RAGE-related compositions
    1.
    发明申请
    RAGE-related compositions 审中-公开
    RAGE相关组合物

    公开(公告)号:US20050170382A1

    公开(公告)日:2005-08-04

    申请号:US10990310

    申请日:2004-11-15

    摘要: The present invention provides for an isolated human EN-RAGE peptide. The present invention also provides for a method for determining whether a compound is capable of inhibiting the interaction of an EN-RAGE peptide with a RAGE peptide, which comprises: (a) admixing: (i) a RAGE peptide or an sRAGE peptide or a fragment of either thereof, (ii) an EN-RAGE peptide or a fragment thereof, and (iii) the compound; (b) measuring the level of interaction between the peptide of step (a) (i) and the peptide of step (a) (ii), and (c) comparing the amount of interaction meausred in step (b) with the amount measured between the petpide of step (a) (i) and the peptide of step (a) (ii) in the absence of the compound, thereby determining whether the compound is capable of inhibiting the interaction of the EN-RAGE peptide with the RAGE peptide, wherein a reduction in the amount of interaction in the presence of the compound indicates that the compound is capable of inhibiting the interaction. The present invention also provides for a method for inhibiting inflammation in a subject which comprises administering to the subject a compound capable of interfering with the interaction between EN-RAGE peptide and receptor for advanced glycation endproduct (RAGE) in the subject thereby inhibiting inflammation in the subject.

    摘要翻译: 本发明提供了分离的人类EN-RAGE肽。 本发明还提供了一种用于确定化合物是否能够抑制EN-RAGE肽与RAGE肽的相互作用的方法,其包括:(a)混合:(i)RAGE肽或sRAGE肽或 片段,(ii)EN-RAGE肽或其片段,和(iii)化合物; (b)测量步骤(a)(i)的肽与步骤(a)(ii)的肽之间的相互作用水平,和(c)将步骤(b)中所发生的相互作用的量与测量的量进行比较 在不存在化合物的情况下,步骤(a)(i)的petpide和步骤(a)(ii)的肽之间,从而确定化合物是否能够抑制EN-RAGE肽与RAGE肽的相互作用 其中在化合物存在下相互作用量的减少表明该化合物能够抑制相互作用。 本发明还提供了一种抑制受试者的炎症的方法,其包括向受试者施用能够干扰受试者的EN-RAGE肽和受体之间相互作用的晚期糖基化终产物(RAGE)的相互作用,从而抑制受试者的炎症 学科。

    Methods of inhibiting binding of beta-sheet fibril to rage and consequences thereof
    2.
    发明申请
    Methods of inhibiting binding of beta-sheet fibril to rage and consequences thereof 审中-公开
    抑制β-片原纤维结合的愤怒及其后果的方法

    公开(公告)号:US20080019986A1

    公开(公告)日:2008-01-24

    申请号:US11805164

    申请日:2007-05-21

    IPC分类号: A61K38/00 A61K39/00

    摘要: This invention provides a method of inhibiting the binding of a β-sheet fibril to RAGE on the surface of a cell which comprises contacting the cell with a binding inhibiting amount of a compound capable of inhibiting binding of the β-sheet fibril to RAGE so as to thereby inhibit binding of the β-sheet fibril to RAGE. In one embodiment the β-sheet fibril is amyloid fibril. In one embodiment, the compound is sRAGE or a fragment thereof. In another embodiment, the compound is an anti-RAGE antibody or portion thereof. This invention provides the above method wherein the inhibition of binding of the β-sheet fibril to RAGE has the consequences of decreasing the load of β-sheet fibril in the tissue, inhibiting fibril-induced programmed cell death, inhibiting fibril-induced cell stress. This invention also provides methods of determining whether a compound inhibits binding of a β-sheet fibril to RAGE on the surface of a cell.

    摘要翻译: 本发明提供了抑制细胞表面上的β-片原纤维与RAGE的结合的方法,其包括使细胞与结合抑制量的能够抑制β-片原纤维结合的化合物与RAGE接触,以便 从而抑制β-片原纤维与RAGE的结合。 在一个实施方案中,β-片原纤维是淀粉样蛋白原纤维。 在一个实施方案中,化合物是sRAGE或其片段。 在另一个实施方案中,化合物是抗RAGE抗体或其部分。 本发明提供了上述方法,其中抑制β-片原纤维与RAGE的结合具有降低组织中β-片原纤维的负荷,抑制原纤维诱导的程序性细胞死亡,抑制原纤维诱导的细胞应激的后果。 本发明还提供了确定化合物是否抑制β片原纤维与细胞表面上的RAGE结合的方法。

    Ligand binding site of rage and uses thereof
    3.
    发明授权
    Ligand binding site of rage and uses thereof 失效
    配体结合位点及其用途

    公开(公告)号:US06555651B2

    公开(公告)日:2003-04-29

    申请号:US08948131

    申请日:1997-10-09

    IPC分类号: A61K3800

    摘要: The present method provides for an isolated peptide having an amino acid sequence corresponding to the amino acid sequence of a V-domain of a receptor for advanced glycation endproduct (RAGE). The present invention also provides for an isolated peptide having an amino acid sequence A-Q-N-I-T-A-R-I-G-E-P-L-V-L-K-C-K-G-A-P-K-K-P-P-Q-R-L-E-W-K (SEQ. ID No: 1). The present invention provides for a pharmaceutical composition comprising a therapeutically effect amount of an isolated peptide having an amino acid sequence corresponding to the amino acid sequence of a V-domain of RAGE. The present invention also provides for a method for inhibiting interaction of an amyloid-&bgr; peptide with a receptor for advanced glycation end product which is on the surface of a cell, which comprises contacting the cell with the peptide or a functionally equivalent agent, wherein the peptide or agent is capable of inhibiting interaction of the amyloid-&bgr; peptide with the receptor for advanced glycation end product, and the peptide or agent is present in an amount effective to inhibit interaction of the amyloid-&bgr; peptide with the receptor for advanced glycation endproduct.

    摘要翻译: 本方法提供了具有对应于晚期糖基化终产物(RAGE)受体的V-结构域的氨基酸序列的氨基酸序列的分离的肽。 本发明还提供具有氨基酸序列A-Q-N-I-T-A-R-I-G-E-P-L-V-L-K-C-K-G-A-P-K-P-P-Q-R-L-E-W-K(SEQ ID NO:1)的分离肽。 本发明提供了一种药物组合物,其包含治疗有效量的具有对应于RAGE的V-结构域的氨基酸序列的氨基酸序列的分离的肽。 本发明还提供了抑制淀粉样蛋白-β肽与细胞表面上的晚期糖基化终产物的受体的相互作用的方法,其包括使细胞与肽或功能等同试剂接触,其中 肽或试剂能够抑制淀粉样蛋白β肽与晚期糖基化终产物的受体的相互作用,并且肽或试剂以有效抑制淀粉样蛋白-β肽与晚期糖基化终产物受体相互作用的量存在 。

    Methods for treating multiple sclerosis
    4.
    发明申请
    Methods for treating multiple sclerosis 审中-公开
    治疗多发性硬化症的方法

    公开(公告)号:US20070167360A1

    公开(公告)日:2007-07-19

    申请号:US10577506

    申请日:2004-10-28

    申请人: Shi Yan David Stern

    发明人: Shi Yan David Stern

    IPC分类号: A61K38/17

    CPC分类号: A61K31/00 A61K38/1774

    摘要: This invention provides a method for treating a subject afflicted with multiple sclerosis comprising administering to the subject a therapeutically effective amount of soluble receptor for advanced glycation endproducts (sRAGE). This invention further provides a method for inhibiting CD4+ T-cell migration comprising contacting the CD4+ T-cell with soluble receptor for advanced glycation endproducts (sRAGE). This invention further provides a method for inhibiting chemokine receptor activation in a subject comprising administering to the subject a therapeutically effective amount of soluble receptor for advanced glycation endproducts (sRAGE).

    摘要翻译: 本发明提供了治疗患有多发性硬化症的受试者的方法,其包括向受试者施用治疗有效量的晚期糖基化终产物(sRAGE)的可溶性受体。 本发明进一步提供了一种抑制CD4 + T细胞迁移的方法,包括使CD4 + T细胞与晚期糖基化终产物(sRAGE)的可溶性受体接触。 本发明进一步提供了一种用于抑制受试者中趋化因子受体活化的方法,包括向受试者施用治疗有效量的晚期糖基化终产物(sRAGE)的可溶性受体。

    Method to prevent accelerated atherosclerosis using (sRAGE) soluble receptor for advanced glycation endproducts
    5.
    发明申请
    Method to prevent accelerated atherosclerosis using (sRAGE) soluble receptor for advanced glycation endproducts 失效
    使用(sRAGE)可溶性受体预防晚期糖基化终末产物预防加速动脉粥样硬化的方法

    公开(公告)号:US20070099829A1

    公开(公告)日:2007-05-03

    申请号:US11319949

    申请日:2005-12-27

    IPC分类号: A61K38/17

    摘要: The present invention provides for a method to prevent accelerated atherosclerosis in a subject predisposed thereto which comprises administering to the subject a polypeptide derived from soluble receptor for advanced glycation endproduct in an amount effective to prevent accelerated atherosclerosis in the subject. The present invention also provides for a method to prevent a macrovessel disease in a subject predisposed thereto which comprises administering to the subject a polypeptide derived from soluble receptor for advanced glycation endproduct in an amount effective to prevent macrovessel disease in the subject.

    摘要翻译: 本发明提供了预防易感患者的加速动脉粥样硬化的方法,其包括以有效预防受试者加速的动脉粥样硬化的量向受试者施用衍生自可溶性受体的晚期糖基化终产物的多肽。 本发明还提供一种预防患者易患有大血管疾病的方法,其包括以有效预防受试者的宏观血管疾病的量向受试者施用衍生自可溶性受体的晚期糖基化终产物的多肽。

    Methods for treating an ischemic disorder and improving stroke outcome
    6.
    发明申请
    Methods for treating an ischemic disorder and improving stroke outcome 审中-公开
    治疗缺血性疾病和改善中风结局的方法

    公开(公告)号:US20050250688A1

    公开(公告)日:2005-11-10

    申请号:US10692439

    申请日:2003-10-22

    CPC分类号: A61K38/4846

    摘要: The present invention provides for a method for treating an ischemic disorder in a subject which comprises administering to the subject a pharmaceutically acceptable Factor IXa compound in a sufficient amount over a sufficient time period so as to treat the ischemic disorder in the subject. The invention further provides a method for treating an ischemic disorder in a subject which comprises administering to the subject a pharmaceutically acceptable form of inactivated Factor IXa in a sufficient amount over a sufficient period of time to inhibit coagulation so as to treat the ischemic disorder in the subject.

    摘要翻译: 本发明提供一种治疗受试者的缺血性疾病的方法,其包括在足够的时间内向受试者施用足够量的药学上可接受的因子IXa化合物,以治疗受试者的缺血性疾病。 本发明还提供了一种治疗受试者的缺血性疾病的方法,其包括在足够的时间内以足够的时间向受试者施用药学上可接受的形式的灭活因子IXa以抑制凝血,以便治疗缺血性疾病 学科。

    METHOD AND APPARATUS FOR CUSTOMIZED PROVISIONING OF ON-LINE APPLICATION CHANNELS
    8.
    发明申请
    METHOD AND APPARATUS FOR CUSTOMIZED PROVISIONING OF ON-LINE APPLICATION CHANNELS 有权
    定制提供在线应用通道的方法和装置

    公开(公告)号:US20130018938A1

    公开(公告)日:2013-01-17

    申请号:US13180375

    申请日:2011-07-11

    IPC分类号: G06F15/16

    摘要: A method for a computer system includes receiving an identifier associated with a client streaming player, determining one or more attributes associated with the identifier from a data structure in response to the identifier, determining available channels from a plurality of channels that are to be made available to the client streaming player in response to the identifier, wherein available channels comprises a first channel, but not the second channel, determining a first graphical identifier associated with the first channel, providing the first graphical identifier to the client streaming player, receiving a user selection of the first graphical identifier indicating a user request to associate the first channel with the computer system, and providing an indicator of a server network address associated with the first channel to the client streaming player.

    摘要翻译: 一种用于计算机系统的方法包括:接收与客户端流播放器相关联的标识符,响应于所述标识符从数据结构确定与所述标识符相关联的一个或多个属性,从多个信道中确定可用信道 响应于所述标识符到所述客户端流播放器,其中可用信道包括第一信道而不是所述第二信道,确定与所述第一信道相关联的第一图形标识符,向所述客户端流播放器提供所述第一图形标识符,接收用户 选择第一图形标识符,指示用户请求将第一频道与计算机系统相关联,以及向客户端流播放器提供与第一频道相关联的服务器网络地址的指示符。

    METHODS AND DEVICES FOR READING MICROARRAYS
    9.
    发明申请
    METHODS AND DEVICES FOR READING MICROARRAYS 有权
    读取微阵列的方法和设备

    公开(公告)号:US20100296727A1

    公开(公告)日:2010-11-25

    申请号:US12780825

    申请日:2010-05-14

    IPC分类号: G06K9/00 B23P11/00

    摘要: In one embodiment of the invention, a method to image a probe array is described that includes focusing on a plurality of fiducials on a surface of an array. The method utilizes obtaining the best z position of the fiducials and using a surface fitting algorithm to produce a surface fit profile. One or more surface non-flatness parameters can be adjusted to improve the flatness image of the array surface to be imaged.

    摘要翻译: 在本发明的一个实施例中,描述了一种对探针阵列成像的方法,其包括聚焦在阵列表面上的多个基准点上。 该方法利用获得基准的最佳z位置并使用表面拟合算法来产生表面拟合曲线。 可以调整一个或多个表面非平坦度参数以改善待成像的阵列表面的平坦度图像。

    Implantable wireless sensor for pressure measurement within the heart
    10.
    发明授权
    Implantable wireless sensor for pressure measurement within the heart 有权
    可植入无线传感器,用于心脏内的压力测量

    公开(公告)号:US07481771B2

    公开(公告)日:2009-01-27

    申请号:US10886829

    申请日:2004-07-07

    IPC分类号: A61B5/0215

    CPC分类号: A61B5/0031 A61B5/0215

    摘要: The progress of a endovascular cardiac repair can be monitored by inserting a pressure transducer sensor using a catheter into a chamber of the heart during endovascular repair and then using a small, hand-held read out device to measure pressure easily, safely, inexpensively and accurately. In one aspect a sensor is introduced into the body by the steps of folding or rolling the sensor into a cylinder, loading it into a catheter, and deploying into the heart chamber by allowing it to unroll or unfold, either by itself or facilitated by the incorporation of a super-elastic alloy component.

    摘要翻译: 可以通过在血管内修复期间使用导管将压力换能器传感器插入心脏腔室来监测血管内心脏修复的进展,然后使用小的手持式读出装置来容易地,安全地,低成本地和准确地测量压力 。 在一个方面,传感器通过将传感器折叠或滚动到圆筒中,将其装入导管中并通过允许其自身展开或展开而部署到心室中的步骤被引入到体内, 掺入超弹性合金成分。