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    • 44. 发明授权
    • Methods, devices and kits for detecting or monitoring acute kidney injury
    • 用于检测或监测急性肾损伤的方法,装置和试剂盒
    • US09476880B2
    • 2016-10-25
    • US13130456
    • 2009-11-23
    • Per Venge
    • Per Venge
    • G01N33/543G01N33/573
    • G01N33/573G01N2800/347
    • Methods for detecting acute kidney injury in an individual comprise (a) contacting a body fluid sample from the individual with an assay device including neutrophil gelatinase-associated lipocalin (NGAL) antibody and a detectable label, to allow complexing of NGAL protein in the sample with NGAL antibody, and determining an amount of complex formed between NGAL protein from the sample and NGAL antibody in the assay device using the detectable label, wherein NGAL antibody in the device has binding capacity with more than two NGAL protein epitopes, and wherein the amount of the formed complex represents a level of acute kidney injury. Methods for determining an origin of NGAL protein in a sample from an individual include the step of determining relative amounts of monomeric, dimeric and heterodimeric forms of NGAL protein in the sample and allow improved diagnosis and therefore better targeted treatment.
    • 用于检测个体中急性肾损伤的方法包括(a)使来自个体的体液样品与包括嗜中性粒细胞明胶酶相关的脂质运载蛋白(NGAL)抗体和可检测标记的测定装置接触,以使样品中的NGAL蛋白质与 NGAL抗体,并且使用所述可检测标记确定所述样品中的NGAL蛋白质与所述测定装置中的NGAL抗体之间形成的复合物的量,其中所述装置中的NGAL抗体具有与两个以上NGAL蛋白质表位的结合能力,并且其中 形成的复合体代表急性肾损伤的水平。 用于确定来自个体的样品中NGAL蛋白来源的方法包括确定样品中NGAL蛋白的单体,二聚体和异二聚体形式的相对量的步骤,并允许改进的诊断并因此进行更好的靶向治疗。
    • 46. 发明授权
    • Externally connected time port changeover method and device
    • 外部连接的时间端口切换方式和设备
    • US09325442B2
    • 2016-04-26
    • US14116393
    • 2012-03-20
    • Xiaoxia LiHailiang Zhan
    • Xiaoxia LiHailiang Zhan
    • H04J3/06H04L12/24H04L12/40
    • H04J3/0638H04J3/0641H04J3/0644H04J3/0658H04L12/40176H04L41/0654
    • Disclosed are externally connected time port changeover method and device. The method includes: a node serving as a GM node transmitting time information via a first externally connected time port of the node; if the first externally connected time port fails, the node updating current node priority and GM node priority of the node as preset node priority which is node priority configured for the node when the node is activated; and the node judging whether a second externally connected time port of the node is up and the priority of the second externally connected time port is higher than the current GM node priority, if so, activating the second externally connected time port to transmit the time information. The problem that when the currently selected time access port has failed, changeover among ports cannot be completed in time is solved, thus improving the stability of the time synchronization network.
    • 公开了外部连接的时间端口切换方法和装置。 该方法包括:作为GM节点的节点经由节点的第一外部连接的时间端口发送时间信息; 如果第一个外部连接的时间端口出现故障,节点将该节点的当前节点优先级和GM节点优先级更新为预定节点优先级,该节点优先级是节点激活时为该节点配置的节点优先级; 并且所述节点判断所述节点的第二外部连接时间端口是否up,并且所述第二外部连接时间端口的优先级高于当前GM节点优先级,如果是,则激活所述第二外部连接的时间端口以发送所述时间信息 。 当当前选定的时间接入端口出现故障时,端口间的切换无法及时完成,从而提高了时间同步网络的稳定性。
    • 47. 发明授权
    • Antibodies and vaccines for use in therapeutic and diagnostic methods for α-synuclein-related disorders
    • 用于α-突触核蛋白相关疾病的治疗和诊断方法的抗体和疫苗
    • US09315569B2
    • 2016-04-19
    • US14336634
    • 2014-07-21
    • BioArctic Neuroscience AB
    • Lars LannfeltJoakim BergströmMartin IngelssonPär Gellerfors
    • C07K16/18A61K39/395G01N33/68A61K38/17
    • A61K51/1018A61K38/1709C07K16/18C07K2317/92G01N33/6896G01N2333/4709Y10S530/839
    • Methods of treating or delaying onset of a neurodegenerative disorder with α-synuclein pathology in an individual comprise administering an antibody which is produced from a stabilized soluble α-synuclein oligomer and capable of binding a stabilized soluble α-synuclein oligomer, the stabilized soluble α-synuclein oligomer having a lower formation rate to a non-soluble aggregated form than a non-stabilized soluble oligomer of the α-synuclein. The antibody has been collected from a non-human animal to which stabilized soluble α-synuclein oligomer had been administered or has been produced by hybridoma technology, phage display, ribosome display, mammalian cell display or bacterial display, and the disorder with α-synuclein pathology is characterized by deposition of Lewy bodies and Lewy neurites or is selected from the group consisting of Parkinson's disease (PD), dementia with Lewy bodies (DLB), the Lewy body variant of Alzheimer's disease, and multiple system atrophy (MSA).
    • 在个体中用α-突触核蛋白病理学治疗或延缓神经变性疾病发作的方法包括施用由稳定的可溶性α-突触核蛋白寡聚物产生并能够结合稳定的可溶性α-突触核蛋白寡聚体的稳定的可溶性α- 具有比非稳定的α-突触核蛋白可溶性低聚物低的形成速率与非可溶性聚集形式的突触核蛋白寡聚物。 已经从已经施用稳定的可溶性α-突触核蛋白寡聚体的非人动物收集抗体,或已经通过杂交瘤技术,噬菌体展示,核糖体展示,哺乳动物细胞展示或细菌展示以及α-突触核蛋白的病症产生抗体 病理学特征在于路易体和路易体神经突的沉积,或选自帕金森病(PD),路易体痴呆(DLB),阿尔茨海默病的路易体变体和多系统萎缩(MSA)。
    • 50. 发明授权
    • Surgical device
    • 手术装置
    • US09265486B2
    • 2016-02-23
    • US13586737
    • 2012-08-15
    • James David Hughett, Sr.Keith Edward MartinSalvatore Privitera
    • James David Hughett, Sr.Keith Edward MartinSalvatore Privitera
    • A61B17/04A61B17/00A61B17/122A61B17/128
    • A61B17/10A61B17/00A61B17/00234A61B17/083A61B17/1227A61B17/1285A61B2017/00367
    • A medical instrument comprising: (A) a first joint comprising a first member and a second member, the first member configured to be repositionable with respect to the second member in an X-Y plane; (B) a second joint operatively coupled to the first joint, the second joint comprising a third member and a fourth member, the third member configured to be repositionable with respect to the fourth member in a Y-Z plane perpendicular to the X-Y plane; and, (C) a controller operatively coupled to the first joint and the second joint, the controller including a first control configured to direct repositioning of at least one of the first member and the second member, and a second control configured to direct repositioning of at least one of the third member and the fourth member.
    • 一种医疗器械,包括:(A)包括第一构件和第二构件的第一接头,所述第一构件构造成在X-Y平面中可相对于所述第二构件重新定位; (B)可操作地联接到所述第一接头的第二接头,所述第二接头包括第三部件和第四部件,所述第三部件被配置为在垂直于所述X-Y平面的Y-Z平面中相对于所述第四部件重新定位; 和(C)可操作地联接到第一关节和第二关节的控制器,所述控制器包括构造成引导重新定位所述第一构件和所述第二构件中的至少一个的第一控制,以及第二控制,所述第二控制被配置为直接重新定位 第三成员和第四成员中的至少一个。