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    • 5. 发明申请
    • TREATMENT OF CHRONIC PAIN ASSOCIATED WITH DRUG OR RADIATION THERAPY
    • 治疗与药物或放射治疗相关的慢性疼痛
    • WO2004105690A3
    • 2005-03-10
    • PCT/US2004016101
    • 2004-05-20
    • CYPRESS BIOSCIENCE INCRAO SRINIVAS GKRANZLER JAY D
    • RAO SRINIVAS GKRANZLER JAY D
    • A61K20060101A61K31/137A61K31/22A61K31/55
    • A61K31/22
    • Methods for treating chronic widespread pain associated with drug therapy or radiation therapy are described. The method generally involves administering a therapeutically effective amount of a dual or tri reuptake inhibitor of a specific type or a pharmaceutically acceptable salt thereof. Preferably the compound is a non-tricyclic dual reuptake inhibitor. The most preferred compound is milnacipran or a bioequivalent or pharmaceutically acceptable salt thereof. Other preferred compounds are duloxetine and venlafaxine or a bioequivalent or pharmaceutically acceptable salt thereof. In yet another embodiment, a therapeutically effective amount of a non-tricyclic triple reuptake inhibitor ("TRI") compound of a specific type, or a pharmaceutically acceptable salt thereof, is administered. The TRI compounds are characterized by their ability to block the reuptake (and, hence, increase central concentrations of) the three primary brain monoamines: serotonin, noradrenaline, and dopamine.
    • 描述了治疗与药物治疗或放射治疗相关的慢性广泛疼痛的方法。 该方法通常涉及给予治疗有效量的特异型或其可药用盐的双重或三次再摄取抑制剂。 优选地,该化合物是非三环双重再摄取抑制剂。 最优选的化合物是米那普仑或其生物等效或药学上可接受的盐。 其他优选的化合物是度洛西汀和文拉法辛或其生物等效或药学上可接受的盐。 在另一个实施方案中,施用治疗有效量的特定类型的非三环三重再摄取抑制剂(“TRI”)化合物或其药学上可接受的盐。 TRI化合物的特征在于其阻断三种主要脑单胺(5-羟色胺,去甲肾上腺素和多巴胺)的再摄取(并因此增加中心浓度)的能力。
    • 6. 发明申请
    • METHOD AND SYSTEM FOR CREATING SEAMLESS NARRATED VIDEOS USING REAL TIME STREAMING MEDIA
    • 使用实时流媒体创建无缝NARRATED视频的方法和系统
    • WO2016118537A1
    • 2016-07-28
    • PCT/US2016/013976
    • 2016-01-19
    • RAO, Srinivas
    • RAO, Srinivas
    • H04N7/173
    • H04N21/47205G06F3/0482G06F9/451G06F2203/04803H04L65/60H04N21/4307H04N21/4622H04N21/47217H04N21/4782H04N21/4884
    • A computer-implemented method and system for creating a streaming media compilation having time-synchronized annotations. The computer-implemented method includes accessing streaming media from one or more external sources through a browser user interface. Further, the computer-implemented method includes passing a particular Nr8 to two entities to a requesting browser and tagging and annotating the streaming media. Furthermore, the computer-implemented method includes mapping the annotations to a master time-line thereby providing a single seamless video experience of one single media presentation wherein the user performs a desired action, the action includes one of play, pause, seek and scroll. Moreover, the computer-implemented method includes displaying a top panel and a bottom panel to a user through a Nr8 user interface.
    • 一种用于创建具有时间同步注释的流媒体汇编的计算机实现的方法和系统。 计算机实现的方法包括通过浏览器用户界面从一个或多个外部源访问流媒体。 此外,计算机实现的方法包括将特定Nr8传递给两个实体到请求浏览器,并标记和注释流媒体。 此外,计算机实现的方法包括将注释映射到主时间线,从而提供单个媒体呈现的单个无缝视频体验,其中用户执行期望的动作,该动作包括播放,暂停,寻找和滚动之一。 此外,计算机实现的方法包括通过Nr8用户界面向用户显示顶板和底板。
    • 7. 发明申请
    • ? NOVEL MECHANISM TO ENGAGE GEARS IN MOTION
    • ? 在运动中接触齿轮的新机制
    • WO2009087654A3
    • 2009-12-03
    • PCT/IN2008000702
    • 2008-10-24
    • MAHINDRA AND MAHINDRAGILL SANJAYADIGA GANESHRAO SRINIVAS K V VRANADE NITIN SHANKAR
    • GILL SANJAYADIGA GANESHRAO SRINIVAS K V VRANADE NITIN SHANKAR
    • G05G5/08
    • F16H63/302
    • The invention comprises a reverse gear engagement mechanism that engages reverse gear effectively and while minimizing the reverse gear wear and tear and the noise level. It works by reducing the speed of reverse idler gear to a level required for reverse gear engagement, before engaging with the idler fixed gear. The invention can be installed on new and existing automobiles that have manual gearboxes. The mechanism used for the speed reduction comprises specially designed and located friction elements that reduce the speeds of axial and rotational motions of the idler reverse gear. The axial and rotational speeds are reduced to a range where the idler reverse gear engages with the fixed reverse gear smoothly, thereby causing minimal noise and wear and tear of the engaging parts.
    • 本发明包括倒档接合机构,该倒档接合机构有效地接合倒档并且同时最小化倒档磨损和噪音水平。 在与惰轮固定齿轮接合之前,它通过将倒档惰轮的速度降低至倒档接合所需的水平来工作。 本发明可以安装在具有手动变速箱的新的和现有的汽车上。 用于减速的机构包括专门设计和定位的摩擦元件,其减小惰轮倒档的轴向和旋转运动的速度。 轴向转速和转速减小到惰轮倒档齿轮与固定倒档齿轮平滑啮合的范围,由此导致啮合部分的噪音和磨损最小。
    • 9. 发明申请
    • INFLUENZ DNA VACCINATION AND METHODS OF USE THEREOF
    • INFLUENZ DNA疫苗及其使用方法
    • WO2009092038A1
    • 2009-07-23
    • PCT/US2009031329
    • 2009-01-16
    • US GOV HEALTH & HUMAN SERVRAO SRINIVASNABEL GARY JYANG ZIH-YONGWEI CHIH-JENKONG WING-PUI
    • RAO SRINIVASNABEL GARY JYANG ZIH-YONGWEI CHIH-JENKONG WING-PUI
    • A61K39/145
    • A61K39/145A61K39/12A61K2039/53A61K2039/54A61K2039/58A61K2039/70C07K14/005C12N2760/16122C12N2760/16134
    • Sustained outbreaks of highly pathogenic avian influenza (HPAI) H5N1 in avian species increase the risk of reassortment and adaptation to humans. The ability to contain its spread in birds would reduce this threat and help maintain the capacity for egg-based vaccine production. While vaccines offer the potential to control avian disease, a major concern of current vaccines is their inability to protect against evolving avian influenza viruses. DNA vaccines encoding hemagglutinin (HA) proteins from different HPAI H5N1 serotypes protect against homologous and heterologous HPAI H5N1 strain challenge in animals. These vaccines elicit antibodies that neutralize multiple serotypes of HPAI H5N1 when given in combinations containing up to 10 HAs. The response is dose-dependent. The breadth of protection is determined by the choice of the influenza virus HA in the vaccine. Monovalent and trivalent HA immunogens and/or vaccines conferred complete protection in mice against lethal H5N1 A/Vietnam/ 1203/2004 challenge 68 weeks after vaccination. In chickens, complete protection was conferred against heterologous strains of HPAI H5N1 after vaccination with a trivalent H5 serotype DNA vaccine with doses as low as 5 µg DNA given twice either by intramuscular needle injection or with a needle-free device.
    • 高致病性禽流感(HPAI)H5N1在禽类物种中的持续爆发增加了重配和适应人类的风险。 控制其在鸟类中传播的能力将减少这种威胁,并有助于维持基于蛋的疫苗生产的能力。 虽然疫苗具有控制禽流感病毒的潜力,但目前疫苗的主要问题是其无法防止禽流感病毒进化。 编码来自不同HPAI H5N1血清型的血凝素(HA)蛋白质的DNA疫苗保护动物免受同源和异源HPAI H5N1毒株攻击。 当以最多10HA的组合给予时,这些疫苗引发中和多种血清型的HPAI H5N1的抗体。 反应是剂量依赖性的。 保护的广度由疫苗中流感病毒HA的选择决定。 疫苗接种后68周,单价和三价HA免疫原和/或疫苗在小鼠中完全保护免于致死的H5N1 A /越南/ 1203/2004攻击。 在鸡中,用三价H5血清型DNA疫苗接种后,通过肌内注射或无针装置给予两次,剂量低至5μg的DNA,对抗HPAI H5N1的异源菌株进行完全保护。