN-LA ROCHE AGROCHE DIAGNOSTICS OPERATIONS, INC.
    • HUND, MartinKAISER, Edelgard AnnaWIENHUES-THELEN, Ursula-HenrikeBLOCK, DirkKARL, Johann
    • G01N33/68G06F19/10
    • G01N33/689G01N33/6893G01N2333/4703G01N2333/4745G01N2800/368G01N2800/52G01N2800/60G16B99/00
    • The present invention relates to a method for diagnosing preeclampsia or a preeclampsia-related condition in a pregnant subject. The preeclampsia-related condition can be eclampsia, HELLP syndrome or proteinuria. Said method is based on the measurement of the amount of the biomarker IGFBP-7 (Insulin-like Growth Factor Binding Protein 7) in a sample from the subject and on the comparison of the measured amount to a reference. Also encompassed by the present invention are methods for assessing the severity of preeclampsia or a preeclampsia-related condition and methods for monitoring a preeclampsia or a preeclampsia-related condition in a pregnant subject. The present invention further relates to the use of the biomarker IGFBP-7 or of an agent that specifically binds to IGFBP-7 in a sample from a pregnant subject for diagnosing, for monitoring or for assessing the severity of preeclampsia or a preeclampsia-related condition. Optionally, sFlt-1, Endoglin, PIGF are determined. Finally, the present invention relates to a device adapted to carry out the method of the present invention.
    • 本发明涉及用于诊断怀孕受试者中先兆子痫或先兆子痫相关病症的方法。 先兆子痫相关病症可以是子痫,HELLP综合征或蛋白尿。 所述方法基于对来自受试者的样品中生物标志物IGFBP-7(胰岛素样生长因子结合蛋白7)的量的测量以及将测量量与参比进行比较。 本发明还包括用于评估先兆子痫或先兆子痫相关病症的严重程度的方法以及用于监测怀孕受试者中先兆子痫或先兆子痫相关病症的方法。 本发明进一步涉及生物标志物IGFBP-7或特异性结合来自怀孕受试者的样品中的IGFBP-7的试剂用于诊断,监测或评估先兆子痫或先兆子痫相关病症的严重程度 。 任选地,确定sFlt-1,内皮糖蛋白,PIGF。 最后,本发明涉及一种适于执行本发明方法的装置。