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    • 2. 发明申请
    • ELECTRICAL NERVE STIMULATION DEVICE
    • 电刺激装置
    • WO2005105201A3
    • 2006-01-19
    • PCT/GB2005001647
    • 2005-04-29
    • ALGOTEC LTDDANIELS SUSAN ROMAO-DUARTE
    • DANIELS SUSAN ROMAO-DUARTE
    • A61N1/05A61N1/34A61N1/36A61N1/372
    • A61N1/0551A61N1/025A61N1/36071A61N1/37211
    • An electrical nerve stimulation device (500) has an electrode lead (502) and pulse generator (504) connected to one another and sealed in a fluid impermeable housing (526) to form a single sealed unit. The housing (526) is generally flat and both the electrode lead (502) and the pulse generator (504) are substantially flexible. Electrodes (516) are positioned along the length of the lead (502). Each electrode (516) comprises a group of electrical contacts spaced apart from one another along the length of the lead (502) so that the electrodes (516) can also be generally flexible. The distance along the lead (502) between the pulse generator (504) and the electrode (516) closest to the pulse generator (504) is less than around 5 cm. The electrodes (516) each extend along the length of the lead (502) for around 2 cm or more. The electrode lead (502) has an electronically readable memory for storing information about the lead (502), which can be read by the pulse generator (504). The pulse generator (504) can deliver pulses of electrical potential between the electrodes (516). The device (500) can be implanted in a human or animal body and used for treatments such as subcutaneous electrical nerve stimulation (SENS).
    • 电神经刺激装置(500)具有彼此连接并密封在流体不可渗透壳体(526)中以形成单个密封单元的电极引线(502)和脉冲发生器(504)。 外壳(526)通常是平坦的,电极引线(502)和脉冲发生器(504)都基本上是柔性的。 电极(516)沿引线(502)的长度定位。 每个电极(516)包括沿引线(502)的长度彼此间隔开的一组电触头,使得电极(516)也可以是大致柔性的。 脉冲发生器(504)和最接近脉冲发生器(504)的电极(516)之间的引线(502)的距离小于约5cm。 电极(516)各自沿着引线(502)的长度延伸约2cm或更大。 电极引线(502)具有用于存储关于引线(502)的信息的电子可读存储器,其可由脉冲发生器(504)读取。 脉冲发生器(504)可以在电极(516)之间传递电位脉冲。 装置(500)可植入人体或动物体内,用于皮下电神经刺激(SENS)等治疗。
    • 9. 发明申请
    • PREDICTIVE MODELS AND METHODS FOR DIAGNOSING AND ASSESSING CORONARY ARTERY DISEASE
    • 预测模型和方法诊断和评估冠状动脉疾病
    • WO2009049257A9
    • 2009-10-29
    • PCT/US2008079646
    • 2008-10-10
    • CARDIO DX INCROSENBERG STEVEDANIELS SUSANELASHOFF MICHAEL RWINGROVE JAMES ATINGLEY WHITTEMORE GSEHNEERT AMY JPAONI NICHOLAS F
    • ROSENBERG STEVEDANIELS SUSANELASHOFF MICHAEL RWINGROVE JAMES ATINGLEY WHITTEMORE GSEHNEERT AMY JPAONI NICHOLAS F
    • C12Q1/68
    • C12Q1/6883C12Q2600/112C12Q2600/158
    • Biomarkers useful for diagnosing and assessing the extent of coronary artery disease (CAD) are provided, along with kits for measuring their expression. The invention also provides predictive models, based on the biomarkers, as well as computer systems, and software embodiments of the models for scoring and optionally classifying samples. In a preferred embodiment, the biomarkers are organized into clustered groups. The expression level of the biomarkers within a group are highly correlated to each other in normal and disease states. Expression values of genes chosen from each of two, three, four or five of the clustered gene groups, A, B, C, D, E may be used. Alternatively, expression values of genes chosen from the groups are combined into a metagene. Preferred biomarkers include S100A12, S100A8, S100A9, BCL2A1, and F5 (group A); XK, P62, and FECH (group B); TUBB2 (group C); IFNG, PDGFB, VSIG4, and TNF (group D); CSF3R, TLR5, CD46, and NCFl (group E); S100A12, S100A9, BCL2A1, TXN and CSTA (group I); OLIGl, 0LIG2, AD0RA3, CLC, and SLC29A1 (group II); and CBS and ARGl (group IV).
    • 提供用于诊断和评估冠状动脉疾病(CAD)程度的生物标志物,以及用于测量其表达的试剂盒。 本发明还提供了基于生物标志物的预测模型以及计算机系统和用于对样品进行评分和任选分类的模型的软件实施例。 在一个优选的实施方案中,生物标志物被组织成群集。 组内生物标志物的表达水平在正常和疾病状态下彼此高度相关。 可以使用从2,3,4或5个群集基因组A,B,C,D,E中的每一个中选择的基因的表达值。 或者,将选自这些基因的基因的表达值组合成一种变应原。 优选的生物标志物包括S100A12,S100A8,S100A9,BCL2A1和F5(A组); XK,P62和FECH(B组); TUBB2(C组); IFNG,PDGFB,VSIG4和TNF(D组); CSF3R,TLR5,CD46和NCF1(E组); S100A12,S100A9,BCL2A1,TXN和CSTA(组I); OLIG1,0LIG2,AD0RA3,CLC和SLC29A1(组II); 和CBS和ARG1(第IV组)。
    • 10. 发明申请
    • PREDICTIVE MODELS AND METHODS FOR DIAGNOSING AND ASSESSING CORONARY ARTERY DISEASE
    • 用于诊断和评估冠状动脉疾病的预测模型和方法
    • WO2009049257A3
    • 2009-07-02
    • PCT/US2008079646
    • 2008-10-10
    • CARDIO DX INCROSENBERG STEVEDANIELS SUSANELASHOFF MICHAEL RWINGROVE JAMES ATINGLEY WHITTEMORE GSEHNEERT AMY JPAONI NICHOLAS F
    • ROSENBERG STEVEDANIELS SUSANELASHOFF MICHAEL RWINGROVE JAMES ATINGLEY WHITTEMORE GSEHNEERT AMY JPAONI NICHOLAS F
    • C12Q1/68
    • C12Q1/6883C12Q2600/112C12Q2600/158
    • Biomarkers useful for diagnosing and assessing the extent of coronary artery disease (CAD) are provided, along with kits for measuring their expression. The invention also provides predictive models, based on the biomarkers, as well as computer systems, and software embodiments of the models for scoring and optionally classifying samples. In a preferred embodiment, the biomarkers are organized into clustered groups. The expression level of the biomarkers within a group are highly correlated to each other in normal and disease states. Expression values of genes chosen from each of two, three, four or five of the clustered gene groups, A, B, C, D, E may be used. Alternatively, expression values of genes chosen from the groups are combined into a metagene. Preferred biomarkers include S100A12, S100A8, S100A9, BCL2A1, and F5 (group A); XK, P62, and FECH (group B); TUBB2 (group C); IFNG, PDGFB, VSIG4, and TNF (group D); CSF3R, TLR5, CD46, and NCFl (group E); S100A12, S100A9, BCL2A1, TXN and CSTA (group I); OLIGl, 0LIG2, AD0RA3, CLC, and SLC29A1 (group II); and CBS and ARGl (group IV).
    • 提供了有助于诊断和评估冠状动脉疾病(CAD)程度的生物标志物,以及用于测量其表达的试剂盒。 本发明还提供了基于生物标志物的预测模型,以及用于评分和可选地分类样品的模型的计算机系统和软件实施方案。 在优选的实施方案中,生物标志物被组织成聚集的组。 一组中生物标志物的表达水平在正常和疾病状态下彼此高度相关。 可以使用从两个,三个,四个或五个聚簇基因组A,B,C,D,E中的每一个中选择的基因的表达值。 或者,选自组中的基因的表达值被组合成元源。 优选的生物标志物包括S100A12,S100A8,S100A9,BCL2A1和F5(组A); XK,P62和FECH(B组); TUBB2(C组); IFNG,PDGFB,VSIG4和TNF(D组); CSF3R,TLR5,CD46和NCF1(组E); S100A12,S100A9,BCL2A1,TXN和CSTA(组I); OLIG1,0LIG2,AD0RA3,CLC和SLC29A1(组II); 和CBS和ARG1(组IV)。